3586 Biotechnology Jobs - Page 14

Job Title: Flow Cytometrist – QC (Quality Control) Location: Vapi, Gujarat Employment Type: Full-time About the Role: We are seeking a highly skilled and detail-oriented Flow Cytometrist to join our Quality Control team at our state-of-the-art life sciences facility in Vapi. The ideal candidate will be responsible for performing flow cytometry analyses, ensuring compliance with quality standards, and supporting the release of critical biological products. Key Responsibilities: Perform flow cytometry assays to assess cell populations, viability, immunophenotyping, and other QC parameters. Prepare and handle samples, reagents, and controls in accordance with GMP/GLP guidelines. Operate, calibrate, and maintain flow cytometers (BD, Beckman Coulter, or similar platforms). Analyze data using flow cytometry software (FlowJo, FCS Express, etc.) and generate detailed QC reports. Develop, optimize, and validate flow cytometry-based analytical methods for new products. Support troubleshooting , instrument qualification (IQ/OQ/PQ), and routine maintenance. Collaborate with cross-functional teams including QA, R&D, and manufacturing to ensure product quality. Ensure compliance with regulatory standards (FDA, EMA, ISO, ICH) and maintain proper documentation. Train and mentor junior staff on flow cytometry techniques and QC processes. Qualifications & Experience: Master’s degree (M.Sc) or PhD in Life Sciences , Biotechnology, Microbiology, Immunology, or related field. 3–5 years of hands-on experience in flow cytometry within a QC/QA/biologics Strong understanding of GMP/GLP and regulatory requirements. Proficiency in flow cytometry software and data interpretation. Excellent analytical, documentation, and problem-solving skills. Ability to work effectively in a fast-paced, team-oriented environment. Preferred Skills: Experience with cell-based assays , immunoassays, and cytometric bead arrays. Knowledge of quality management systems (QMS) and audit processes. Familiarity with sterile techniques and biosafety practices.

YOUR RESPONSIBILITIES Develop and deliver course content, including assessments and academic questions, for engineering students Create interactive learning resources and simulations To plan deliverables to meet the timeline To actively participate and contribute towards the growth of the organization YOU CAN APPLY IF YOU ARE Passionate about the education sector and content writing B.Tech + M.Tech/MSc (Chemical / Aeronautical / Bio-Technology / Bio-Engineering / Bio-Informatics) SKILLS THAT WE ARE LOOKING FOR Subject matter expertise Proficient in MS office Creative writing Strong conceptual and analytical thinking Effective verbal and written communication Ability to work independently and also in a team

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) About Company: Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers. Join Thermo Fisher Scientific and make a meaningful impact on the world as part of a collaborative team. As a Facility Engineer in the Bioprocess Design Center, you will be responsible for the operation, maintenance, and continuous improvement of our innovative Single-Use Biomanufacturing Facility. Your role will encompass ensuring efficient facility performance, compliance with regulatory standards, and support for biomanufacturing activities. You will collaborate with crossfunctional teams to maintain the facility's infrastructure, utilities, and equipment while driving powerful solutions to improve efficiency and reliability. Responsibilities: Facility Operations and Maintenance Coordinate day-to-day operations of the facility, ensuring all infrastructure and utilities (HVAC, purified water systems, cleanrooms, etc.) meet operational requirements. Perform routine maintenance, inspections, and troubleshooting of facility systems to ensure efficient performance and compliance with industry standards. Support the installation, qualification, and validation of equipment and systems used in single-use biomanufacturing. Develop and implement preventive and predictive maintenance programs to minimize downtime and operational disruptions. Regulatory Compliance and Safety Ensure facility operations adhere to cGMP, OSHA, and other regulatory requirements. Conduct risk assessments and ensure compliance with environmental, health, and safety (EHS) standards. Maintain comprehensive documentation for audits, including maintenance logs, calibration records, and operational procedures. Support the preparation and execution of internal and external inspections and audits. Utility Management Manage critical utilities supporting the bioprocess design center, including steam systems, water purification systems, and air handling units. Monitor utility performance and implement measures to optimize energy efficiency and sustainability. Troubleshoot utility-related issues and coordinate repairs or upgrades with contractors and vendors. Project Management Lead facility improvement projects, including upgrades, expansions, and new system installations, to support evolving biomanufacturing needs. Develop project plans, timelines, and budgets, ensuring completion within scope and schedule. Collaborate with external vendors and contractors to procure and install equipment and materials as needed. Single-Use Technology Support Support the integration and operation of single-use systems within the facility, including bioreactors, filtration systems, and storage solutions. Ensure facility infrastructure is compatible with single-use technologies and flexible for future process changes. Collaborate with process development teams to address facility-related challenges associated with single-use biomanufacturing. Continuous Improvement Identify and implement innovative solutions to improve facility performance, reduce operational costs, and promote sustainability. Stay updated on the latest technologies and standard methodologies in facility engineering and biomanufacturing. Propose and complete projects that improve efficiency and reliability in facility operations. Experience: Bachelor’s or master’s degree in mechanical engineering, Electrical Engineering, Facilities Management, or a related field. 3+ years of experience in facility engineering or operations, preferably in the biopharmaceutical, biotechnology, or healthcare industries. Familiarity with single-use technologies and bioprocessing systems is highly desirable. Experience with cGMP facilities, cleanroom operations, and critical utility management. Strong knowledge of HVAC, purified water systems, cleanroom operations, and facility management systems. Proficiency with CMMS (Computerized Maintenance Management Systems) and facility monitoring tools. Strong analytical and problem-solving skills with a hands-on approach to troubleshooting. Excellent organizational and project management skills with the ability to handle numerous responsibilities. Effective communication and collaboration skills to work with cross-functional teams and external vendors. Certification in facility management (e.g., CFM, PMP) is a plus. Knowledge of automation systems, Building Management Systems (BMS), and environmental monitoring systems. Experience in sustainability initiatives, energy management, and green building practices. Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! At Thermo Fisher Scientific, each one of our +100,000 extraordinary minds have a unique story to tell. ThermoFisher is committed to crafting a diverse work environment that values and respects individuals from all backgrounds. ThermoFisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected

Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (JRF) in a time bound research project for a temporary period, purely on contractual basis in School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India.as per the following details. Position Junior Research Fellow (JRF) Number of Vacancy One Project Title MULTIFUNCTIONAL SILICA COMPOSITE COATINGS ON TI-6AL-4V BY SPIN COATING AND IT’S OPTIMAL IMPLANT/SCAFFOLD FABRICATION FOR BIOMEDICAL APPLICATIONS Sponsoring agency Council of Scientific & Industrial Research (CSIR) CSIR-ASPIRE 01WS(030)/2023-24/EMR-II/ASPIRE Department Department of Chemistry, School of Advanced Sciences (SAS) Project Tenure 3 years Job Description Project aims to develop the usability of defect free coatings and nanofibous scaffolds of bioactive silica glass and it’s composite for biomedical applications. Knowledge about ceramic materials, coatings and corrosion knowledge is required. Strong communication and writing skills are desirable. Essential Qualification Integrated BS-MS/MSc, M.Sc in material science, chemistry, physics, M Tech in nanotechnology or equivalent degree, with 55% marks and with valid NET/GATE test. Upper Age Limit JRF-28Yrs. Age relaxation The upper age limit is relaxable up-to 5 years in the case of candidates belonging to scheduled castes/tribes/OBC, women and physically handicapped candidates. Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m. Principal Investigator Dr. U. Vijayalakshmi Professor (Grade I) Department of Chemistry, School of Advanced Sciences (SAS), Vellore Institute of Technology, Vellore Tamil Nadu – 632014 Send your resume along with relevant documents pertaining to the details of qualifications, GATE/NET score card, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (10/08/2025) through online http://careers.vit.ac.in Please note that the CV should include contact details (address, mobile phone no., email ID), date of birth, qualifications mentioned clearly. Complete information regarding publications of research papers in SCOPUS Indexed Journals should be mentioned in the CV. Incomplete applications will be rejected. No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Job Title: Senior Manager, Scientific Communications Role GCF: L6a Location: Hyderabad, India Company: Amgen About Us: Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Role Description: The Scientific Communications Senior Manager is accountable for planning and delivering innovative scientific and medical content aligned to their designated Therapeutic Area / product (General Medicine, Inflammation, Oncology, Rare Disease, or Obesity), tailored to specific audiences globally via impactful formats and relevant channels. Reporting to a Scientific Communications Therapeutic Area (TA) Lead in India, this leader manages a small team of scientific communication team members and drives the execution of tactical Scientific Communication plans for US and global regions to deliver our Medical and overall product strategies. The Scientific Communications Senior Manager may directly partner with US/Regional Medical planning team and Scientific Communication Operations team members to drive process alignment, standardization, and adoption of innovation and transformational change. This role is responsible for creating and leading high-performing and engaged teams to exceed expectations. Roles & Responsibilities: Develop and deliver high-quality, accurate, and innovative scientific and medical content (DSE/digital/MSL materials/FAQs/Medical Information Letters) tailored to specific audiences in the US and globally via impactful formats and relevant channels. Publication-related deliverables (manuscripts/abstracts/posters/Oral presentations, enhanced content). • Addressing Medical Information inquiries/issues. • Creation of payer-related content, timely support for compendia. Maintain strong partnerships with Scientific Communication Operations team in support of standardization of processes, optimizing systems, and furthering continuous improvement and innovation, including use of digital and multi-channel approaches, as well as definition of impactful KPIs. Drive the execution of a comprehensive scientific communication plan that shifts based on changes in the disease area and treatment landscape and in-depth awareness of insights across local affiliates and cross-functional partners Ensure compliance with relevant Amgen enterprise and Functional SOP(s) and system(s) Assist in recruiting, onboarding, and training of staff members. Support prioritization process, prepare and oversee team assignments to meet program goals on time and within budget. Develop, maintain, cultivate, and influence strong relationships with cross-functional colleagues Foster Amgen culture and motivate high-performing and empowered staff. Basic Qualifications and Experience: Advanced scientific degree: Doctorate degree & 2 years of Global Publication OR Medical Communications OR Medical Value and Access OR Medical Strategy Experience. Master’s degree & 6 years OR Bachelor’s degree & 8 years OR Associates degree & 10 years AND 2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources. Functional Skills: Preferred Qualifications: MD, PharmD, PhD, or DO with 4 or more years of expertise in clinical research, patient care, Clinical Development, Medical/Scientific Affairs, and/or basic research (other doctorate degrees may be considered) Prior experience in Medical/Scientific Affairs or Clinical Development within the biopharmaceutical industry, and/or clinical or research in the therapeutic area An understanding of the pharmaceutical commercialization process and knowledge of the regulatory and legal guidelines affecting promotion of prescription products Experience in publication planning, publications guidelines and transparency standards (e.g., ICMJE, current Good Publication Practice (GPP) Guidelines ) Understanding of Amgen focused disease area and landscape and clinical data to enable critical analysis of scientific literature and communicate implications cross-functionally Demonstrated track record of strategic execution in a matrix environment with limited supervision The ability to work in teams and interface in a dynamic environment across corporate functions Preferred Skills: Knowledge of emerging technologies in medical communications (e.g., AI tools, omnichannel engagement platforms). Strong computer and database skills, particularly with Microsoft Office products Soft Skills: Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to manage multiple priorities successfully Collaborative mindset with a strong sense of accountability and ownership Ability to drive continuous improvement and adapt quickly in a fast-evolving environment Strong project management with ability for self-direction Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Join Amgen's Mission to Serve Patients If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission to serve patients drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together, researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. WHAT YOU WILL DO The Scientific Communications Senior Manager is accountable for planning and delivering innovative scientific and medical content aligned to their designated Therapeutic Area / product (General Medicine, Inflammation, Oncology, Rare Disease, or Obesity), tailored to specific audiences globally via impactful formats and relevant channels. Reporting to a Scientific Communications Therapeutic Area (TA) Lead in India, this leader manages a small team of scientific communication team members and drives the execution of tactical Scientific Communication plans for US and global regions to deliver our Medical and overall product strategies. The Scientific Communications Senior Manager may directly partner with US/Regional Medical planning team and Scientific Communication Operations team members to drive process alignment, standardization, and adoption of innovation and transformational change. This role is responsible for creating and leading high-performing and engaged teams to exceed expectations. Roles and Responsibilities Develop and deliver high-quality, accurate, and innovative scientific and medical content (DSE/digital/MSL materials/FAQs/Medical Information Letters) tailored to specific audiences in the US and globally via impactful formats and relevant channels Publication-related deliverables (manuscripts/abstracts/posters/Oral presentations, enhanced content) Addressing Medical Information inquiries/issues Creation of payer-related content, timely support for compendia Maintain strong partnerships with Scientific Communication Operations team in support of standardization of processes, optimizing systems, and furthering continuous improvement and innovation, including use of digital and multi-channel approaches, as well as definition of impactful KPIs Drive the execution of a comprehensive scientific communication plan that shifts based on changes in the disease area and treatment landscape and in-depth awareness of insights across local affiliates and cross-functional partners Ensure compliance with relevant Amgen enterprise and Functional SOP(s) and system(s) Assist in recruiting, onboarding, and training of staff members Support prioritization process, prepare and oversee team assignments to meet program goals on time and within budget Develop, maintain, cultivate, and influence strong relationships with cross-functional colleagues Foster Amgen culture and motivate high-performing and empowered staff WHAT WE EXPECT OF YOU We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications Doctorate degree with a minimum of 10 years of experience in Global Publication, Medical Communications, Medical Value and Access, or Medical Strategy Master’s degree with a minimum of 12 years of experience Bachelor’s degree with a minimum of 14 years of experience Minimum of 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources Must-Have Skills MD, PharmD, PhD, or DO with 4 or more years of expertise in clinical research, patient care, Clinical Development, Medical/Scientific Affairs, and/or basic research (other doctorate degrees may be considered) Prior experience in Medical/Scientific Affairs or Clinical Development within the biopharmaceutical industry, and/or clinical or research in the therapeutic area An understanding of the pharmaceutical commercialization process and knowledge of the regulatory and legal guidelines affecting promotion of prescription products Experience in publication planning, publications guidelines and transparency standards (e.g., ICMJE, current Good Publication Practice (GPP) Guidelines) Understanding of Amgen focused disease area and landscape and clinical data to enable critical analysis of scientific literature and communicate implications cross-functionally Demonstrated track record of strategic execution in a matrix environment with limited supervision The ability to work in teams and interface in a dynamic environment across corporate functions Preferred Skills Knowledge of emerging technologies in medical communications (e.g., AI tools, omnichannel engagement platforms) Strong computer and database skills, particularly with Microsoft Office products Soft Skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to manage multiple priorities successfully Collaborative mindset with a strong sense of accountability and ownership Ability to drive continuous improvement and adapt quickly in a fast-evolving environment Strong project management with ability for self-direction WHAT YOU CAN EXPECT OF US As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. https://careers.amgen.com EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Sr Associate IS Engineer – Mobility What you will do Let’s do this. Let’s change the world. In this vital role you will be responsible for design, development, delivery, and life cycle of Amgen’s end user technologies. The Mobility team consists of cross-disciplinary IS professionals who understand how to deliver services that span both infrastructure and applications. As a senior member of the Mobility Services team within the Digital Workplace experience (DWX) function, you will play a critical role in defining architecture, enforcing standards, guiding junior engineers, and ensuring secure, scalable, and seamless mobile technology experiences for global end users. You will be working on high visibility projects and play a key role in delivering on IS initiatives and optimizing the end user experience while maintaining the security of Amgen assets and data. You will need to establish and maintain a positive business relationship with users and business partners and will participate in supporting critical mobility services for Amgen. The role will be based out of Amgen India Technology center at Hyderabad Roles & Responsibilities: The MDM Engineer will be responsible for several activities including but not limited to the following: Provide technical leadership and oversight for the global mobile device management ecosystem, including JAMF , Intune , and Apple Business Manager platforms. Define and enforce configuration standards, security baselines, and compliance policies across corporate and shared-use mobile devices. Drive solution design, roadmaps, and project execution for mobile services and applications. Lead validation and risk assessments of new OS and MDM platform updates (iOS, iPadOS, JAMF, Intune), assessing compatibility and security implications. Oversee global L3 support activities, ensuring consistent, high-quality incident resolution and operational stability. Mentor and guide junior engineers, providing configuration reviews, knowledge transfer, and skills development. Collaborate with cross-functional teams (Information Security, Identify & Access Management, Records, Legal) to align services with governance and compliance requirements. Partner with global service owners and vendors to drive improvements in device lifecycle management, user experience, and service KPIs. Lead UAT, pilot programs, and change management for major feature deployments or policy updates. Analyze service trends, conduct root cause investigations, and provide data-driven recommendations using tools like Power BI, Excel, and ServiceNow reporting. Own and maintain SOPs, technical documentation, knowledge bases, and architectural diagrams. Contribute to the development of mobile service strategies, budget planning, and capability assessments. Serve as a key point of escalation and subject matter expert for mobile and endpoint security incidents. Ensures projects are completed on time and within budget Delivers results in an environment consisting of diverse global and matrixed partners including non-dedicated resources Develops relationships with internal business partners, service partners, and vendors to support operational objectives. Ensures risk and compliance by adhering to legal and regulatory guidelines and policies and Standard Operating Procedures What we expect of you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Master's degree / Bachelor's degree and 5 to 9 years of Computer Science, IT or related field experience Preferred Qualifications: 6+ years of technical experience in enterprise mobile endpoint management Solid knowledge of JAMF, Microsoft Intune, Workspace ONE (UEM), Assi and Apple Business Manager Strong knowledge of iOS and iPadOS, including supervised & unsupervised device configurations. Experience managing shared and individual-use mobile devices in corporate settings Strong command of mobile device security principles, MDM configuration frameworks, and application distribution (VPP, Company Portal) Experience leading mobile engineering projects in regulated environments (pharma/healthcare preferred) Prior experience mentoring team members and driving technical decision-making Demonstrated success managing vendor-delivered services in large global environments Proficiency in process automation, scripting (e.g., shell, PowerShell, Python), and integration tools Excellent communication and presentation skills, with ability to interface across technical and non-technical audiences Strong analytical mindset with data interpretation skills using Power BI, Excel, or equivalent tools Proven experience in MS Office Suite & Collaboration tools, including development of advanced Excel spreadsheets, PPT, Teams and SharePoint Excellent problem-solving, team and time management skills Resourceful and proactive in capturing information and sharing ideas Working knowledge of ITIL methodologies and systems including ServiceNow Understanding of Agile methodologies and DevOps Flexibility in supporting global teams Soft Skills: Excellent leadership and team management abilities. Strong communication and interpersonal skills. High level of integrity and ethical standards. Problem-solving and critical thinking capabilities. Ability to influence and motivate change. Adaptability to a dynamic and fast-paced environment. Strong organizational and time management skills. Ability to manage multiple competing priorities in parallel What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. ABOUT THE ROLE Role Description: In this vital role, you will lead the Amgen India, Quality Control Technical Resources Team. This is a unique opportunity to support the global Quality Control network and to learn about the testing of Amgen products through various stages of the product lifecycle. In addition, as this is a newly formed team, the Senior Manager will have the opportunity to develop new business processes and to strategically develop the team structure. The QC Technical Resources team will primarily provide centralized document management support for the global QC Network. This will include the creation and/or revision of controlled documents within Amgen’s enterprise document management system for a variety of QC processes. The Senior Manager Quality Control will provide management oversight of this team while fostering a culture of innovation, quality and collaboration. The Senior Manager will report directly to Amgen India Quality Leadership. This candidate will primarily work during regular working hours (9 AM – 6 PM local time) to enable the business in delivering Amgen’s mission to serve patients and may lead a shift-based team that provides coverage in support of the Amgen network across multiple time zones. The candidate may need to work outside of his/her routine workday to support business needs and will be responsible for determining the same for their staff. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN). The candidate will also lead the remote support from AIN to Amgen sites across multiple time zones globally. Roles & Responsibilities: The Senior Manager Quality Control will be accountable for the following activities: Daily management of the Quality Control Technical Resources team Responsible for organizing team resources to ensure that agreed upon due dates are met for QC Network requests Responsible for creating and maintaining business processes and tools that will facilitate the management and visibility of QC network requests Responsible for ensuring that the Technical Resources team has access to the required laboratory information management and enterprise systems needed to carry out document management tasks (for example, LIMS, electronic laboratory notebook). Responsible for leading issue resolution and problem-solving exercises within the team and cross-functionally, as needed Support staff training, career development and performance management Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements. Additional Responsibilities: Participate in Amgen global network teams Establish and enable LEAN principles across area of responsibility Establish and enable department goals, strategies and KPIs Champion site and QC global process improvements Interfaces with management on significant matters, often requiring the coordination of activity across organizational units Plans and organizes project assignments of substantial variety and complexity Translates complex data into actionable information and applies strong technical knowledge to meet business objectives Identifies process gaps, introduces innovative solutions, and leads operational excellence projects to improve efficiency and productivity, while decreasing expense/operating costs. Leads root cause analysis discussions for more complex problems to develop and efficiently implement effective permanent solutions. Basic Qualifications and Experience: Master’s degree with 12-16 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience AND 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources Functional Skills: Must-Have Skills: Experience working and leading teams in a cGMP laboratory environment. Strong technical writing skills within a highly regulated environment. Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control. Experience managing staff and/or leading teams, projects, programs or directing the allocation of resources. Good-to-Have Skills: Track record of building or participating as a member of high performing team. Experience with various laboratory computer systems and applications. Strong leadership and negotiation skills with a demonstrated ability to influence different styles. Demonstrated innovative thinking and ability to transform work organizations. Exposure to Operational Excellence initiatives. Understanding of quality management systems and quality control processes related to drug substance and drug product for clinical and commercial operations. Demonstrated ability to navigate through ambiguity and provide structured problem solving. Demonstrated ability to coordinate multi-functional project teams and deliver on schedule. Demonstrated ability to coordinate and lead cross-functional teams. Demonstrated ability to find opportunities and implement new technologies and services to transform the business into a more agile, efficient and effective organization. Demonstrated skills in staff motivation, coaching/mentoring and professional development. Great teammate who can collaborate and provide leadership through influence to achieve the required results. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Join Amgen's Mission to Serve Patients If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission to serve patients drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together, researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. WHAT YOU WILL DO In this vital role, you will be a key part of the R&D Finance team, supporting Amgen’s Research & Development function and reporting to the Amgen India R&D Finance lead. You will: Manage preparation of budgets, forecasts, and Long-Range Scenarios Provide consultancy and financial decision support analysis to various R&D functions and departments Interact with a wide range of staff across Amgen Roles and Responsibilities Planning Manage quarterly budget and planning activities including headcount, operating expenses, and capital expenses Prepare monthly and quarterly headcount and operating expenses reports for business functions Communicate and provide direction to function heads about financial trends and their business implications Master Data Maintenance Manage and update financial master data across all systems to ensure accuracy and integrity Handle cost center creation, modification, and deactivation aligned with the organizational structure Create Work Breakdown Structures (WBS) for precise project tracking and financial reporting Accounting Manage month-end close processes, including monthly and quarterly analysis Oversee monthly and quarterly Prepaids and Accruals processes Productivity Implement and track productivity metrics to support management reporting Partner with the business to drive efficiency Projects Provide business analysis and decision-making support, including financial analyses and modeling of “what if” scenarios Lead continuous improvement projects using digital technologies and automation Perform any other ad hoc duties as required WHAT WE EXPECT OF YOU We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications Master’s degree with 8 to 10 years of experience in accounting, finance, or business administration in a similar position in an international environment OR Bachelor’s degree with 10 to 12 years of similar experience Must-Have Skills Experience in Budgeting, Forecasting, and HC Planning Biotechnology or Pharmaceutical experience preferred Strong organizational and time-management skills with the ability to manage several priorities Exceptional attention to detail and accuracy in all deliverables Ability to work independently and proactively in a fast-paced environment High proficiency with Microsoft Office Suite (Excel, PowerPoint, Power BI), Hyperion, SAP, Anaplan, and virtual collaboration tools (e.g., Teams) Preferred Skills Experience working in a multinational environment with global teams Familiarity with project management tools and methodologies Strong business acumen, critical thinking, and execution excellence Soft Skills Excellent verbal and written communication skills High degree of professionalism and interpersonal skills Strong problem-solving abilities and adaptability to changing priorities Collaborative mentality and ability to build positive relationships across diverse teams Resilience, discretion, and the ability to thrive under pressure WHAT YOU CAN EXPECT OF US As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. https://careers.amgen.com EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller, and longer. We discover, develop, manufacture, and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what is known today. Manager Information Systems – FinOps Analyst What you will do As a Manager Information Systems - FinOps Analyst at Amgen, you will provide data‑driven cost control for Amgen’s enterprise Veeva Vault estate. You will own license utilization analytics, track cloud spending, prepare KPI packs for vendor QBRs, and partner with Engagement Managers to optimize seat allocation, service credits. Your insight will enable the business to scale Veeva adoption while keeping total cost of ownership in check and ensuring compliance with contractual terms. Roles & Responsibilities: License & Utilization Analytics – pull usage feeds from Vault Admin reports; build Power BI dashboards showing active‑seat ratios, sandbox trends, environment counts. Forecast & True ‑up Support – model license forecasts, highlighting surplus or shortage by domain; provide data packs for annual true‑up negotiations. SLA & KPI Reporting – compile monthly service‑level scorecards (uptime, incident MTTR, release success‑rate) for Vendor & Governance Lead; feed metrics into QBR decks. Cost Optimization Initiatives – identify dormant accounts, over‑provisioned environments, or underused modules; recommend reclamation or re‑allocation actions to save 5‑10 % annually. Contract Compliance Tracking – monitor contract clauses (seat caps, sandbox limits, disaster‑recovery charges); flag variances and support remediation plans. Budget management – support Veeva Platform leadership with planning, tracking and updating yearly product and service budgets following Amgen’s Finance processes. Work closely with functional Finance Analysts and central Technology portfolio teams. Budget vs Actuals Reconciliation – work with Finance to reconcile platform invoices, accruals, and charge‑backs to functional cost centers. Stakeholder Engagement – partner with Client‑Engagement management and Product Owners to explain cost drivers, provide on‑demand license views, and capture upcoming demand signals. Shift Information : This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required based on business requirements. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications. Basic Qualifications: Doctorate degree / Master's degree / Bachelor's degree and 8 to 13 years in IT financial analysis, cloud/SaaS cost management, or software asset management Must-Have Skills: Proven experience building license‑ and usage‑dashboards (Excel Power Query, Power BI, or Tableau). Solid grasp of SaaS pricing and true‑up mechanisms; can translate contract terms into measurable metrics. Strong analytical and data‑storytelling ability – comfortable turning raw usage logs into executive‑ready insights. Working knowledge of ITIL SLA metrics (uptime, MTTR) and KPI reporting. Excellent Excel / SQL skills for data wrangling and reconciliation. Good-to-Have Skills: Familiarity with Veeva Vault admin reports or comparable SaaS admin tooling (Salesforce, ServiceNow). Exposure to FinOps or Software Asset Management frameworks (e.g., FinOps Foundation, ISO 19770). Experience with procurement or vendor‑management processes (RFx, contract renewals). Good understanding of GxP / SOX considerations for validated SaaS spending. Soft Skills: Detail‑oriented and deadline‑driven; spots anomalies before they become issues. Confident communicator – able to explain cost drivers to both finance and technical audiences. Collaborative mindset; partners easily with Vendor Managers, Product Owners, and Finance analysts. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Join Amgen's Mission to Serve Patients You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. What you will do Let’s do this. Let’s change the world. In this vital role you will provide operational management of Amgen’s India HR Connect team and will be responsible for the continued modernization and transformation of India HR service delivery with a focus on elevating the employee experience. The Manager will use technology solutions (ServiceNow and Workday) to drive self-service, speed of resolution, and reduce ticket volume while enhancing the employee life cycle overall experience. This role involves managing the day-to-day operations of the India HR Connect team, overseeing staff inquiries, managing HR processes, and driving improvements in HR service delivery. The HR Connect Manager will work closely with various HR functions in India to ensure alignment and effective communication. Roles and Responsibilities: Lead the service delivery team with various levels of inquiries via multichannel options including transactions through Workday and inquiries through ServiceNow. Participate in and/or lead and/or coordinate (system/process improvement) projects / audits Ensure that HR inquiries and transactions are processed according to global processes within service level agreements and act as point of contact for HR Connect with complex inquiries Act as a coach for HR Connect team member(s) and support on best practices, solutions and approaches Support the HR service center & HR COE’s with Business SME support related to the ServiceNow module and Workday Support specialists in working with HR Tech Team on HR system improvements and translate business needs into technical requirements Act as a liaison between India HR Connect, India HR Knowledge Experts, India HR Technology, and India local HR to translate business needs into technical solutions. Lead/Coordinate/Participate in system and process improvement projects related to Workday, Service Now and HR processes. Set goals, coach others, and encourage team members to take ownership of their personal development. Encourage and develop solid knowledge sharing concepts within the team for better cross collaboration. Partner with Knowledge Management team to ensure accuracy and comprehensiveness of the content in the team’s knowledge base program and the MyHR portal (tier 0). Facilitate knowledge sharing and train the HR Connect team on HR practices and system processes to be designated as subject matter experts. Sponsor and actively contribute to support of quality customer service initiatives across the globe. Evaluate workforce needs, and resource allocation needs to support existing and additional expansion scope of work. Sponsor change management and other transformational efforts to increase service excellence. Manage highly confidential information of staff at all levels within the organization. Deliver metrics, measurements and data insights to internal and external team members in India to inform conclusions and support decision-making. Develop engaging relationships with stakeholders through trust and teamwork. Partner with local HR teams to share standard practices and promote consistency and cohesiveness with compliance and regulation in mind. Partner with various business areas and IT to evaluate how best to use ServiceNow technology to meet evolving business requirements and deliver the best digital employee experience in India. Lead other projects / activities as requested and participates in other cross-functional projects in representation of the HR Staff Services team. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The Human Resources professional we seek is a leader with these qualifications: Basic Qualifications: Master’s degree and 9 to 12 years of Human Resources experience Preferred Qualifications: Must-Have Previous experience in team management and leadership Solid understanding of HR processes and best practices Strong working knowledge of Workday Extensive working knowledge of ServiceNow Good-to-Have Experience working in a multinational organization Soft Skills: Excellent communication and interpersonal skills Ability to handle sensitive and confidential information with discretion Strong problem-solving and analytical skills What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Associate QC – QC Systems Templating Role Name: Associate QC Department Name: Quality Control Role GCF: 3 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. ABOUT THE ROLE Role Description: Let’s change the world. Amgen is hiring for an Associate to support the Electronic Lab Notebook (ELN) and consumable inventory system infrastructure in the Quality Control (QC) network. This candidate will primarily work a shift-based schedule to enable the business in delivering Amgen’s mission to serve patients. The candidate may need to work outside of his/her routine workday to support business needs. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN) and provide remote support from AIN to Amgen sites across multiple time zones globally. Roles & Responsibilities: This position will be responsible for the creation, revision and qualification of templates for analytical method executions in ELN. Creation and revision of consumable templates will also be in the scope of responsibility. The Associate will ensure assigned tasks are carried out according to the correct procedures, best practices, and service level agreements for QC standardization. Coordination with members within the team at AIN on the same shift and members of the team at AIN on different shifts will be critical in ensuring deliverables are met in accordance with schedule. To effectively provide support, candidates must demonstrate proficiency in virtual communication tools and have experience interacting in remote collaborations. The following are some examples of tasks for the position Creation and revision of ELN templates Qualification of ELN templates Creation and revision of consumable templates Understand and follow established instructions to complete assigned deliverables within expectations Collaboration with AIN team members to support the QC network needs Ensuring training is up to date Additional responsibilities may involve: Assistance in providing performance metrics Basic Qualifications and Experience: Master’s degree with 1-3 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience. Functional Skills: QC lab testing experience Exposure to ELN applications Microsoft Office proficiency Familiarity with Good Manufacturing Practices and Good Documentation Practices Soft Skills: Excellent English verbal and written communication skills Ability to learn quickly with attention to detail Delivering results right first time within a team environment EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Khammam, Mahbubnagar, Nizamabad, Warangal Link Copied RSS Feed Job Title: Pharma Sale Executive Department: Sales & Customer Support Location: Warangal , Mahbubnagar, Nizamabad,Khammam Employment Type: Full-Time Job Summary: We are looking for a proactive and knowledgeable Customer Service Representative (CSR) to support our surgical product division. The role involves engaging with doctors, OT staff, and distributors to deliver product education, support during surgeries, and customer service excellence. ThePSE will contribute to sales growth and build strong customer relationships by ensuring high levels of product knowledge, responsiveness, and professionalism. Key Responsibilities Communicate product features and clinical applications accurately to existing and prospective customers. Build and maintain strong, long-term customer relationships to increase satisfaction, trust, and brand loyalty. Identify customer needs and convert opportunities into successful sales to meet or exceed territory targets. Collect and report field-level data (market feedback, customer insights, competitor activity) to management. Assist in market development initiatives and support brand visibility in the assigned territory. Attend surgical procedures and provide on-site support and product consultation. Ensure effective coordination with distributors for product availability, timely delivery, and stock management. Adhere to company values, compliance standards, and systems at all times. Educational Qualifications: Minimum: Graduate in Science, Pharmacy, Biotechnology, or Life Sciences Candidates from non-science backgrounds will be considered only with relevant experience in healthcare Experience Required: 23 years of post-graduation experience in sales, marketing, or customer service Prior experience in the healthcare, surgical, or medical device industry is strongly preferred Mandatory Skills: Self-motivated and result-oriented Excellent communication and interpersonal skills Core selling and negotiation skills Strong customer relationship management abilities Desired Skills: Basic knowledge of internet and MS Office tools Willingness to work in Operating Theatre (OT) environments Exposure to healthcare workflows and hospital systems Eagerness to learn the clinical and surgical applications of medical products Other Requirements: Willingness to travel across the assigned territory Flexible with working hours based on customer or surgical needs Professional appearance and conduct Experience 1 - 4 Years Salary 3 Lac 50 Thousand To 4 Lac P.A. Industry Sales & Marketing / Business Development / Telecaller Qualification B.Pharma, B.Sc Key Skills Self-motivated and Result-oriented Excellent Communication and Interpersonal Skills Core Selling Negotiation Skills Strong Customer Relationship Management Abilities Pharma Sales

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do Let’s do this. Let’s change the world. In this vital role you will join a collaborative team implementing and supporting the next generation of safety platforms and supporting technologies. In this role, you will analyze and resolve issues with adverse event data and file transmissions across integrated systems, leveraging data analytics to identify trends, optimize workflows, and prevent future incidents. Collaborating closely with various teams, you will develop insights and implement solutions to improve system performance, ensuring reliable and efficient data flow critical to safety operations. Monitor, solve, and resolve issues related to adverse event data processing across the safety ecosystem. Triage and conduct detailed investigations into system disruptions, data anomalies, or processing delays to determine and nature and scope of the problem Work closely with internal teams, external vendors, and business partners to address dependencies and resolve bottlenecks for critical issues and triage the issues and provide L1/L2 support Identify inefficiencies and propose data-driven solutions to optimize and enhance reliability. Present findings and recommendations to leadership, ensuring data-driven decision-making and clear transparency into system operations. Support compliance with Key Control Indicators (KCI) and chips in to overall process governance What we expect of you We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications. Basic Qualifications: Bachelor’s degree and 2 to 6 years of Life Science/Biotechnology/Pharmacology/Information Systems experience Demonstrated expertise in monitoring, troubleshooting, and resolving data and system issues. Good understanding of Pharmacovigilance process and knowledge on safety systems like (Argus, Arisg, LSMV etc.) Basic familiarity with ITSM tools like Service now or JIRA Identify and escalate potential safety/compliance issues. Familiarity with database technologies and querying tools, including SQL (Oracle SQL, PL/SQL preferred). Experience with testing methodologies, tools, and automation practices. Familiarity with regulatory compliance testing (e.g., FDA 21 CFR Part 11, GAMP Experienced in Agile methodology Preferred Qualifications: Understanding of API integrations and middleware platforms (e.g., MuleSoft). Outstanding written and verbal communication skills, and ability to explain technical concepts to non-technical clients Sharp learning agility, problem solving and analytical thinking Experienced in GxP systems and implementing GxP projects Experience in SDLC, including requirements, design, testing, data analysis, change control Certification: SAFe for Teams certification (preferred) Soft Skills: Excellent analytical and troubleshooting skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to manage multiple priorities successfully Team-oriented, with a focus on achieving team goals Ability to deal with ambiguity and think on their feet Shift Information: This position requires you to work a later shift and will be assigned third shift schedule (Overnight shift on a rotational basis). Candidates must be willing and able to work during evening or night shifts, as required based on business requirements. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this important role. The Financial Insights & Technology (FIT) team was created to: (1) maintain and build upon work/improvements enabled by various initiatives, (2) implement standardized reporting capabilities, (3) implement and maintain policies, processes and systems needed to drive an efficient and effective reporting environment and (4) explore new ways to evolve reporting, in the spirit of continuous improvement, to improve financial insights across the global finance organization. The Associate will be part of the FIT (Financial Insights & Technology) Data Analytics & Processes team within Corporate Finance. This role will be based in India – Hyderabad. What will you do In this vital role as an Associate Data Analytics, you will play a meaningful role in Financial Data Integrations and Analysis for the global Amgen organization. Key responsibilities include but are not limited to: Developing a strong understanding of Amgen’s financial data and systems to support reporting, integration, and data request needs across initiatives. Working in close partnership with client-facing members of the FIT Reporting & Analytics (FITRA) team to design, develop and augment the financial datasets Owning and managing daily operational data processes in Databricks, ensuring they run reliably and efficiently. Creating and maintaining data pipelines in Databricks & Prophecy and building Tableau/Power BI dashboards to enable enterprise reporting and support future analytics needs. Writing SQL queries and creating ad-hoc reports based on end-user or team requests. Participating in project work to support financial dataset requests for other functions or groups within Amgen Identifying opportunities for automation and process improvement to streamline and enhance performance of data pipelines. Validating datasets through Databricks and Tableau dashboards Maintaining FITDAP documentation and code base. Involvement in the Financial Data Product Team, as well as supporting other initiatives. Key elements to success in this role include understanding Amgen’s financial systems and data, understanding how to design datasets compatible with Tableau/Power BI reporting requirements, understanding how to take “business requirements” from colleagues and customers to translate them into dataset design. What we expect of you We are all different, yet we all use our outstanding contributions to serve patients. The Associate Data Analytics professional we seek is a go-getter with these qualifications. Basic Qualifications Master’s degree OR Bachelor’s degree and 2 years of Finance or Information Systems experience OR Associate degree and 6 years of Finance or Information Systems experience Or High school diploma / GED and 8 years of Finance or Information Systems experience Preferred Qualifications Experience with financial statements and Amgen Finance experience is a plus Experience with data analysis and data visualization solutions such as Tableau, Power BI, Databricks, Prophecy, and Alteryx Designer Basic understanding of building ETL pipelines using data integration tools such as Prophecy, Alteryx, Databricks or similar platforms Familiar with Hyperion Planning, SAP, and scripting languages like SQL or Python. Well-versed in MS Suite, especially MS Excel (for data handling tasks such as pivot tables, VLOOKUP, data analysis tools, formatting) and proficient in MS Word and MS PowerPoint Excellent analytical and problem-solving skills. Able to work under a minimum supervision while being diligent with remote work and remote collaboration Strong communication and presentation skills Able to work in matrixed teams, across geographic and functional reporting lines

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF Funded Project in the Department of Physics, School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “Development of cost-efficient and scalable perovskite based colloidal nanoparticles for high performance plastic scintillators” Qualification : M.Sc./ M.Tech. in Physics/ Materials Science or related fields from recognized universities/institutes with a minimum of first class and with GATE / CSIR-UGC JRF / NET-LS qualification. Mandatory Skills : Candidates should have a strong research background in synthesis and characterization of nanomaterials. Experience with colloidal semiconductor nanomaterials and related photo physics is desirable. Stipend : Rs. 37,000 p.m. + 8% HRA for the first two years (JRF); Rs. 42,000 p.m.+ 8% HRA for the third year (SRF) will be as per Institute norms. No. of Vacancies : 01 Post (ONE) Age Limit (if any) : Not exceeding 30 years i.e. Age must be from 18 to 30 years Sponsoring Agency : ANRF, PMECRG program, New Delhi, India Duration : 36 Months Principal Investigator : Dr. Abhinav Anand, Assi stant Professor, Department of Physics School of Advanced Sciences, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Interested candidates with the above-mentioned qualifications can send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before ( 18/08/2025) through the website: http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Why join Stryker? Looking for a place that values your unique talents? Discover Stryker's award-winning culture. We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific. Job description We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific. Who we want: Dedicated achievers . People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in function Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to simplify, standardize and automate Effective communicators . People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders, senior management, and their teams. Self-directed imitators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes. What you will do Independently processing results of PFA assessments. Initiate, organize and coordinate global containment actions Ensure that data is documented for the different sites. Together with the PFA specialist create a communication to affected parties. Provide necessary information to regulatory compliance team for reporting. Presenting PFA/commercial hold relevant processes and cases during audits Preparing weekly, monthly and quarterly Commercial Hold relevant statistics Performing training of colleagues and managers by procedural changes What you need B. Tech / M.Tech Mechanical, Biotechnology with hands on experience of working on PFAs, and Commercial Holds. Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability. Poses the ability to lead colleagues in other departments to perform the necessary actions for a timely Containment action Hands on experience of Risk Management process as per ISO 14971 Demonstrated ability to work effectively with various work groups to assure conformance to regulatory requirements, internal processes, and policies. Demonstrated ability to self-motivate, ability to prioritize tasks in a deadline-driven environment. Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams. Sound knowledge on complaint handling process of medical devices will be an added advantage Applied understanding of GDP, ISO 9001 & ISO 13485 (Good to have). Good understanding of FDA 21CFR Part 822 / 820 (Good to have) Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Job Opening: Lab Assistants – Multiple Departments (Non-Teaching) Institution: SIMATS Engineering, Saveetha Institute of Medical and Technical Sciences Location: Thandalam Campus, Chennai – 602 105 Job Type: Full-Time Salary: Attractive pay for the right candidate SIMATS Engineering is hiring Lab Assistants for the following departments: Computer Science and Engineering (CSE) Electronics and Communication Engineering (ECE) Electrical and Electronics Engineering (EEE) Physics Chemistry Biomedical Engineering Bioinformatics Biotechnology Eligibility Criteria: Qualifications: Diploma B.E. / B.Tech B.Sc. / M.Sc. (Physics, Chemistry, Biotechnology, etc.) Freshers and experienced candidates with relevant technical skills are welcome to apply. How to Apply: Send Resume to: recruitment.sse@saveetha.com Apply Online: https://forms.gle/BwXQxiBjq2p4kv248 College Website: https://simatsengineering.com/ Postal Address: SIMATS Engineering Saveetha Institute of Medical and Technical Sciences Saveetha Nagar, Thandalam Campus Chennai – 602 105 Job Types: Full-time, Permanent Pay: From ₹18,000.00 per month Work Location: In person

Domain: Animal Cell Culture | Molecular Biology | CRISPR | Transgenic Models We are hiring a Research Assistant with 1–3 years of hands-on experience in: Animal cell culture Molecular biology techniques (PCR, Western blot, qRT-PCR, etc.) CRISPR gene editing Transgenic model development (preferably zebrafish or rodent models) Key Responsibilities: Execute experiments in cell and molecular biology Maintain and culture various animal cell lines Perform gene editing and assist in the generation/maintenance of transgenic models Maintain detailed experimental records and generate reports Support ongoing research and development projects Coordinate with cross-functional teams for data interpretation and documentation ✅ Qualifications & Skills Master’s degree in Biotechnology, Molecular Biology, Cell Biology, Genetics , or related fields 1–3 years of laboratory experience in research or CRO setups Strong foundation in molecular cloning, RNA/DNA isolation, cell line maintenance, and transfection Practical exposure to CRISPR/Cas9 gene editing tools (design, delivery, validation) Experience with zebrafish or rodent models (preferred but not mandatory) Strong documentation, communication, and teamwork skills 📩 Apply Now Interested candidates can send their CV to reachwbr@gmail.com For queries, contact us at 📞 7904195106 .

Job Title: Senior Technologist – Reproductive Biology & Animal Genomics Locations: Office/Research HQ: Ahmedabad, Gujarat Plant site: Modasa, Aravalli district, Gujarat Qualifications: B.E./B.Sc./M.Sc. in Biotechnology OR MVSc in Animal Reproduction (gynecology / embryo transfer) or Animal Genomics Minimum 10 years’ experience in cattle breeding, embryo transfer, dairy farm R&D, or animal genomics Key Responsibilities: Lead embryo transfer programs for cattle, coordinate OPU-IVF workflow Manage selection, breeding strategies and genetic improvement plans Oversee implementation of genomics tools (e.g. SNP, genomic selection data) Mentor/district-level technical teams at the dairy farm and plant Liaise between plant operations (Modasa) and research HQ (Ahmedabad) Ensure quality control, SOP adherence (animal welfare, biosecurity) Conduct data analysis, generate reports, support audits or FSSAI compliance Collaborate with R&D on genetic enhancement, productivity optimization Skills & Competencies: Hands‑on experience with embryo transfer (ET), IVF protocols Knowledge of cattle reproductology and farm practices Familiarity with genomic technologies and statistical analysis Strong documentation and coordination skills Excellent communication in English, Gujarati and/or Hindi for both locations Work Setup: Split between Ahmedabad (HQ / research office) and Modasa farm/plant Regular travel and periodic on-site supervision Job Type: Full-time Pay: ₹960,000.00 - ₹1,140,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: cattle breeding, embryo transfer,R&D, or animal genomics: 10 years (Required) Work Location: In person

Total no. of Post: Project Associate – I (1 number) Walk-in Interview on 04.08.2025 at CSIR-CSMCRI-Marine Algal Research Station, Mandapam camp-623519 Applications are invited from the talented and motivated candidates for working in the following project. Project title: “Process development for tank-based cultivation technology for edible green seaweed Ulva towards functional food application”, funded by ANRF under IRG (formerly SERB-EMEQ), New Delhi. P.C. No.: GAP-2181 Name of the Post Project Associate-I (1 number) Nature of Work Cultivation of edible seaweed Ulva , tank cultivation of Ulva Essential Qualification M.Sc., in Marine Science / Botany / Biotechnology / Biochemistry / Life Sciences Desirable Qualification Experience on Ulva / edible seaweed / seaweed cultivation in tanks Monthly emolument (a) Rs. 31000/- + HRA for those candidates who have qualified CSIR/UGC/ICAR/ICMR NET incl. lectureship / Assistant Professorship or GATE OR those who qualified National level examinations conducted by Central Government Departments like DBT/DST or equivalent and/or their Agencies and Institutions. (b) Rs. 25000/- + HRA for others who do not fall under (a) above. Age limit 35 years (Relaxation in age as per CSIR norms) Duration: These positions are purely temporary and co-terminus with the project. It would, not confer any right/claim implicit or explicit for any candidate for claiming absorption in CSIR- CSMCRI. The engagement of a project staff in different projects either in the CSIR - Central Salt & Marine Chemicals Research Institute, Bhavnagar or different Laboratories/Institutes of CSIR taken together shall not exceed 06 years in any case. It would, therefore, not confer any right/claim implicit or explicit for any candidate for claiming extension or absorption in CSIR-CSMCRI, Bhavnagar. Interview Details: Interested candidates should appear before the Selection Committee for an interview test at CSIR-CSMCRI-Marine Algal Research Station, Mandapam camp-623519, Tamil Nadu on 04 th August 2025, Monday at 09.30 AM in the institute. Required Documents: Please bring an application with full particulars, including: Full name and postal address with email and phone number (application form attached), Date of birth and recent photograph. Educational qualifications and experience (if any) with photocopies of certificates/testimonials. Also, bring the following original documents (compulsory): Certificates and mark sheets (Degree/Diploma, etc.) of educational qualifications and proof of date of birth mentioned in the application (degree certificate is compulsory). GATE/NET Score Card, validity of the score, and details of seminars/projects done in the Master’s course. Experience certificates and testimonials. "No Objection Certificate" from the present employer if employed in a Government/Semi-Government or Autonomous Organization. For queries, please email dineshks@csmcri.res.in. No TA/DA will be provided for attending the interview.

Company Description AURA Biotechnologies, based in Chennai, specializes in innovative technologies to expedite pharmaceutical and biotechnology R&D processes while reducing development costs. The company operates an integrated manufacturing facility at SIPCOT Industrial Complex in Manamadurai, Tamil Nadu, and is ISO 9001:2008 certified. AURA Biotech excels in biopharmaceutical and agro chemicals development, including recombinant and non-recombinant therapeutic proteins, and offers assay services, biosimilar development, and analytical research adhering to EMEA and FDA guidelines. Additionally, they extract biopolymer products from natural sources and engage in various business models such as technology development, process optimization, and custom assay development. Role Description This is a full-time, on-site role for a Regional Key Account Manager, located in Chennai. The Regional Key Account Manager will be responsible for managing and nurturing relationships with key accounts, developing comprehensive business plans, and providing exceptional customer service to meet client needs. The role involves analyzing business metrics, creating strategic plans to drive growth, and coordinating with internal teams to ensure customer satisfaction and account success. Qualifications Strong Account Management and Key Accounts skills Exceptional Customer Service abilities Proficiency in Business Planning and developing strategic growth plans Excellent Analytical Skills to interpret business metrics Bachelor's/Master's degree in Biotechnology Excellent communication and interpersonal skills Ability to work independently and in a team environment Experience in the pharmaceutical, agriculture or biotechnology industry is must

Job Description Field Manager, Technical This role is responsible for providing technical support to the concerned Zonal Sales team, by conducting technical training related to animal health and products to AFMs, organizing and participating in the technical seminars/ meetings for Animal Health practitioners and dairy Farmers in coordination with the Sales team for sharing technical information and attending customer complaints. Primary Responsibilities Include, But Are Not Limited To Providing Technical Services to internal team and external customers in assigned geography including on-site customer visits & off-side telephonic support as well. Executing a comprehensive technical service plan for maximizing Organizational goals. Group customer meetings to create awareness about relevant scientific practices and advancements with the objective of becoming a partner of choice among customers. Technical upgradation of the internal sales team in assigned geography Staying ahead of the curve for recent technical developments in the Ruminant Industry and preparing internal competencies to provide customer support. Supervising local clinical trials and market support studies under the guidance of the national technical manager. Supervise and provide timely and effective technical materials that maximize selling efforts. Techno-commercial view while discussing with customers. Collaboration with relevant Technical & Veterinary Education institutes in assigned geographies to further improve our image as Science Driven Organization Any other assigned task which can help in improving business. Qualifications Degree in Veterinary Sciences B.V.Sc. & A.H. (M.V.Sc. will be preferred) 2-3 years of field experience to handle all field situations and provide technical solutions to customer needs. Skills & Competencies English communication, technical training and presentation, Knowledge of animal health & diseases, Veterinary Gynecology, Medicine, Pharmacology, Animal Health Management, and Pharma product experience is highly essential. An individual has the confidence to handle adverse situations in the field.Role Specific To provide technical support to the sales and marketing team and meet their training needs and handle customer technical complaints. opportunity employer, committed to fostering an inclusive and diverse workplace. Our Animal Health Division is a trusted global leader in veterinary medicine, dedicated to preserving and improving health, well-being, and performance of animals and the people who care for them. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society, and our planet. Through our commitment to The Science of Healthier Animals®, we offer veterinarians, farmers, pet owners and governments one of the widest ranges of veterinary pharmaceuticals, vaccines and health management solutions and services as well as an extensive suite of digitally connected identification, traceability and monitoring products. We invest in dynamic and comprehensive R&D resources and a modern, global supply chain. We are present in more than 50 countries, while our products are available in some 150 markets. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation Domestic VISA Sponsorship Travel Requirements 75% Flexible Work Arrangements Not Applicable Shift Valid Driving License Hazardous Material(s) Required Skills Preferred Skills Accountability, Accountability, Animal Biotechnology, Animal Health Care, Animal Husbandry, Animal Physiology, Animal Science, Client Facing, Client Management, Clinical Trial Designs, Clinical Trials, Collaboration Tools, Communication, Competency Mapping, Cow Milking, Customer Engagement, Customer Marketing, Customer Satisfaction, Customer Service, Customer Service Management, Dairy Science, Document Management, Field Auditing, Field Marketing, Field Research {+ 23 more} Job Posting End Date 07/31/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R293230

Who we want: Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in function Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to simplify, standardize and automate Effective communicators. People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders, senior management, and their teams. Self-directed imitators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes. What You Will Do Independently processing results of PFA assessments. Initiate, organize and coordinate global containment actions Ensure that data is documented for the different sites. Together with the PFA specialist create a communication to affected parties. Provide necessary information to regulatory compliance team for reporting. Presenting PFA/commercial hold relevant processes and cases during audits Preparing weekly, monthly and quarterly Commercial Hold relevant statistics Performing training of colleagues and managers by procedural changes What You Need B. Tech / M.Tech Mechanical, Biotechnology with hands on experience of working on PFAs, and Commercial Holds. Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability. Poses the ability to lead colleagues in other departments to perform the necessary actions for a timely Containment action Hands on experience of Risk Management process as per ISO 14971 Demonstrated ability to work effectively with various work groups to assure conformance to regulatory requirements, internal processes, and policies. Demonstrated ability to self-motivate, ability to prioritize tasks in a deadline-driven environment. Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams. Sound knowledge on complaint handling process of medical devices will be an added advantage Applied understanding of GDP, ISO 9001 & ISO 13485 (Good to have). Good understanding of FDA 21CFR Part 822 / 820 (Good to have) Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Job Title: Senior Technologist – Reproductive Biology & Animal Genomics Locations: Office/Research HQ: Ahmedabad, Gujarat Plant site: Modasa, Aravalli district, Gujarat Qualifications: B.E./B.Sc./M.Sc. in Biotechnology OR MVSc in Animal Reproduction (gynecology / embryo transfer) or Animal Genomics Minimum 10 years’ experience in cattle breeding, embryo transfer, dairy farm R&D, or animal genomics Key Responsibilities: Lead embryo transfer programs for cattle, coordinate OPU-IVF workflow Manage selection, breeding strategies and genetic improvement plans Oversee implementation of genomics tools (e.g. SNP, genomic selection data) Mentor/district-level technical teams at the dairy farm and plant Liaise between plant operations (Modasa) and research HQ (Ahmedabad) Ensure quality control, SOP adherence (animal welfare, biosecurity) Conduct data analysis, generate reports, support audits or FSSAI compliance Collaborate with R&D on genetic enhancement, productivity optimization Skills & Competencies: Hands‑on experience with embryo transfer (ET), IVF protocols Knowledge of cattle reproductology and farm practices Familiarity with genomic technologies and statistical analysis Strong documentation and coordination skills Excellent communication in English, Gujarati and/or Hindi for both locations Work Setup: Split between Ahmedabad (HQ / research office) and Modasa farm/plant Regular travel and periodic on-site supervision Job Type: Full-time Pay: ₹960,000.00 - ₹1,140,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: cattle breeding, embryo transfer,R&D, or animal genomics: 10 years (Required) Work Location: In person