3723 Biotechnology Jobs - Page 48

Mumbai location. Remote setup** ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Position Overview The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. Responsibilities Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH-GCP guidelines Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely Provides regular site status information to team members, trial management, and updates trial management tools Completes monitoring activity documents as required by PRA SOPs or other contractual obligations Works closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues Escalates site and trial related issues per SOPs, until identified issues are resolved or closed Performs essential document site file reconciliation Performs source document verification and query resolution Assesses IP accountability, dispensation, and compliance at the investigative sites Verifies Serious Adverse Event (SAE) reporting according to trial specifications and ICH-GCP guidelines Communicates with investigative sites Updates applicable tracking systems Ensures all required training is completed and documented Serves as observation visit leader Facilitates audit s and audit resolution Mentors junior level CRAs and serves as a resource for new employees Serves as observation and performance visit leader May be assigned additional Clinical Operations tasks May serve as a resource for and interact with other functional areas to resolve site issues and facilitate trial timelines May be assigned clinical tasks where advanced negotiating skills are required You Are Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field Minimum of 2 years of independent on-site monitoring experience in clinical trials Previous exposure to global oncology studies in Phase I, II, or III Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements Excellent communication, organizational, and problem-solving skills Ability to manage multiple priorities and work independently Willingness to travel as required for site visits What ICON Can Offer You Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Company Description We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device. We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives. Job Description POSITION SUMMARY The Client Quality Assistant supports the Client Quality team with administrative tasks, including but not limited to tracking, document preparation, compliance assessment and project planning. The Client Quality Assistant supports the Client Quality team in ensuring that its activities are managed in compliance with global regulations, legislation and PrimeVigilance requirements. Drives quality and compliance by ensuring tracking of completion of key quality tasks for projects. Role And Responsibilities Key responsibilities include (but are not limited to): Document organisation Data retrieval and tracking for different purposes Conduct periodic training reconciliation and maintenance of training matrix Generate metrics and KPI assessment Prepare documents´ drafts and/or final lay out, as applicable Organise meetings and teleconferences Assist with the organisation of Client Quality department Perform other miscellaneous administrative tasks, as applicable Assistance with preparation of documents for audit/inspection requests Specified Additional Responsibilities Other administrative support as required. The Client Quality Assistant will support the PrimeVigilance Senior Leadership team and the Associate Director of Quality with assigned quality related projects and responsibilities. Qualifications University graduate Advanced English (both spoken and written) Proficiency in all MS-Office applications including Microsoft Word, Excel, and PowerPoint 2-3 yrs of experience in an administrative position involving management and creation of reports Strong communication skills, attention to detail and problem-solving abilities Additional Information We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. We Offer Training and career development opportunities internally Strong emphasis on personal and professional growth Friendly, supportive working environment Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then Ergomed is a great company to join! Quality Integrity & Trust Drive & Passion Agility & Responsiveness Belonging Collaborative Partnerships We look forward to welcoming your application!

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description We are seeking a Senior Specialist, Intellectual Property for our North America Group (NAG). The incumbent will be based in India, and report to the Lead, Intellectual Property Counsel - North America. As a Senior Specialist in the IP department, you will collaborate with US Counsel and internal stakeholders to design and implement IP strategies to advance Dr. Reddy’s interest in providing affordable health care solutions. Roles & Responsibilities Work with US Counsel in managing ANDA, 505(b)(2), BPCIA, and PM(NOC) patent litigations, including post-grant patent office proceedings by developing and implementing claims and defenses. Assist in discovery, witness preparations, and competitive landscape analysis. Identify strategies related to Paragraph IV certifications and Section viii carve-outs. Work with US Counsel and DRL R&D in securing freedom-to-operate for Dr. Reddy’s products, including clearance of Orange Book and unlisted patents for the bulk API, route of synthesis, finished dosage form and polymorphs. Conduct prior art, patentability, landscape and freedom-to-operate searches. Examine patents, file histories, prior art, ongoing litigations, and citizen’s petitions for possible Paragraph IV and related strategies for ANDA and 505(b)(2) products. Develop and provide IP inputs as part of product selection. Provide IP prosecution strategy, including by collaborating with R&D on innovation and drafting patent applications. Conduct IP due diligence and provide IP support towards business development activities. Qualifications Educational qualification: Advanced Degree in pharmaceutics, pharmacology, pharmaceutical chemistry, or similar discipline required (MS or PhD); LLB preferred. Minimum work Experience: 14+ years of experience working with life science, biotechnology, and/or pharmaceutical companies in Intellectual Property is required, wherein 6+ years were spent assisting on complex intellectual property issues for the United States litigations. Skills & attributes: Technical Skills Experience in Intellectual Property (IP) domain Experience developing strategies for and assisting in the management of ANDA litigations in the US Skilled in infringement/invalidity analysis, freedom to operate, filing and prosecution, Market launch analysis. Experience leading product Identification and selection in perspective of complex Injectable, inhalation, OSDs in different geographies. Sound knowledge of technologies used in various dosage forms. Due diligence experience for North America region. Experience with both small molecules and biologics, not required, but preferred Behavioural Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Good Negotiation and Influencing skills. Ability to work collaboratively with Regulatory and cross-functional teams across US - India time zones. People management skills Additional Information Benefits Offered At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Company Description Scholars Scientific Services is a global leader in organizing high-quality conferences, meetings, workshops, symposia, and webinars in various fields, including Pharma, Healthcare, Science, Technology, and Medicine. With teams in the US, UK, Japan, and India, we bring together experts to foster the dissemination of scientific knowledge and research. Our events are renowned for their outstanding scientific quality and informal, interactive settings. Role Description This is a full-time, on-site role for a Program Manager located in Hyderabad. The Program Manager will be responsible for managing and coordinating various programs, including conferences, meetings, and workshops. Day-to-day tasks involve program development, project management, and ensuring excellent customer service. The Program Manager will also be responsible for effective communication within the team and with external stakeholders to ensure the successful execution of all programs. Qualifications Program Management and Program Development skills Project Management skills Excellent Communication and Customer Service skills Ability to work effectively on-site in Hyderabad Bachelor's degree in a related field Experience in the scientific or academic conference industry is a plus Strong organizational and multitasking abilities B. Tech Biotechnology, Msc Microbiology, Pharmacy (B. Pharmacy and M. Pharmacy), Pharm D (Preferably Freshers)

Company Description KIHT Certification Services (KCS) is a division under the Kalam Institute of Health Technology (KIHT) dedicated to certification activities for Medical Device Quality Management System (MDQMS) as per ISO 13485:2016. Supported by the Department of Biotechnology under the Ministry of Science and Technology, KIHT aims to uphold quality standards in the medical device sector. The institution, established in July 2017, is located in Visakhapatnam. Role Description This is a full-time on-site role for a Lead Auditor at KIHT Certification Services. The Lead Auditor will be responsible for conducting audits related to the Medical Device Quality Management System (MDQMS) as per ISO 13485:2016 standards. The role will involve assessing compliance, identifying areas for improvement, and ensuring adherence to accreditation requirements. Qualifications Strong knowledge of ISO 13485:2016 standards and ISO/IEC 17021-1:2015 requirements Experience in auditing Medical Device Quality Management Systems Excellent analytical and problem-solving skills Effective communication and interpersonal skills Attention to detail and ability to work independently Certification as an ISO Lead Auditor is preferred Bachelor's degree in a relevant field, such as Healthcare Quality Management or Auditing

Position – Regional Sales Manager/Key Account Manager Headoffice – Mumbai, Maharashtra Location – Western Line, Mumbai Exp – 8-10 Yrs. Employment Type - Full-time | Senior-Level | B2B Sales | Technical Knowledge Required Key Responsibilities: Drive revenue growth by managing and expanding key accounts in large bakery organizations and food manufacturing units. Develop strategic partnerships with senior stakeholders and decision-makers. Sell bakery ingredients in bulk quantities, focusing on technical products like enzymes, improvers, and emulsifiers. Deliver technical product presentations and support product trials in collaboration with R&D and application teams. Identify new business opportunities and create tailored solutions for each client. Negotiate long-term contracts and ensure consistent client satisfaction and retention. Monitor market trends, competitor activities, and client feedback to inform sales strategy. Prepare detailed reports, forecasts, and strategic plans for senior management Qualification: Bachelor’s degree in Food Technology, Biotechnology, Business, or related field; a technical background is a strong plus. 8–10 years of experience in B2B sales, preferably with a focus on technical food ingredients. In-depth understanding of bakery raw materials and enzyme-based products. Proven ability to handle senior-level stakeholders and large accounts. Excellent verbal and written communication skills. Strong analytical thinking, presentation, and negotiation capabilities. Familiarity with Mumbai's Western Line market and client base is an advantage. Willingness to travel locally and occasionally regionally. Please contact - Saanvi Gandhi saanvi@hrpc.in | 77108 44668 - Wats app

About Us: We are a leading engineering firm specializing in the design and construction of state-of-the-art HVAC systems and controlled environments. We are committed to delivering innovative and efficient solutions for our clients in the pharmaceutical, biotechnology, semiconductor, and other high-tech industries. We are currently seeking a highly motivated and experienced HVAC and Cleanroom Design Engineer to join our dynamic team. Job Summary: The HVAC and Cleanroom Design Engineer will be a key member of our project team, responsible for the design, engineering, and cost estimation of HVAC and cleanroom systems. The ideal candidate will have a strong background in mechanical engineering, a deep understanding of cleanroom standards, and proven experience in delivering cost-effective and compliant designs. Key Responsibilities: System Design and Engineering: Develop detailed HVAC and cleanroom system designs, including airflow diagrams, piping and instrumentation diagrams (P&IDs), and ductwork and piping layouts. Perform heating, ventilation, and air conditioning (HVAC) load calculations to determine system capacity and specifications. Select appropriate HVAC equipment, such as air handling units (AHUs), chillers, boilers, and fans, based on project requirements and energy efficiency goals. Design critical environments to meet specific ISO 14644 classifications, ensuring proper air change rates, pressure cascades, and filtration levels (HEPA/ULPA). Prepare comprehensive design documentation, including technical specifications, drawings, and schedules using AutoCAD, Revit, and other design software. Cost Estimation and Budgeting: Develop accurate and detailed cost estimates for HVAC and cleanroom projects, including equipment, materials, labor, and subcontracted services. Analyze project specifications and drawings to identify potential cost-saving opportunities and value engineering options. Prepare and present budget proposals to project managers and clients. Track project costs and provide regular updates on budget adherence. Standards and Compliance: Ensure all designs comply with relevant industry standards and regulations, including but not limited to: ISO 14644: Cleanrooms and associated controlled environments. ASHRAE: Standards for ventilation, energy efficiency, and indoor air quality. SMACNA: Sheet Metal and Air Conditioning Contractors' National Association standards for ductwork construction. Good Manufacturing Practices (GMP): As applicable to pharmaceutical and biotech facilities. Stay current with the latest advancements in HVAC technology, cleanroom design, and industry best practices. Project Collaboration and Support: Collaborate effectively with architects, structural engineers, electrical engineers, and other project stakeholders to ensure an integrated and coordinated design. Provide technical support and guidance to the construction and commissioning teams. Review and approve submittals from vendors and subcontractors. Participate in project meetings and site inspections as required. Qualifications and Skills: Bachelor's degree in Mechanical Engineering or a related field. Proven experience in HVAC system design, with a strong portfolio of cleanroom projects. In-depth knowledge of cleanroom design principles, including contamination control, airflow dynamics, and filtration. Demonstrated experience in cost estimation and budgeting for mechanical systems. Proficiency in AutoCAD, Revit, and HVAC load calculation software. Thorough understanding of relevant industry standards (ISO 14644, ASHRAE, SMACNA, GMP). Excellent analytical, problem-solving, and decision-making skills. Strong communication and interpersonal skills, with the ability to work effectively in a team environment. What We Offer: Competitive salary and benefits package. Opportunities for professional development and career growth. A collaborative and innovative work environment. The chance to work on challenging and rewarding projects that make a difference.

Company Description: SD BIOSENSOR is a company specialized in in-vitro diagnostics founded with the goal of contributing to improving the quality of life through fast and accurate diagnosis of disease. Role Description This is a full-time on-site role for a Product Executive , located in Gurugram for IVD division Marketing team . The Product Executive will be responsible for conducting market research and analysis to identify trends and opportunities. Key Responsibilities: 1. Product Development: - Develop and launch new diagnostic products ( Rapid and ELISA tests ). - Collaborate with cross-functional teams (R&D, QA, Regulatory, Finance). 2. Market Analysis: - Conduct market research to identify trends, competitors, and customer needs. - Analyze market data for product development and marketing strategies. 3. Create promotional materials and campaigns. Requirements: 1. Education: Bachelors/ Master's degree in Life Sciences, Biotechnology, Marketing or related field. 2. Experience: Minimum 5-6 years in product management, diagnostic industry experience preferred. 3. Skills: - Strong understanding of diagnostic testing principles. - Excellent communication skills, Sound knowledge of Excel and PowerPoint, and analytical skills. -Experience in Market Research and Market Analysis Interested Candidate Can share resume at- nidhi.mishra@sdbiosensor.co.in

Company Description

Shaiva Group drives success in fintech, biotechnology, and real estate products for its clients. With a focus on delivering innovative solutions, Shaiva Group prides itself on helping clients achieve their goals. The company's diverse portfolio and commitment to excellence make it a leader in its industry. Happiness is Success!

Role Description

This is a full-time on-site role for an Executive Assistant located in Dubai, United Arab Emirates. The Executive Assistant will be responsible for providing comprehensive executive support, handling administrative tasks, managing expense reports, and effectively communicating with internal and external stakeholders. Daily tasks also include managing schedules, organizing meetings, and ensuring smooth office operations.

Qualifications

• Executive Administrative Assistance and Administrative Assistance skills
• Experience in managing Expense Reports
• Strong Executive Support skills
• Excellent Communication skills
• Attention to detail and organizational skills
• Ability to handle confidential information with discretion
• Proficiency with office software and scheduling tools
• Good skill-level at creating business presentations
• Bachelor's degree or equivalent experience in a relevant field

Company Description Shaiva Group drives success through fintech, biotechnology, and real estate products. Our commitment to "Happiness is Success" ensures we deliver innovative solutions to our clients. Join us to help shape the future by leveraging advanced technologies and industry expertise. Located in Dubai, United Arab Emirates, we aim to be at the forefront of industry advancements. Role Description This is a full-time, on-site role for a BFSI Business Analyst located in Hyderabad, India. The Business Analyst will be responsible for analyzing business processes, gathering and defining business requirements, and performing data analysis. Day-to-day tasks include collaborating with stakeholders, documenting business processes, identifying opportunities for improvement, and ensuring that business requirements are met. The role requires strong problem-solving skills and the ability to communicate effectively with team members and clients. Qualifications Strong Analytical Skills Proficiency in Business Analysis Excellent Communication Skills Experience with Business Processes and improving them Capability to define and manage Business Requirements Ability to work collaboratively in a team environment Relevant industry certifications (e.g., CBAP, PMI-PBA) are a plus Bachelor's degree in Business, Finance, or related field

As an Assistant Professor (Research) in Agricultural Biotechnology at Peoples University in Bhopal, India, you will be responsible for conducting independent and collaborative research in your field. Your key responsibilities will include developing and leading research projects, securing research funding, and publishing in high-impact journals. Additionally, you will have the opportunity to mentor postgraduate and Ph.D. students in their research work, collaborate with academic and industry partners, and contribute to the development of innovative teaching methods and materials. To qualify for this position, you must hold a Ph.D. in Agricultural Biotechnology from a recognized university, along with 2-3 years of postdoctoral research experience in relevant areas. A strong record of research publications in peer-reviewed journals, proven experience in securing research grants, and excellent communication and interpersonal skills are essential. Your commitment to academic excellence and passion for teaching and research will be highly valued in this role. In return, Peoples University offers a competitive salary and benefits package, access to state-of-the-art research facilities, opportunities for professional development and collaboration, and a supportive and vibrant academic environment. If you are ready to shape the future of Biotechnology at Peoples University, we invite you to apply by submitting your detailed CV, cover letter, research statement, and contact information for three professional references to garima.hr@peoplesuniversity.edu.in and deepu.hr@peoplesuniversity.edu.in. Applications will be accepted until the positions are filled. Peoples University is an equal-opportunity employer, welcoming candidates of all backgrounds and experiences to join us in this exciting opportunity. This is a full-time position with a day shift schedule, and candidates must be willing to commute or relocate to Bhopal, Madhya Pradesh. Experience: 1 year (Preferred) Work Location: In person,

Company Description Eminent Biosciences (EMBS) is a Bio-Healthcare Informatics Research Organization located in Indore, India. EMBS provides innovative solutions in Bioinformatics, Computational Biology, developing top-notch software and databases for research in the Life Sciences, Health care and the Pharmaceutical Industries. Our offerings include Next Generation Sequencing (NGS) data analysis, Healthcare data analysis, and Epidemiological Data analysis using Machine Learning and Artificial Intelligence for both automatically curated and manually curated data. We also provide industry-driven training, diploma courses, and PhD programs related to Bioinformatics and Computational Biology affiliated with a few universities in India. Role Description This is a full-time hybrid role as a PhD supervisor at Eminent Biosciences, located in Indore, with some flexibility for work from home. The Scientist/Professor will be responsible for designing and delivering research materials, developing curriculum, assessing students' research progress, and providing feedback. Responsibilities also include mentoring students, conducting research, and contributing to the development of PhD Bioinformatics programs. Collaboration with colleagues and continuous professional development are key aspects of this role. Qualifications PhD degree in Bioinformatics, Computational Biology, or a related field Proven experience as a Bioinformatics or Biotechnology Professor in Academics or a Scientist in industry Strong background in Biosciences, Bioinformatics, or related fields Skills in Bioinformatics, R Programming, Python, Next Generation Sequencing, Machine Learning and using cloud computing technologies and software Minimum 5 Research Paper publications as a corresponding author in SCI journals. Excellent communication, mentoring, and organizational skills Ability to work collaboratively and independently Experience in the Healthcare/Biotechnology/Bioinformatics/Pharma or life sciences industry/academics is a plus

Alpha Coding Solutions | MNC Placement | Day Shift | Life Science Graduates Locations : Chennai, Coimbatore, Salem, Trichy, Nagercoil, Tirunelveli, Vellore, Villupuram + Telangana, AP, Karnataka, Kerala Apply via Email : karthialphahr@gmail.com WhatsApp Resume : 9042912356 Contact HR Karthiga : 9150485077 Role Overview Join leading healthcare BPOs as a Medical Coder . You'll be responsible for translating clinical data into standard codes using ICD-10-CM, CPT, and HCPCS , supporting global medical documentation standards. Eligibility Qualifications : Diploma / UG / PG in any of the following: Life Sciences: Biotech, Microbiology, Biochemistry, Zoology, Botany, Biomedical, etc. Paramedical: BDS, BPT, BHMS, BAMS, BSMS, Nursing, GNM, MLT, Pharmacy, etc. Allied Health: Radiology, Dialysis, Cardiac Tech, Respiratory Therapy, Optometry, Clinical Nutrition, and more. Age Limit : Below 29 years Freshers & Experienced candidates welcome Salary & Benefits 13,000 18,000/month for freshers Up to 50,000/month for experienced candidates 4,000 fixed hike after 6 months Performance-based incentives & appraisals Food & cab (based on client company) Medical insurance, PF, Gratuity, Referral bonus 5-Day Work Week | Day Shift | Sat & Sun Off Career in a Global Healthcare MNC Starts Here! Stable Job | Career Growth | Professional Work Environment Apply Now Send your resume to karthialphahr@gmail.com Or WhatsApp: 9042912356

Description At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview This is a hands-on, non-supervisory position in USP-India's Biologics laboratory. In this position, the scientist will spend 80-100% of the time in laboratory and will perform bioassays and binding for various biologics product class such as recombinant proteins and mAbs, perform vaccine and cell and gene therapy (CGT) functional characterization assays, and viral assays. Scientist will be responsible for hands-on execution of projects which can be collaborative testing of reference standards, characterization of biological products, method development and validation for development of standards (Documentary Standards, Physical Reference Standard & Performance Standards). Responsible for supporting activities related to India Biologics laboratory. How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. Proficient in in vitro cell based relative potency. Proficient in handling cell lines and primary cells. Experienced in functional activity and immunogenicity assays. Proficient in flow cytometry. Experienced in method qualification and validation, protocol, report writing and data presentation. Plans and executes research projects independently. Evaluates and analyzes scientific reports and identifies next steps and key challenges. Works with cross-functional teams within the organization to solve/support both technical and process-related issues. Performs peer-review of collaborative testing reports and research reports. Keeps abreast of current trends and developments in related scientific field. Shares technical expertise with junior colleagues and serves as a mentor for them Seeks out innovative ways to apply knowledge or skills to improve protocols and results Assists team lead in planning, implementing, and evaluating laboratory procedures/systems Supports in departmental trainings as applicable. Attends scientific seminars and conferences Supports lab management activities Follows GLP and QMS practices. Recommend improvement to systems and all other supporting activities as assigned by the team lead. Participates in internal and external audits. Aligns with USP's mission, and complies with USP's guidelines and other requirements Performs other duties as assigned. Who is USP Looking For? Example The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: MSc. in Biochemistry, or related Biological Science field with 6-8 years of Industrial experience in bio pharmaceutical product development and quality testing, relative potency assays, mAb functional assays, expertise in flow cytometry, and primary cell culture. Able to analyze and interpret data using appropriate statistical software/methods and calculation for relative potency determination. An equivalent combination of education and experience may be substituted. Laboratory experience must include expertise developing and validating assays, and QMS knowledge and experience. Additional Desired Preferences Working experience in the biotechnology/biopharmaceutical industry strongly preferred. Demonstrated research, technical, and analytical skills, as well as the ability to take highly technical scientific information and make recommendations. Ability to learn new technologies and strong computer, scientific, and organizational skills. Good written and verbal communication skills, time management skills as well as interpersonal skills. Results driven with demonstrated successful outcomes. Individual must possess the ability to handle multiple priorities in fast-paced environment. Knowledge/participation of reference standards development related to bio pharmaceutical products/industry. Experience with reference materials development is a plus. Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time

Responsibilities: Experience in sales and Applications operations Proficient laboratory skills Bachelor's degree in Life Sciences, Biotechnology 0-2 years of experience in application sales Must be prepared to travel south and north Indian Cities Mobile bill reimbursements Travel allowance

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: The Director, Information Systems is responsible for leading and charting the course for Reporting, BI, and Sensing products and services team that builds and transforms technology capabilities that positively impact business outcomes. This individual will be responsible for developing and leading a highly talented team that is built for delivering high-end and innovative technologies. The ideal candidate will have a proven track record of leadership in technology-driven environments for the Enterprise Sensing area and has a passion for fostering innovation and excellence in the biotechnology industry. Additionally, collaboration with cross-functional and global teams is required to ensure seamless integration and operational excellence. The ideal candidate will have a strong background in Analytics Solutions, the end-to-end software development lifecycle and a Scaled Agile practitioner, coupled with leadership and transformation experience. This role demands the ability to drive and deliver against key organizational strategic initiatives, foster a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Roles & Responsibilities: Maintain strategic relationships and strong communication with the leadership team about IS services and service roadmaps to ensure that all stakeholders feel informed and engaged. Lead and manage large, diverse teams within a matrixed organization. Collaborate with geographically dispersed teams, including those in the US and other international locations. Oversee the software development lifecycle for effective execution and delivery. Develop and implement strategic plans for technology and workforce. Follow global standards and practices set up at Amgen. Foster a culture of collaboration, innovation, and continuous improvement. Attract and recruit top talent as part of an extensive Technology organization to be hired within India. Develop talent, motivate the team, delegate effectively, champion diversity within the team, and act as a role model of servant leadership. Responsible for managing, growing, and developing the Amgen Technology team in India, ensuring global ways of working are embedded in the local organization. Understand the decision-making process, workflows, and business and information needs of business partners and stakeholders. Contribute and define business outcomes + requirements, technology solutions, and services. Improve activities being measured by crafting, monitoring, and optimizing relevant feedback loops through 'test & learn' activities. Work with Product Owners, Service Owners, and/or delivery teams to ensure that delivery matches commitments, acting as an escalation point and facilitating communication when service commitments are not met. Ensure communication of key performance metrics and analysis of unmet needs. Participate in stakeholder and other leadership meetings, working with other parts of the organization, and functional groups to ensure successful delivery. Ensure ongoing alignment with strategy, compliance, and regulatory requirements for technology investments and services. Facilitate best practice sharing, ensuring ongoing alignment with the Technology & Digital strategy. Oversee operating budgets and product team budgets, ensuring regular review of actuals and latest estimates, managing according to agreed governance. Ensure alignment of Technology service plans across the organization. Remain accountable for ensuring overall organizational compliance to quality/compliance requirements such as GXP and Privacy. Basic Qualifications and Experience: 18 to 23 years of experience with 8+ years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources AND Doctorate Degree / Master’s degree / Bachelor’s degree in Business, Engineering, IT, or related field Functional Skills: Leadership: Influences through Collaboration: Builds direct and behind-the-scenes support for ideas by working collaboratively with others. Strategic Thinking: Anticipates downstream consequences and tailors influencing strategies to achieve positive outcomes. Transparent Decision-Making: Clearly articulates the rationale behind decisions and their potential implications, continuously reflecting on successes and failures to enhance performance and decision-making. Adaptive Leadership: Recognizes the need for change and actively participates in technical strategy planning. Must-Have Skills: Demonstrated experience in managing technology initiatives and teams with a track record of successful innovation. Specifically, teams leveraging Business Intelligence tools, software engineering, and leveraging AI in analytics. Experience in people management and leading matrixed teams, and passion for mentorship, culture, and fostering the development of talent. Must be flexible and able to manage multiple activities and priorities with minimal direction in a rapidly changing and demanding environment. Exceptional collaboration, communication, and interpersonal skills to effectively manage stakeholder relationships and build new partnerships. Experience in applying technology best practice methodologies: Scaled Agile (SAFe), ITIL, etc. Have strong business acumen. Can demonstrate deep understanding of industry, therapy, and product. Good-to-Have Skills: Experience in a leadership role within a pharmaceutical or technology organization. Extensive experience in the software development lifecycle. Experience using and adoption of Scaled Agile Framework (SAFe). Strong analytic/critical-thinking and decision-making abilities. Ability to work effectively in a fast-paced, dynamic environment. Established business partnerships and IS governance practices involving senior business stakeholders. Broad working knowledge of key IS domains and layers. Professional Certifications (please mention if the certification is preferred or mandatory for the role): ITIL (preferred) Scaled Agile Framework (SAFe) for Teams Soft Skills: Excellent leadership and team management skills. Strong transformation and change management experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. Excellent analytical and troubleshooting skills. Strong verbal and written communication skills. Ability to work effectively with global, virtual teams. 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. 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.

We are looking for a serious candidate for taking care of the company's CEO Health, Fitness, Food & Diet Plans. Due to 10-12 hrs of Daily Straight Work, Our CEO needs someone who can prepare a diet plan, make food arrangements and take care of the CEO's health & his medicines. Someone who knows the basics of Rehabilitation and pain management therapy, MS office & can work as his primary work assistant. Eligibility Criteria: Qualification: Freshers/ Experienced with Degree in Either of Nursing, Life science graduates, Pharmacy, Physician assistant, Biomedical Engineers, Biochemistry, Bio technology, Bioinformatics, Micro biology, Zoology and Advanced zoology, Biology, Botany, Plant biotechnology, Food and Nutrition, Paramedical, Physiotherapy, Any Graduate, Any Post Graduate, BSc, MSc, Diploma, 12th Pass, 10th Pass Must be Fluent in Either English or Hindi Communications Ready to Work from Bangalore Office (Work from Office) Should able to Join Immediately/ Within a Week Knowledge in Preparing Food, Nutrition and Diet Planning Knowledge of Rehabilitation and pain management therapy Should able to treat basic issues such as strains, back pain and posture problems Ready to Travel in/ out of the city as per company needs Basic Computer, MS Office, MS Word, Excel Knowledge Only female candidate will have to apply for this post Key Roles & Responsibilities: Taking care of CEOs Food, Health, Diets, Fitness, Workouts Ensuring Regular Exercise, Medications, Be Health Consciousness for CEO Preparing Regular Breakfasts, Lunch, Snacks and Dinner as per Diet Plan In case of Travel, Hotel Bookings and Making Outside Food Arrangements CEOs personal Works like Shopping, Reminders and Transportation etc Treating issues such as strains, back pain and posture problems A Genuine Passion for Caring Elders & Moral Work Ethics Basic Computer, MS Office, MS Word, Excel Works Job Location: New Airport Rd, Kothanur, Bangalore Working Hours: 8AM-6PM or 10AM-8PM (2 hrs lunch break) Salary & Benefits: Monthly Rs 25,000-40,000 (depends on interview/ experiences) For Quick process, Whatsapp your CV/Details to HR ( 7259607911) OR Send your CV to Email: satyamquestapps@gmail.com

Job Description Position Title, Responsibility Level: Executive/Senior Executive Function: Operations Reports to - Assistant Manager/Lead Assistant Manager Permanent/ Temporary: Permanent Span of Control – None Location: C – 15, Noida Basic Function This position is responsible for reviewing, analyzing and interpreting medical Information to assess and determine appropriate next action steps which may lead to denial or payment of claims. Work is performed under general supervision according to established guidelines. This individual promotes capabilities from a customer perspective, aligning needs with the target offering by creating a customer self-service enabled platform for core customers. Essential Functions Responsible for reviewing and analyzing discrepancies by cross-verifying from different data sources Familiar with US Healthcare domain knowledge and understanding of healthcare regulations (HIPAA) Deep understanding of medical coding, billing, and medical terminologies Attention for detail, and Strong analytical skills for processing medical documentation Critical thinking and high independent decision making capability Proficiency in healthcare information systems Ability to navigate through multiple applications Operates with urgency in a real time service environment Meets individual goals while assisting team to meet team goals Defines, communicates and manages workflow and data coordination to support various implementation related reports (i.e., reporting, inventory, capacity reporting, and ad-hoc reports as needed by management) May perform other duties as assigned Performance parameters Productivity Quality Turn Around Time of work assigned Attendance & Schedule Adherence Primary Internal Interactions SME/AM/LAM/Manager for the purpose of reporting performance, escalation handling, clarifying concerns, and seeking support AM/LAM for the purpose of settling issues left unresolved by the SME and monthly evaluation of performance SME for the purpose of handling process related issues; queries and escalated transactions QCA for the purpose of associate performance feedback and audit in order to update the training curriculum Mentors for the purpose of seeking clarifications and answering queries real time Organizational Relationships Reports To: Assistant Manager/Lead Assistant Manager Skills Desirable Skills Critical thinking and high independent decision making Strong analytical, Reasoning, and Problem solving skills Medium competency in excel skills Ability to comprehend and write in English for structured written communications. Emails/IMS to be sent to internal teams Ability to respond to all inquiries within a timely manner Strong interpersonal and communication skills – both verbal and written Adaptability/Ability to interpret variable input details Technical Skills Good computer navigation skills Typing speed of 25 Words per Minute with 90% Accuracy Proficiency in healthcare information systems Ability to navigate through multiple applications Process Specific Skills Familiar with US Healthcare domain knowledge and understanding of healthcare regulations (HIPAA) Deep understanding of medical coding, billing, and medical terminologies Ability to produce high quality in production in environment. Ability to troubleshoot, identify user errors vs. system mapping errors (enrollment dates, method, system logic) Soft Skills Ability to work independently Ability to understand and question established process guidelines for possible process improvements Attention for detail, and Strong analytical skills for processing medical documentation Possess keen sense of acquiring knowledge Adaptable and flexible to work in night shifts Education Requirements And Work Experience Bachelor’s degree in relevant field such as Biology, Biochemistry, Biotechnology etc Computer literacy Candidates with relevant business experience will be preferred Annexure Acknowledgement (acknowledge that the information contained in this document is factual and complete) ________________ Candidate Supervisor Date

1. Assist intervention in cath lab. 2. Manage the usage of the supplies and inventory and sterilization of consumables. 3. Archiving of clinical data 4. Maintain, utilize provide the right hardware during procedures. 5. Take necessary actions during emergencies. 6. Prior to surgery, ensure the EKG equipment is in working order, and during the procedure, monitor the EKG readouts, and keep the doctor apprised of anything considered abnormal. 7. Prepare the patient for the procedure by cleaning, shaving, and, in the case of cardiac catheterization for angioplasty, anesthetizing the area of insertion. 8. Maintain Cath-lab equipment 9. Inform patients regarding procedures to reduce anxiety 10. Reuse of material by sterilization and aseptic measures 11. Haemodynamic monitoring of patients 12. Round the clock availability for patient care 13. Adherence to Quality and Safety standards as per SOP.

Role: Cath Lab Technician Type: Full Time Job description 1. Assist intervention in cath lab. 2. Manage the usage of the supplies and inventory and sterilization of consumables. 3. Archiving of clinical data 4. Maintain, utilize provide the right hardware during procedures. 5. Take necessary actions during emergencies. 6. Prior to surgery, ensure the EKG equipment is in working order, and during the procedure, monitor the EKG readouts, and keep the doctor apprised of anything considered abnormal. 7. Prepare the patient for the procedure by cleaning, shaving, and, in the case of cardiac catheterization for angioplasty, anesthetizing the area of insertion. 8. Maintain Cath-lab equipment 9. Inform patients regarding procedures to reduce anxiety 10. Reuse of material by sterilization and aseptic measures 11. Haemodynamic monitoring of patients 12. Round the clock availability for patient care 13. Adherence to Quality and Safety standards as per SOP.

1. Assist intervention in cath lab. 2. Manage the usage of the supplies and inventory and sterilization of consumables. 3. Archiving of clinical data 4. Maintain, utilize provide the right hardware during procedures. 5. Take necessary actions during emergencies. 6. Prior to surgery, ensure the EKG equipment is in working order, and during the procedure, monitor the EKG readouts, and keep the doctor apprised of anything considered abnormal. 7. Prepare the patient for the procedure by cleaning, shaving, and, in the case of cardiac catheterization for angioplasty, anesthetizing the area of insertion. 8. Maintain Cath-lab equipment 9. Inform patients regarding procedures to reduce anxiety 10. Reuse of material by sterilization and aseptic measures 11. Haemodynamic monitoring of patients 12. Round the clock availability for patient care 13. Adherence to Quality and Safety standards as per SOP.

1. Assist intervention in cath lab. 2. Manage the usage of the supplies and inventory and sterilization of consumables. 3. Archiving of clinical data 4. Maintain, utilize provide the right hardware during procedures. 5. Take necessary actions during emergencies. 6. Prior to surgery, ensure the EKG equipment is in working order, and during the procedure, monitor the EKG readouts, and keep the doctor apprised of anything considered abnormal. 7. Prepare the patient for the procedure by cleaning, shaving, and, in the case of cardiac catheterization for angioplasty, anesthetizing the area of insertion. 8. Maintain Cath-lab equipment 9. Inform patients regarding procedures to reduce anxiety 10. Reuse of material by sterilization and aseptic measures 11. Haemodynamic monitoring of patients 12. Round the clock availability for patient care 13. Adherence to Quality and Safety standards as per SOP.

Long Description R&D Document control - Document storage, arrangement, and enhance traceability. Contribute to system improvement for document traceability without error/gap Review of R&D documents as per quality compliance along with raw data/metadata review and electronic data verification on systems as per requirement Issuance, submission/archival: Issuance, submission/archival of logbooks, LNBs, documents (including soft/electronic document control) Equipment & CSV related document review (IQ, OQ, PQ etc. ) Respective document archival, submission and maintain traceability of all documents QAMS review support for evaluation of QAMS elements such as Deviation, Change Control, CAPA, LIR etc. Any responsibility advised by superior from time to time Competencies Collaboration Customer Centricity Developing Talent Innovation & Creativity Process Excellence Result Orientation Stakeholder Management Strategic Agility Education Masters in Biotechnology Post Graduation in Biotechnology Work Experience 2-4 years of experience

Job Description Physical verification and readiness of equipment and instrument for process. Arranging the process accessories and consumables in process area before batch execution. Coordination for dispensing of raw material required for the production processes. Preparation of process, equipment and area related SOPs and EOP s. Preparation of process, area and equipment qualification/ validation protocols. Preparation and execution of various reports like process, equipment, area qualification and validation. Request and Issuance of BPR. Preparation and review of BPR. Preparation and execution of study protocols, URS as and when required Work Experience 4 to 7 Years in Downstream processing. Education Masters in Biotechnology or Biochemistry B. Tech in Biotechnology or Biochemistry Competencies

Company Description Titan Biotech Ltd. is a leading manufacturer and exporter of biological products used in various industries including Pharmaceutical, Nutraceutical, Food & Beverages, Biotechnology, and more. The company focuses heavily on research and development to innovate new biological products. Certified by ISO 9001:2008 and cGMP facilitated, Titan Biotech offers high-quality products including protein hydrolysates, culture media, laboratory chemicals, and plant growth promoters. With its products recognized for clinical diagnosis and microbiology, Titan Biotech has a global footprint, exporting to 35 countries. Role Description This is a full-time, on-site role for an Area Sales Manager based in Baroda. The Area Sales Manager will oversee daily sales operations in the designated region, manage and support the sales team, develop and execute sales strategies, and work to achieve sales targets. Responsibilities also include market analysis, maintaining customer relationships, and ensuring customer satisfaction. Qualifications Sales and Marketing skills for developing and executing sales strategies Ability to conduct Market Analysis and identify growth opportunities Strong customer relationship management and communication skills Leadership skills to manage and support a sales team Bachelor's degree in Business, Marketing, or related field Experience in the biotechnology or pharmaceutical sectors is a plus Excellent problem-solving skills and ability to work independently