3619 Biotechnology Jobs - Page 24

Internship Summary: We are seeking a motivated and detail-oriented Product Specialist Intern to join our team. This role provides a unique opportunity to gain hands-on experience in the medical device industry, working closely with R&D and other departments. As an intern, you will assist in product development, market research, and client support activities, helping to ensure our devices meet the highest standards in clinical application and user satisfaction. Key Responsibilities: Support R&D team in developing and refining medical devices. Assist in product testing, usability studies, and gathering feedback from healthcare professionals. Help prepare product documentation, including technical specifications, training materials, and user manuals. Assist with troubleshooting and resolving customer inquiries related to product functionality and usage. Qualifications: Currently enrolled in a Bachelor’s or Master’s program in Biomedical Engineering, Biotechnology or a related field. Strong interest in medical devices and healthcare technology. Excellent research, analytical, and problem-solving skills. Strong verbal and written communication skills . Ability to work collaboratively in a team environment and manage multiple projects. Basic knowledge of medical terminology and regulatory standards is a plus. What We Offer: Hands-on experience with cutting-edge medical device technology. Mentorship and guidance from experienced product specialists and R&D professionals. Opportunity to contribute to real-world projects that impact patient care. Networking opportunities and career development resources. Stipend: This internship offers a monthly stipend of ₹10,000 for the duration of the 3-month period with potential for full-time employment based on performance No .* Of Opening: 2* Who can apply? Recent graduates from the 2025 batch who are interested in building a career in healthcare technology. Send your resume to : hrm@vrpmedgands.com/9597123526 Job Type: Full-time Pay: Up to ₹10,000.00 per month Benefits: Commuter assistance Flexible schedule Leave encashment Paid sick time Paid time off Application Question(s): Are you comfortable to travel within cochin, kerala? Education: Bachelor's (Preferred) Language: English (Required) Willingness to travel: 50% (Preferred) Work Location: In person Expected Start Date: 23/07/2025

Job Summary: We are seeking a responsible and experienced Lab Incharge to oversee the daily operations of our laboratory. The ideal candidate will ensure that all laboratory functions run smoothly, maintain quality standards, and comply with safety protocols. This role involves supervision of lab staff, inventory management, maintaining records, and ensuring timely reporting of test results. Key Responsibilities: Supervise all laboratory operations and ensure smooth day-to-day functioning. Manage and coordinate the lab staff, assigning duties and ensuring adherence to protocols. Ensure the accuracy, reliability, and timely delivery of all laboratory reports. Monitor laboratory equipment and arrange for routine maintenance and calibration. Maintain inventory of lab supplies, chemicals, and reagents; place orders as needed. Implement and monitor quality control procedures. Ensure all lab practices are in compliance with health and safety regulations. Provide training and guidance to laboratory technicians and assistants. Maintain accurate documentation and records of test results, calibration, and maintenance logs. Collaborate with doctors/medical professionals for interpretation of test results (if applicable). Participate in audits and implement corrective actions when necessary. Stay updated on new testing techniques, equipment, and procedures. Qualifications: Bachelor’s or Master’s degree in Medical Laboratory Technology, Biotechnology, Microbiology, or a related field. Minimum [2-3] years of experience in a laboratory setting, with at least 1 year in a supervisory or incharge role. Strong knowledge of laboratory safety and quality protocols. Familiarity with laboratory information systems (LIS). Excellent organizational and leadership skills. Attention to detail with good analytical and problem-solving abilities. Strong communication and interpersonal skills. Preferred Skills: Experience with NABL or ISO accreditation standards. Basic knowledge of biomedical waste management. Ability to manage team performance and resolve conflicts effectively. Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Schedule: Day shift Work Location: In person

Job Description About the Company: Pharmintech Turnkey Solutions Pvt. Ltd. is a technology-driven, information focused organization dedicated to delivering the highest quality cleanroom solutions at competitive prices. Our strategic vision is to continuously introduce advanced technologies in the cleanroom industry and ensure timely delivery of innovative solutions. We specialize in manufacturing and supplying pharmaceutical cleanroom projects, offering turnkey solutions to contractors across Mumbai, India, and globally, adhering to the latest international standards. Our commitment to excellence and quality drives us to deliver defect-free and reliable products that are in high demand across Pharmaceutical, Cosmetics, Biotechnology, and Food industries worldwide. Our core team comprises highly motivated professionals with strong academic and technical backgrounds, equipped with deep knowledge of business development, engineering, and quality management. Our team of experienced engineers oversees all operations including production, quality control, and product development. At Pharmintech, our goal is to achieve customer satisfaction by understanding their needs, ensuring safety, and continually upgrading our products and services. Job Overview: Company Name: Pharmintech Turnkey Solutions Pvt. Ltd. Head Office Location: Thane, Mumbai Job Location: Ahmedabad, Gujarat (Remote) Designation: Sales Engineer No. of Positions: 01 Qualification: B.E./B.Tech/ Diploma Employment Type: Full-Time Job Description: We are seeking a highly motivated Sales Engineer with prior experience in the Cleanroom , HVAC , or Pharmaceutical Industry . The ideal candidate will play a key role in developing customer relationships, supporting marketing and sales activities, and achieving sales targets. Key Responsibilities: Client Communication & Relationship Building · Engage with target audiences to establish, maintain, and enhance customer relationships. · Act as a point of contact to address client needs and queries promptly. Marketing Support · Assist the Marketing Manager in executing planned marketing campaigns and initiatives. · Participate in brainstorming and implementing marketing strategies to enhance brand visibility. Sales & Lead Management · Generate new business inquiries and follow up on leads to convert them into sales. · Prepare and submit offer and follow up with the clients and close orders with help of seniors. · Achieve assigned sales targets through strategic planning and execution. Follow-Up & Coordination · Ensure timely payment follow-ups and maintain healthy business relations with clients. · Coordinate with internal teams and clients to ensure smooth execution of orders. Exhibition & Event Participation · Plan and arrange for participation in exhibitions and trade shows. · Represent the company professionally and generate leads during events. Field Visits & Client Meetings · Travel to other cities as required for client meetings, site visits, or promotional activities. · Foster long-term business relationships through in-person interactions. Regional Site Support · Provide coordination and support for ongoing projects and operations at the Gujarat site. Eligibility Criteria · Education: Diploma / Graduate in Engineering disciplines · Industry Background: Must be from Cleanroom, HVAC, or pharmaceutical industry · Experience: Minimum 2+ years · Candidate should know Gujarati language Preferred Industry Experience: · Cleanroom Projects · HVAC Industry · Cosmetic What We Offer: · Competitive salary structure · Opportunity for career advancement · Supportive and skilled team environment · Continuous training and professional development. Salary & Application Process: Salary: As per industry standards How to Apply: Send your updated resume to hr@pharmintech.net. with the subject: Sales Engineer - Ahmedabad Application – [Your Name] Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Leave encashment Paid sick time Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: Remote Expected Start Date: 31/07/2025

Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com. Job Description The Senior Clinical Data Coordinator (Sr. CDC) is a key member of the Development Operations, Data Management Team. The Senior Clinical Data Coordinator will provide data management support for all assigned studies. The Sr. CDC prepares, validates, processes, and maintains clinical data in support of submissions to international regulatory agencies or publication of manuscripts through the use of EDC and SAS software. Assist in the development of edit specifications, based on any available global medical standards, therapeutic area standards, and the protocol, used to clean the study. Performs user acceptance testing (UAT) on eCRF build and edit specifications. Creates supporting DM process documentation to LDM and/or performs peer review of documentation, including updating documentation. Support the coding schedule defined in the data management plan. Collaborate with data coding specialists on a regular basis to guarantee timely coding. Supports/maintains quarterly coding review cycles. Performs manual data listing reviews and submits queries as appropriate. Assist with and/or performs user acceptance testing of lab data standards. Evaluates quality of lab data entry and addresses inconsistencies with sites and CRAs as applicable. Assists in the SAE reconciliation process. This may include coordination with medical experts and Global Drug Safety. Follow up on discrepancies and resolve so both databases are consistent. Applies criteria for subject stage gate of No More Issues (NMI). Also, must coordinate and review medical and statistical queries and certify they are adequately resolved. Assist in the development of a blind review report and conducting a blind review meeting to assign patient validity. Assist in developing and generating study report listings according to ICH and if present company guidelines. Coordinate the query management system functions. Perform the final patient review and database lock activities. Assist in coordinating the processing of scheduled data transfers (PK/PD data, imaging data, Laboratory data) from external vendors and performs relevant review/reconciliation. Review query responses and ensure data quality. Reviews Site responses to queries and evaluates the necessity of a re-query. If applicable, communications with Site Coordinators are performed for resolution. Attends and may lead internal and external team meetings. Reviews and/or provides meeting minutes. Supports training and development of Clinical Data Coordinators. Assists with eCRF design. May be required to develop the eCRF and/or provide peer review. May serve as a back up to the LDM for internal and external study teams. N/A Education : Bachelor’s degree in related discipline and three years of related experience; or high school diploma and four years of related experience. Experience : See “Education.” Required Certifications : N/A Required Skills : Proficient with Microsoft Office Suite. Excellent written and oral communication skills. Excellent presentation skills. Strong organizational, problem-solving, and analytical skills. Ability to manage priorities and workflow. Versatility, flexibility, and a willingness to work within constantly changing priorities. Proven ability to handle multiple projects and meet deadlines. Strong interpersonal skills. Ability to deal effectively with a diversity of individuals at all organizational levels. Commitment to excellence and high standards. Creative, flexible, and innovative team player. Ability to work independently and as a member of various teams and committees. Good judgement with the ability to make timely and sound decisions. Ability to be discreet with sensitive company information.

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. Sr Associate IS Analyst What you will do Let’s do this. Let’s change the world. In this vital role you will be part of the Product Team responsible for completing the digital roadmap strategy, ongoing design, development, management, and optimization of Amgen Operation’s Electronic Lab Notebook (ELN) and Instrument Data Acquisition Platform. The ideal candidate will have an excellent grasp of the technology for Lab applications with a passion for fostering innovation and excellence in the biotechnology industry. Strong preference will be given to candidates with experience working in ELN Applications, Enterprise Application Integration, end-to-end data and process harmonization, as well as handling the seamless integration of Lab Instrument data to various enterprise business applications. This individual will also be engaging with key vendors and partners with collaborators orchestrating the implementation of solutions that enable next generation lab processes including simulations, machine learning and knowledge management. The ideal candidate will have a solid understanding of the end-to-end software development lifecycle, technical product ownership, business analysis, Scaled Agile framework, coupled with leadership and transformation experience. This role demands the ability to drive and deliver against key organizational critical initiatives, develop a collaborative environment, and deliver high-quality results in a matrixed organizational structure. Roles & Responsibilities: Develop and Maintain solutions for Operations Enterprise Lab Information Management solutions, including Biovia’s Holistic Lab ELN Platform. Support alignment of business processes with Holistic Lab ELN, Product Life Cycle Management (PLM), and Big Data technology capabilities by working with multi-functional representatives across Operations and sites. Develop and implement business process improvements to consistently enhance efficiency and effectiveness. Monitor, solve, and resolve issues related to case intake and case processing across multiple systems. Work closely with internal teams, external vendors, and business partners to address dependencies and resolve bottlenecks for critical issues Ownership in the development of test plans, scenarios to ensure robust validation of system updates, patches and new features Perform regression & functional testing to verify the changes do not negatively impact existing system functionality Work with other Amgen infrastructure teams to stand up various infrastructure environments (DEV/TEST/PROD) in the cloud or on-prem 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 with 5- 9 years of Life Science/Biotechnology/Pharmacology/Information Systems experience. Functional Skills: Must-Have Skills: Experience in user requirements and acceptance criteria in agile project management systems such as JIRA and identification and execution of scripts. Good communication skills and the ability to work with Product Managers and business collaborators to define scope and value for new developments Hands-on experience with the ITIL framework and methodologies like (Scrum). Knowledge of SDLC process, including requirements, design, testing, data analysis, change control Proven leadership skills with the ability to multitask and lead simultaneous software/hardware lifecycle projects Partner with vendors and other team members to troubleshoot problems, test new software versions, and secure long-term solutions for Platform roadmap Good-to-Have Skills: Hands-on experience in HP ALM, JIRA, Confluence, document management systems (e.g., CDOCs) and Service Now. Experience in management of test plans, test protocols, defect management, and requirements traceability matrix Experience of Continuous Integration and Continuous Delivery methodology Ability to work independently, excellent problem solving and professional written communications skills. Strong customer focus with ability to work closely with business collaborators to advance their organizational goals Experience working in a globally distributed enterprise application platform within the Lab solution landscape – including ELN, inventory management, MES and scientific analysis tools Worked in a highly regulated pharmaceutical or technology organization, with the ability to ensure compliance with industry regulations and standard methodologies for GxP software validation. Soft Skills: Excellent leadership and team management skills. Strong transformation and change management experience. Ability to work effectively with global, virtual teams. Excellent analytical and troubleshooting skills. Ability to manage multiple priorities successfully. Strong presentation and public speaking skills. Strong verbal and written communication skills. High degree of initiative and self-motivation. 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: The role is responsible for developing and maintaining the data architecture of the Enterprise Data Fabric. Data Architecture includes the activities required for data flow design, data modeling, physical data design, query performance optimization. The Data Modeler position is responsible for developing business information models by studying the business, our data, and the industry. This role involves creating data models to realize a connected data ecosystem that empowers consumers. The Data Modeler drives cross-functional data interoperability, enables efficient decision-making, and supports AI usage of Foundational Data. Roles & Responsibilities: Develop and maintain conceptual logical, and physical data models and to support business needs Contribute to and Enforce data standards, governance policies, and best practices Design and manage metadata structures to enhance information retrieval and usability Maintain comprehensive documentation of the architecture, including principles, standards, and models Evaluate and recommend technologies and tools that best fit the solution requirements Drive continuous improvement in the architecture by identifying opportunities for innovation and efficiency Basic Qualifications and Experience: Doctorate / Master’s / Bachelor’s degree with 8-12 years of experience in Computer Science, IT or related field Functional Skills: Must-Have Skills Data Modeling: Proficiency in creating conceptual, logical, and physical data models to represent information structures. Ability to interview and communicate with business Subject Matter experts to develop data models that are useful for their analysis needs. Metadata Management : Knowledge of metadata standards, taxonomies, and ontologies to ensure data consistency and quality. Hands on experience with big data technologies and platforms, such as Databricks, Apache Spark (PySpark, SparkSQL), performance tuning on big data processing Implementing Data testing and data quality strategies. Good-to-Have Skills: Experience with Graph technologies such as Stardog, Allegrograph, Marklogic Professional Certifications (please mention if the certification is preferred or mandatory for the role): Certifications in Databricks are desired Soft Skills: Excellent critical-thinking and problem-solving skills Strong communication and collaboration skills Demonstrated awareness of how to function in a team setting 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.

Job Title: Business Development Executive Company : St.Stone Medical Devices Private Limited Job Type : Full Time Schedule : Day Shift Timing : 10:00 AM to 6:00 PM Location: Onsite at A-80 DDA SHED, Okhla Phase II, Delhi Job Type: Full-Time Experience: 3-5 years of sales experience, preferably with a background in selling medical devices, equipment, or consumables to hospitals, clinics, diagnostic centers, or healthcare institutions. Job description * Promote and sell PICC lines, PD catheters, dialysis consumables, transfer sets, guidewires , and general disposable products to hospitals, clinics, and diagnostic centers. Build strong relationships with nephrologists, radiologists, intensivists, surgeons , purchase managers, and nursing staff. Identify new business opportunities and expand the customer base. Conduct product demonstrations, clinical training, and after-sales support. Regularly visit key accounts, track usage, and ensure product availability. Achieve and exceed monthly, quarterly, and annual sales targets. Coordinate with internal teams for order processing, deliveries, and issue resolution. Participate in trade shows, CMEs, exhibitions, and hospital events to promote the product line. Maintain accurate sales records, reporting, and forecasting. Qualifications & Requirements: Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or Business Administration. (Male Preferred). Minimum 3-5 years of experience in medical device sales , preferably in nephrology, radiology, or ICU disposables. Good knowledge of vascular access devices , catheter care, and dialysis-related products Strong communication, negotiation, and presentation skills Ability to work independently and travel extensively within the territory Proficient in MS Office and CRM tools Preferred Experience Previous experience selling to dialysis centers , radiology departments , or critical care units Understanding of hospital procurement processes and tender documentation Job Types: Full-time, Permanent Education: Bachelor's (Preferred) Experience: Business development: 3 years (Preferred) total work: 4 years (Preferred) Language: English (Preferred) Work Location: In person

The position is only for Science graduates, B. Tech or M. Sc. The candidate will be required to read and analyze patent documents including technical specifications, search and examination reports , prior art documents, non patent literature, decisions of Controllers of Patents and of Courts in Patent Infringement Cases. This will include analyzing prior art in relation to inventions and technologies and whether that reads on to the claims of a given patent. Candidate should have ability to draft and write or amend draft patent claims, analytical memos on statutory provisions pertaining to patents, draft responses to objections to grant of patent raised by patent examiners in examination reports, draft specification for patenting an invention or new technology, well-versed in interpretation of various provisions of Indian Patents Act, 1970 and Patent Rules 2003. EDUCATIONAL QUALIFICATION - B. Tech. in Electronics, Mechanical or Computer Sciences or M. Sc. in Chemistry or Biotechnology may apply Job Types: Full-time, Permanent, Fresher Pay: ₹18,000.00 - ₹40,000.00 per month Work Location: In person

Work Flexibility: Hybrid or Onsite What you will do � Complaint handling and Product investigations of medical devices Perform Visual, functional, dimensional, functional inspection & RCA of field returned products. � Maintain and ensure complaint files are complete and accurately reflect corresponding complaint activities. � Risk management –Risk assessment � Review of Process flow, DHR, Inspection plans, Measurement techniques, GRR’s etc. Review and analyze Literatures such as Clinical reports, PMCF reports, National register etc. to identify Complaints � Create PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis. � Other tasks as assigned by manager. What you need: Required skills: � B. Tech / M.Tech Mechanical, Biotechnology with 2-5 years of work experience. Hands on experience of PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis. � Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability. � 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. Preferred Skills: 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) Travel Percentage: None

JOB DESCRIPTION AND JOB SPECIFICATION FOR QUALITY CONTROL DESIGNATION – QUALITY CONTROL JOB TYPE – FULL TIME LOCATION – BHUBANESWAR SECTOR – FMCG COMPANY QUALIFICATION – DIPLOMA/B.SC/M.SC IN FOOD TECHNOLOGY/CHEMISTRY/BIOTECHNOLOGY/FOOD SCIENCE EXPERIENCED REQUIRED – 2-5 years Experience in Sauce, Pickle, Vegetable Preservation. Key Responsibilities: 1. Quality Inspections: Conduct regular inspections and quality tests on raw materials, in-process products, and finished products to verify compliance with standards. ( PHYSICAL INSPECTIONS: Chemical Inspections: Salt, Acidity, pH, TDS, Brix, Moisture, Ash, etc.) 2. Documentation: Maintain accurate records of all quality tests, inspections, and findings. Prepare reports summarizing test results. 3. Compliance Monitoring and Preparation of In-house Specification: Ensure adherence to food safety and regulatory requirements (e.g., FSSAI) throughout the production process. Monitor In-house RM, and FG as per specification and accepted after complying the same. 4. Problem Identification: Identify quality issues or deviations from standards and work with production teams to implement corrective actions. 5. Process Improvement: Collaborate with cross-functional teams to improve quality control procedures and processes. 6. Training: Train production staff on quality standards, and best practices to ensure consistent quality. 7. Audits : Participate in internal and external audits to assess compliance with quality standards and regulations. 8. Sampling and Testing: Collect samples for testing and conduct various laboratory tests (e.g., microbiological, chemical, physical) as needed. 9. Shelf Life Study: Conduct In-house Shelf Life study. 10. Chemical and Glassware Consumption: Oversee and record monthly/Daily Chemical and Glassware consumption, and order as per required. 11. Internal Calibration of Lab Equipment's: Conducting Internal Calibration of Lab equipment as per Internal Calibration Record. 12. Preparation of Lab Testing and Process SOP : Preparation of Lab testing SOP and process SOP. 13. Monitoring of Line Clearance and CIP: Monitoring of Line Clearance (Physical) and CIP (Physical and PH) 14. Keeping Counter Sample: Keeping sufficient counter sample of each batch of FG. 15. Calculation of Yield: Calculate RM requisition give to production team as per Final product batch and recipe. And record consumption of RM. CANDIDATE REQUIREMENTS We are looking for motivated and steadfast individuals who demonstrate: Proficiency in Quality testing methods and techniques. Understanding of food safety regulations and quality management systems. Strong analytical skills with attention to details. Ability to interpret technical documents and regulations. Excellent Communication and report writing skills. A disciplined approach to work and learning. The ability to work collaboratively in a team environment. Job Type: Full-time Benefits: Food provided Experience: total work: 2 years (Preferred) Work Location: In person

Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com. Job Description The Senior Clinical Data Coordinator (Sr. CDC) is a key member of the Development Operations, Data Management Team. The Senior Clinical Data Coordinator will provide data management support for all assigned studies. The Sr. CDC prepares, validates, processes, and maintains clinical data in support of submissions to international regulatory agencies or publication of manuscripts through the use of EDC and SAS software. Assist in the development of edit specifications, based on any available global medical standards, therapeutic area standards, and the protocol, used to clean the study. Performs user acceptance testing (UAT) on eCRF build and edit specifications. Creates supporting DM process documentation to LDM and/or performs peer review of documentation, including updating documentation. Support the coding schedule defined in the data management plan. Collaborate with data coding specialists on a regular basis to guarantee timely coding. Supports/maintains quarterly coding review cycles. Performs manual data listing reviews and submits queries as appropriate. Assist with and/or performs user acceptance testing of lab data standards. Evaluates quality of lab data entry and addresses inconsistencies with sites and CRAs as applicable. Assists in the SAE reconciliation process. This may include coordination with medical experts and Global Drug Safety. Follow up on discrepancies and resolve so both databases are consistent. Applies criteria for subject stage gate of No More Issues (NMI). Also, must coordinate and review medical and statistical queries and certify they are adequately resolved. Assist in the development of a blind review report and conducting a blind review meeting to assign patient validity. Assist in developing and generating study report listings according to ICH and if present company guidelines. Coordinate the query management system functions. Perform the final patient review and database lock activities. Assist in coordinating the processing of scheduled data transfers (PK/PD data, imaging data, Laboratory data) from external vendors and performs relevant review/reconciliation. Review query responses and ensure data quality. Reviews Site responses to queries and evaluates the necessity of a re-query. If applicable, communications with Site Coordinators are performed for resolution. Attends and may lead internal and external team meetings. Reviews and/or provides meeting minutes. Supports training and development of Clinical Data Coordinators. Assists with eCRF design. May be required to develop the eCRF and/or provide peer review. May serve as a back up to the LDM for internal and external study teams. N/A Education : Bachelor’s degree in related discipline and three years of related experience; or high school diploma and four years of related experience. Experience : See “Education.” Required Certifications : N/A Required Skills Proficient with Microsoft Office Suite. Excellent written and oral communication skills. Excellent presentation skills. Strong organizational, problem-solving, and analytical skills. Ability to manage priorities and workflow. Versatility, flexibility, and a willingness to work within constantly changing priorities. Proven ability to handle multiple projects and meet deadlines. Strong interpersonal skills. Ability to deal effectively with a diversity of individuals at all organizational levels. Commitment to excellence and high standards. Creative, flexible, and innovative team player. Ability to work independently and as a member of various teams and committees. Good judgement with the ability to make timely and sound decisions. Ability to be discreet with sensitive company information.

Ref Number B04-06341 Professional Expertise Research and Research Support Department UCL BEAMS (B04) Location UCL East Working Pattern Full time Salary £35,930-£41,255 Contract Type Fixed-term Working Type On site Available for Secondment No Closing Date 10-Aug-2025 About Us Surfactants, fragrances and polymers are key ingredients in Unilever’s household, laundry and personal care brands such as Persil, Comfort, Dove, and Sure. The EnzAct Prosperity Partnership, funded by BBSRC & EPSRC, aims to accelerate Unilever’s path to sustainability with enzymatic processes to create the next generation of surfactants, fragrances, and functional polymer ingredients for Unilever products. Currently, a significant proportion of ingredients are from fossil carbon-derived sources and Unilever has pledged to replace such ingredients as part of their ambitious sustainability goals. By harnessing enzymes, which are nature’s catalysts, EnzAct aims to re-design surfactants, polymers and fragrances using bio-based feedstocks. About The Role The role will focus on the technology support of enzyme processing and downstream purification. The primary objective will be to establish experimental data harvest from upstream and downstream processing at bench and large laboratory scale, speeding process development cycles through efficient data harvest. This is a multi-disciplinary project, integrating world-leading expertise in biotechnology, process development and sustainable manufacturing. This is an exciting opportunity to shape and create a cutting-edge sustainability platform, which will provide cost-effective and renewable processes to bring about resource circularity. The role will be funded for up to 18 months in the first instance. About You We are seeking a highly motivated biotechnology technical specialist to join the Prosperity Partnership team. You will have existing experience with speeding process development cycles through experimental data harvest from continuous enzyme, fermentation and adsorption processing. You’ll have the ability to generate, analyse and document experimental data though efficient project management and creative problem solving. An ability to collaborate within a multi-disciplinary team is essential. What we offer As well as the exciting opportunities this role presents, we also offer some great benefits some of which are below: 41 Days holiday (27 days annual leave 8 bank holiday and 6 closure days) Additional 5 days’ annual leave purchase scheme Defined benefit career average revalued earnings pension scheme (CARE) Cycle to work scheme and season ticket loan Immigration loan Relocation scheme for certain posts On-Site nursery On-site gym Enhanced maternity, paternity and adoption pay Employee assistance programme: Staff Support Service Discounted medical insurance Visit https://www.ucl.ac.uk/work-at-ucl/rewards-and-benefits to find out more. Our commitment to Equality, Diversity and Inclusion As London’s Global University, we know diversity fosters creativity and innovation, and we want our community to represent the diversity of the world’s talent. We are committed to equality of opportunity, to being fair and inclusive, and to being a place where we all belong. We therefore particularly encourage applications from candidates who are likely to be underrepresented in UCL’s workforce. These include people from Black, Asian and ethnic minority backgrounds; disabled people; LGBTQI+ people; and for our Grade 9 and 10 roles, women. Our department holds an Athena Swan Gold award in recognition of our commitment and demonstrable impact in advancing gender equality. You can read more about our commitment to Equality, Diversity, and Inclusion here: https://www.ucl.ac.uk/equality-diversity-inclusion/ Available documents Attached documents are available under links. Clicking a document link will initialize its download. download: Biotechnology Technical Specialist.docx

Job Overview Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and process expeditable adverse events to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business. Responsible to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost-effective manner. He/she will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual. Summary Of Responsibilities Assist in the processing of Expedited Safety Reports (ESRs), Periodic Safety Reports (PSRs) and submission, including but not limited to: Maintenance of adverse event tracking systems. Set-up and maintenance of project files, and central files for documentation. Assist with the reporting of ESRs and PSRs to clients, Regulatory Authorities, Ethics Committees, investigators and Fortrea project personnel, as required, within study specified timelines. Ensure all incoming Adverse Event (AE)/ Serious Adverse Event (SAE) reports are appropriately logged into the departmental tracking application and forwarded to the centralized mailbox. Assist with processing of the adverse events, including but not limited to: Data entry of safety data onto adverse event tracking systems. Write patient narratives and code adverse events accurately using MedDRA (for Marketed products, if applicable). Assist in the listedness assessment against appropriate label (for Marketed products, if applicable). Generate queries for its collection of missing or discrepant information in consultation with medical staff, if needed. Submission of expedited SAE reports to clients, Regulatory Authorities, Ethics Committees, investigators, 3rd party vendors, Partners and Fortrea project personnel, as required within the agreed timelines. Maintenance of adverse event tracking systems Assist with peer/quality review of processed reports and support with trends and actions as needed. Assist in the reconciliation of databases, as applicable. Assist in the maintenance of files regarding adverse event reporting requirements in all countries. Work within the Quality Management System framework, including but not limited to Standard Operating Procedure (SOP), departmental Work Instructions (WIs) etc. as appropriate. Prepare and support coordination of safety study files for archiving at completion of projects. Arrange and schedule internal and/or external meetings/teleconferences. Train and mentor, the PSS Assistants or peers in their day-to-day activities. Build and maintain good PSS relationships across functional units. Ensure compliance of operations with governing regulatory requirements and applicable study/project specific plans. Assume responsibility for quality of data processed. Provide administrative support to PSS personnel. All other duties as needed or assigned. Qualifications (Minimum Required) PharmD/Mpharm/Bpharm + 2 year of relevant experience.. Degree preferred to be in one or more of the following disciplines: Pharmacy, Nursing, Medical Sciences, Life Sciences, or related area. * Safety experience includes actual experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions. ** Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, working in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitoring, Regulatory Affairs, or Quality Assurance. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Speaking: English and local language. Writing/Reading: English and local language. Experience (Minimum Required) Good Team player and offer peer support as needed. Ability to set priorities and handle multiple tasks. Attention to detail. Good written and verbal communication skills. Logical and spelling skills, preferably with an aptitude for handling and proof-reading numerical data. Good keyboard skills, preferably with knowledge of MS office and Windows would be beneficial. Ability to operate standard office equipment. Physical Demands/Work Environment Office Environment . Learn more about our EEO & Accommodations request here.

Summary The senior International Program Regulatory Manager (Sr. IPRM) works under limited supervision of the International Program Regulatory Director to support the design and execution of optimal registration strategies and plans for the assigned portfolio in the assigned International countries. By partnering efficiently with International Program Regulatory Directors, global DU and International (INT) regulatory stakeholders, the Sr. IPRM supports optimal pipeline planning accounting for regional priorities and efficient use of regulatory paths for acceleration in assigned countries. They support the timely execution of registration plans by the relevant line functions and the resolution of high priority topics. The Sr. IPRM uses global, regional and country sources to maintain the relevant databases on country requirements, pipeline information and registration plans across all INT markets and to disseminate relevant information to INT stakeholders. Sr. IPRM supports and implements initiatives to enhance efficiency in ways of working and functional excellence. The Sr. IPRM is a member of the INT RA subteam and may act as deputy of the IPRD on global RA subteams. The Sr. IPRM may lead or contribute to regional cross-functional initiatives and committees. About The Role Key Responsibilities Drives the execution of registration plans as defined in the INT RA subteam and in partnership with the countries, regional roles and global LFs as applicable. Drives the design, up to date maintenance and execution of registration plans for all INT countries in alignment with RA INT and RA DU, including procurement of ancillary document for submission dossier, review of and contribution to responses to Health Authority (HA) questions, follow up on key milestone activities by relevant RA and LF stakeholders. Maintain up to date contact CO contact lists for programs and COs in scope. Supports the IPRD in partnering with DU RA roles to obtain, digest and communicate efficiently pipeline information to relevant stakeholders. Drives updates to the country requirements and registration plans are performed timely and the necessary quality. Sr. IPRM supports and implements initiatives to enhance efficiency in ways of working and functional excellence. Supports the IPRD in the design and execution of plans for Emerging Markets Brands and may interface with the Emerging Markets Brands Center of excellence for assigned projects. Supports the IPRD in designing and executing registration plans for products that target diseases which are predominantly prevalent in INT countries. Partners with GRSS&C LCM group on geographic expansion plans and execution for INT countries. Drives the dissemination of information to and education of global roles on INT country/regional requirements. Support the execution of or act as a region representative in functional or cross-functional initiatives, particularly those with potential impacts on INT RA resources or FTE allocations. May act as deputy of IPRD on assigned programs. Meets objectives as defined in registration plans for the countries and portfolio in scope. Proof of maintenance and communication of country requirements and registration plans for INT countries. Minimum Requirements Minimum of 6 years in Regulatory, product development, minimum of 1 year’s country, regional or global Regulatory Proven track record of HA negotiations, Ability to develop and communicate strategic vision Ability to work in cross-functional environment, Proven expertise in project management Highly committed and team oriented, Proven strong matrix leadership skills Proven track record of early recognition of potential regulatory issues, complex situations, sound risk assessment and overcoming hurdles Strong team player, Proven track record of successful risk assessment, Organizational awareness Ability to travel and represent the organization Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Desirable: Advanced degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Commitment To Diversity And Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Should have knowledge in Clinical Data Management Should have good knowledge in edit checks crf design SAE Reconcilation crf annotation Clinical Data Management Trained Candidates Only Eligible Required Candidate profile Strong understanding of clinical data management and E2b Guidelines Excellent clinical assessment and Communication Skills

Job Title: Purchase and Procurement Officer Location: [Bangalore Outskirts, Malur.] Company: Biovet Pvt. Ltd. Department: Supply Chain / Procurement Reports To: Supply Chain Manager / Operations Head About Biovet Pvt. Ltd.: Biovet Pvt. Ltd. is a pioneering biotechnology company specializing in the research, development, and manufacture of veterinary vaccines and biologicals. With a strong focus on innovation and quality, Biovet is committed to improving animal health and contributing to global food safety. Job Summary: We are seeking a detail-oriented and proactive Purchase and Procurement Officer to manage the sourcing and acquisition of materials, components, and services necessary for our manufacturing and R&D operations. The ideal candidate will ensure cost-effective purchasing, timely delivery, vendor development, and compliance with quality standards and regulatory guidelines. Key Responsibilities: Identify and evaluate suppliers, negotiate contracts, and maintain strong supplier relationships. Develop and execute purchasing strategies aligned with production and inventory needs. Prepare purchase orders and ensure timely delivery of materials and equipment. Monitor supplier performance to ensure compliance with contractual terms, delivery schedules, and quality requirements. Coordinate with R&D, production, QA/QC, and warehouse teams to ensure seamless material flow. Manage procurement documentation in accordance with company policies and regulatory standards. Conduct market research to stay updated on material costs and industry trends. Assist in cost reduction initiatives and procurement process optimization. Maintain accurate procurement records and prepare periodic procurement reports. Ensure compliance with ISO, GMP, and other relevant standards. Qualifications: Bachelor's degree in Supply Chain Management, Business Administration, Engineering, or related field. 2–4 years of experience in procurement or purchasing, Must have pharmaceutical, veterinary, or biotech sector experience. Knowledge of procurement best practices, contract management, and supplier evaluation. Familiarity with ERP systems (e.g., SAP, Oracle) and procurement software. Strong negotiation, analytical, and communication skills. Ability to work collaboratively in a fast-paced, regulated environment. Preferred Skills: Experience in sourcing raw materials for vaccine production or biotech manufacturing. Understanding of import/export procedures and regulatory compliance (DGFT, customs, etc.). Certification in supply chain (e.g., CPSM, CSCP) is a plus.

We are seeking dynamic and results-driven Techno-Commercial Sales Executives to join our growing Seasoning Division. This is an exciting opportunity for professionals who blend strong sales acumen with technical knowledge of food seasoning applications. 🔍 Role Overview You will act as a key link between our customers and internal teams—driving sales, providing technical support, and ensuring customized seasoning solutions that meet client needs and market demands. 🛠️ Key Responsibilities Build and manage B2B client relationships with food manufacturers, QSRs, and distributors Understand customer requirements and suggest appropriate seasoning solutions in collaboration with R&D Lead product trials, sampling, and technical presentations Meet and exceed sales targets in your assigned territory Coordinate with internal teams for smooth execution and customer satisfaction Monitor market trends and competitor activities Maintain sales reports, forecasts, and client documentation Represent the company at industry exhibitions and trade shows 🎓 Desired Profile Education: Bachelor's degree in Food Technology, Chemistry, Biotechnology, or Business MBA in Marketing is an added advantage Experience: 3–5 years of B2B Sales experience in the food ingredients, seasoning, spice, flavour, FMCG, or food processing industry ✅ Skills & Competencies Solid technical understanding of seasonings, flavours, and food applications Strong communication, negotiation, and interpersonal skills Proficiency in MS Office and CRM tools Willingness to travel extensively Customer-centric, adaptable, and innovative

We are looking for a highly motivated and detail-oriented individual to join our team as a Trainee in Documentation at Vijaya Diagnostic Centre Limited. The ideal candidate should have 0-2 years of experience. Roles and Responsibility Manage and maintain accurate records and documentation. Develop and implement effective documentation processes. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Prepare and review documents such as reports, letters, and other correspondence. Ensure timely submission of documents to relevant authorities. Maintain confidentiality and handle sensitive information with discretion. Job Requirements Strong understanding of biotechnology, pharmaceuticals, or clinical research industry. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced environment. Proficiency in Microsoft Office and other software applications. Strong analytical and problem-solving skills. Ability to learn quickly and adapt to new situations. Experience working with electronic health records systems is an added advantage.

Job Title: Business Development Executive Company : St.Stone Medical Devices Private Limited Job Type : Full Time Schedule : Day Shift Timing : 10:00 AM to 6:00 PM Location: Onsite at A-80 DDA SHED, Okhla Phase II, Delhi Job Type: Full-Time Experience: 3-5 years of sales experience, preferably with a background in selling medical devices, equipment, or consumables to hospitals, clinics, diagnostic centers, or healthcare institutions. Job description * Promote and sell PICC lines, PD catheters, dialysis consumables, transfer sets, guidewires , and general disposable products to hospitals, clinics, and diagnostic centers. Build strong relationships with nephrologists, radiologists, intensivists, surgeons , purchase managers, and nursing staff. Identify new business opportunities and expand the customer base. Conduct product demonstrations, clinical training, and after-sales support. Regularly visit key accounts, track usage, and ensure product availability. Achieve and exceed monthly, quarterly, and annual sales targets. Coordinate with internal teams for order processing, deliveries, and issue resolution. Participate in trade shows, CMEs, exhibitions, and hospital events to promote the product line. Maintain accurate sales records, reporting, and forecasting. Qualifications & Requirements: Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or Business Administration. (Male Preferred). Minimum 3-5 years of experience in medical device sales , preferably in nephrology, radiology, or ICU disposables. Good knowledge of vascular access devices , catheter care, and dialysis-related products Strong communication, negotiation, and presentation skills Ability to work independently and travel extensively within the territory Proficient in MS Office and CRM tools Preferred Experience Previous experience selling to dialysis centers , radiology departments , or critical care units Understanding of hospital procurement processes and tender documentation Job Types: Full-time, Permanent Education: Bachelor's (Preferred) Experience: Business development: 3 years (Preferred) total work: 4 years (Preferred) Language: English (Preferred) Work Location: In person

Assistant Professor – English Department Location: NH-79, Manivizhundhan South, Attur, Salem, Tamil Nadu - 636 121 Plus Max Pavendhar College of Arts & Science , managed by A Leading Multinational Organization – Plus Max Group of Companies, is seeking a passionate and dedicated Assistant Professor of English to join our Department of English. This is a great opportunity to contribute to our vision of academic excellence, research, and holistic student development. Job Description: The Botany Faculty will be responsible for delivering high-quality education in plant sciences, fostering a research-oriented learning environment, supporting students academically and personally, and contributing actively to the academic and social life of the college. Responsibilities: Teaching and Curriculum Development: Plan, prepare, and deliver lectures, practical’s, and tutorials in core and elective botany courses. Design and update curriculum in line with current scientific advancements and UGC guidelines. Prepare teaching materials, lab manuals, assessments, and evaluation tools. Integrate technology and modern pedagogies into teaching practices. Mentoring and Student Support: Provide academic guidance and career counselling to undergraduate/postgraduate students. Supervise student research projects, internships, and botanical field work. Identify students needing extra support and provide personalized mentoring. Research and Scholarship: Conduct independent and collaborative research in plant biology, ecology, taxonomy, biotechnology, or related fields. Publish scholarly articles in peer-reviewed journals and present at academic conferences. Seek research funding through grants and collaborate on interdisciplinary projects. Collaboration and Professional Development: Engage in departmental meetings, curriculum planning, and inter-disciplinary initiatives. Participate in faculty development programs, workshops, seminars, and training. Maintain professional growth by staying updated on developments in botanical sciences. College and Community Engagement: Contribute to institution-level committees and events. Organize botanical exhibitions, awareness drives, nature camps, or field visits. Participate in outreach programs and collaborate with local institutions or communities. Qualifications: PG with Ph.D. / SET/NET/M.Phil qualification is mandatory. 3 to 5 years of teaching experience at the undergraduate level. Strong passion for teaching and mentoring students. Candidates with a strong commitment to excellence in botanical sciences, teaching, and research. Effective communication and interpersonal skills. Ability to foster an inclusive and engaging learning environment. Research potential with a commitment to scholarly contributions. Previous teaching experience at the Post graduate level is preferred. Note: Salary will be based on qualifications and experience and will not be a limiting factor for the right candidate. If you are passionate about inspiring future botanists and advancing the frontiers of plant science, we invite you to apply and be part of our dynamic academic community! Job Types: Full-time, Permanent Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

About Improzo At Improzo ( Improve + Zoe; meaning Life in Greek ), we believe in improving life by empowering our customers. Founded by seasoned Industry leaders, we are laser focused on delivering quality-led commercial analytical solutions to our clients. Our dedicated team of experts in commercial data, technology, and operations has been evolving and learning together since our inception. Here, you won't find yourself confined to a cubicle; instead, you'll be navigating open waters, collaborating with brilliant minds to shape the future. You will work with leading Life Sciences clients, seasoned leaders and carefully chosen peers like you! People are at the heart of our success, so we have defined our CARE values framework with a lot of effort, and we use it as our guiding light in everything we do. We CARE! Customer-Centric: Client success is our success. Prioritize customer needs and outcomes in every action. Adaptive: Agile and Innovative, with a growth mindset. Pursue bold and disruptive avenues that push the boundaries of possibilities. Respect: Deep respect for our clients & colleagues. Foster a culture of collaboration and act with honesty, transparency, and ethical responsibility. Execution: Laser focused on quality-led execution; we deliver! Strive for the highest quality in our services, solutions, and customer experiences. About The Role The Consultant - Forecasting is responsible for developing, delivering, and maintaining forecasts (patient-based, TRx-based, etc.) and business insights for Improzo’s clients. The Consultant will work with clients in forecasting, market research, market access and other cross-functional teams. The position involves managing client relationships and directly interacting with and presenting to client stakeholders. You will need to leverage your quantitative and qualitative skills to not only create and analyze number-driven models, but creatively develop methods/approaches and deliver the story as well – this needs to be accomplished through a combination of analyzing client-provided data and secondary desk research. Experience with IQVIA or Symphony data (e.g., Xponent, DDD) is required. Working knowledge of patient-level data is a plus. Key Responsibilities Project Management: Play an integral role in executing analytics/consulting engagements through effective and efficient project management. Generate forecasts, analysis and actionable insights that lead to the achievement of strategic and financial goals for our clients. Manage and coordinate complex consulting engagements through strong client and people management, subject matter expertise, communication skills (both written and verbal), and the ability to draw conclusions and recommendations from a variety of evidence. Operate effectively as part of a global team, by participating and contributing to client discussions and proactively helping them with their decisions in creating and/or validating assumptions. Provide robust competitive assessments and insights that inform key decision-making processes for clients such as strategic brand planning, forecasting, and lifecycle management. Perform in-depth (secondary) market research and data analysis to derive understanding of the disease and patient segments based on client requirements. Analyse and integrate primary research and secondary data with other market knowledge to draw inferences and conclusions. Identify risks and opportunities for the business and support key decisions on business strategy with customer and market insights. Leverage all relevant data such as DRG/IQVIA to provide insights into forecast assumptions. Forge effective relationships with various stakeholders (both internal and external), e.g., teams running Market Research initiatives. Ensure effective delivery of work (models and presentations) to clients onsite or through video/teleconferences, through self and others in accordance with the project timelines and quality parameters. Convert Excel models into presentable reports and PowerPoint slides for effective utilization by clients, focusing on the storyboarding and narrative. Leadership Will be responsible for overall leadership, talent development, skill advancement, and engagement and retention of talent in the team (in case acting in the capacity of a team lead). Foster learning mindset in the team to proactively develop research and story-telling skills, leveraging multiple sources of data to answer business questions. Develop new capabilities leveraging new sources of data and methods that include segment-level analysis, etc. Engage with internal and external stakeholders to build effective relationships to create win-win engagement models. Mentor/Guide team members who can benefit from your expertise and experience. Qualifications Bachelors/Masters in Pharma / other life sciences background (Biotechnology, Bioinformatics, etc.) or bachelor’s in engineering / B. Tech or Master’s in Business Administration. 3-4 years of relevant forecasting and commercial analytics experience. Experience building financial models (e.g., market sizing, sales, and profit forecasts) using Microsoft Excel and other tools. In-depth expertise in developing, implementing, and managing holistic strategies for modelling (design, development, validation, calibration, documentation, approval, implementation, monitoring and reporting) in collaboration with life sciences teams. Broad experience in key functional areas of CI, analytics, and market research including the ability to understand and identify key business levers. Strong strategic skills including ability to see the big picture, along with conceptual and out-of-the-box thinking. Work experience in the US/European pharma industry is a plus. Ability to balance conflicting priorities. Proven people management skills. Other Competencies Entrepreneurial orientation. Excellent interpersonal and communication skills (written and verbal). Innovative and collaborative behavior, team player. Customer centricity and paying attention to details. Benefits Competitive salary and benefits package. Opportunity to work on cutting-edge tech projects, transforming the life sciences industry Collaborative and supportive work environment. Opportunities for professional development and growth. Skills: skills,life sciences,data analysis,client relationship management,management,customer,excel,iqvia data,powerpoint,market access,forecasting,project management,research,market research,data

Job Title - GN - SONG - MT - LifeSciences - Associate Director Management Level: 05/ Associate Director Location: Gurugram, Mumbai, Pune, Bengaluru, Hyderabad, Chennai Must have skills: Life Sciences Good to have skills: Digital Marketing Job Summary: The Life Sciences Marketing Senior Manager position is within the Marketing Transformation vertical of Accenture GN Song. The individual would work at the heart of the top global Life Sciences (Pharmaceuticals, Biotechnology and Medical Technology) and would collaborate on innovative projects while bringing in deep industry knowledge and Marketing skills. Areas of Work: Digital Marketing, Creative Strategy, Brand Strategy, Campaign Management, Next Best Action Marketing, Mar-Tech Strategy, Customer Experience & Journey Development. Roles & Responsibilities: Strong project management skills to plan, execute, and deliver content initiatives successfully. This includes managing timelines, budgets, resources, and coordinating cross-functional teams. An analytical & data driven mindset to drive result-oriented decisions Exposure and experience in roles across the marketing value chain, primarily in the life sciences or allied industries as detailed out below. Consulting & Advisory service Market Research Analysis and assessment of the pharmaceutical market across disease areas and opportunity identification for new launches, indication expansions, identify emerging trends, competitive landscapes, and new opportunities within the life sciences sector. Competitor benchmarking, patient journey mapping, segmentation & targeting Digital Marketing Develop E2E strategy & campaigns: Liaise with key client stakeholders in the marketing teams to design strategies for omni-channel marketing campaigns. Lead development of content marketing, social media, and web engagement programs for the client, ensuring that they are aligned with the overall content strategy. In-depth knowledge of branding, creative development and execution, digital marketing, and campaign deployment and optimization Provide expertise on Content design and campaign execution: Able to provide a perspective on identification and selection of the right digital channels and content types based on campaign objectives. Able to understand client requirements based on their briefs & ideate to appropriate creative designs. Support end to end campaign execution and suggest ways for optimization. Marketing Technology Lead platform assessment and solution design : Understand the marketing value chain across process, technology & people. Conduct a thorough assessment, propose a solution along with an operating model & define KPIs for different marketing technologies – Adobe / SF / Veeva. Have an understanding of the regulatory, compliance and governance landscape in the industry and build frameworks for scale up. MarTech Consulting Projects: Lead projects focusing on optimizing the MarTech stack and develop use cases to improve utilization of existing MarTech stack. Research, evaluate and recommend new martech systems and suppliers. Keep a holistic understanding of existing and upcoming martech platforms and how they connect into the broader marketing technology landscape. Tools & Platforms: Hands on experience on Mar-tech tools such as Adobe campaign, Marketo, Adobe, Cloud, Google Marketing platform, Google Ads, Pega decisioning, SFMC etc. Value realization : Crafting a value tree and developing business cases for implementation and scale up Gen AI Be aware of the latest AI developments in the Life Science industry and be able to co-create customized solutions for the client to meet their objectives. Have experience in CDP tools and platforms. Design and implement GenAI use cases Sales & Business Development Generating new business engagements: Drive new business opportunities by identifying and pursuing new leads, defining GTM strategy, facilitate client discussions and presentations to drive new business and client relationships. Own and drive RFP/RFI response coming in from Life Science customers Practice Development Take on leadership role: Support overall growth of practice across all the pillars – Marketing as well as sales, & service through a combination of business development, talent management, oversight of delivery work, and thought leadership. Collaborate with Salesforce, Veeva, Adobe, IQVIA etc. business groups, to enable business capabilities with agility, velocity, and quality while optimizing costs. Establish a strong network with key stakeholders in the Accenture ecosystem, across geographies to socialize and amplify the GN Song capabilities, operating model and ways of working to generate demand and meet the KPIs Lead and motivate teams with diverse skills and backgrounds. Manage and mentor talented teams of consultants and technologists supporting, providing input and guidance into the talent strategy and actively participate in engagement, capability development activities. Professional & Technical Skills: In-depth knowledge of branding, creative development and execution, digital marketing, and campaign deployment and optimization Experience in working with middle to senior management levels within existing organization / client organizations Experience in working with Agencies or working in a Marketing agency for Life Sciences Clients Strong understanding of marketing, advertising technologies (with hands on) and ability to apply technology know-how to better how our clients reach out to their customers Additional Information: MBA from a tier 1 institute with preferably bachelor’s degree in marketing, Journalism, Communications, or a related field Proven working experience (8+ years) in digital marketing/Advertising platforms and in delivering marketing solutions, particularly within the Life Sciences Industry About Accenture: Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions — underpinned by the world’s largest delivery network — Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With 624,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at About Our Company | Accenture About Accenture Strategy & Consulting: Accenture Strategy shapes our clients’ future, combining deep business insight with the understanding of how technology will impact industry and business models. Our focus on issues such as digital disruption, redefining competitiveness, operating and business models as well as the workforce of the future helps our clients find future value and growth in a digital world. Today, digital is changing the way organizations engage with their employees, business partners, customers, and communities. This is our unique differentiator. To bring this global perspective to our clients, Accenture Strategy's services include those provided by our Global Network – a distributed management consulting organization that provides management consulting and strategy expertise across the client lifecycle. Our Global Network teams complement our in-country teams to deliver cutting-edge expertise and measurable value to clients all around the world. For more information visit https://www.accenture.com/us-en/Careers/capability-network Accenture Global Network | Accenture in One Word At the heart of every great change is a great human. If you have ideas, ingenuity and a passion for making a difference, come and be a part of our team. , Experience: Minimum 15+ year(s) of experience is required Educational Qualification: MBA/PGDM from a tier 1 or 2

Internship Summary: We are seeking a motivated and detail-oriented Product Specialist Intern to join our team. This role provides a unique opportunity to gain hands-on experience in the medical device industry, working closely with R&D and other departments. As an intern, you will assist in product development, market research, and client support activities, helping to ensure our devices meet the highest standards in clinical application and user satisfaction. Key Responsibilities: Support R&D team in developing and refining medical devices. Assist in product testing, usability studies, and gathering feedback from healthcare professionals. Help prepare product documentation, including technical specifications, training materials, and user manuals. Assist with troubleshooting and resolving customer inquiries related to product functionality and usage. Qualifications: Currently enrolled in a Bachelor’s or Master’s program in Biomedical Engineering, Biotechnology or a related field. Strong interest in medical devices and healthcare technology. Excellent research, analytical, and problem-solving skills. Strong verbal and written communication skills . Ability to work collaboratively in a team environment and manage multiple projects. Basic knowledge of medical terminology and regulatory standards is a plus. What We Offer: Hands-on experience with cutting-edge medical device technology. Mentorship and guidance from experienced product specialists and R&D professionals. Opportunity to contribute to real-world projects that impact patient care. Networking opportunities and career development resources. Stipend: This internship offers a monthly stipend of ₹10,000 for the duration of the 3-month period with potential for full-time employment based on performance No .* Of Opening: 2* Who can apply? Recent graduates from the 2025 batch who are interested in building a career in healthcare technology. Send your resume to : hrm@vrpmedgands.com/9597123526 Job Type: Full-time Pay: Up to ₹10,000.00 per month Benefits: Commuter assistance Flexible schedule Leave encashment Paid sick time Paid time off Application Question(s): Are you comfortable to travel within cochin, kerala? Education: Bachelor's (Preferred) Language: English (Required) Willingness to travel: 50% (Preferred) Work Location: In person Expected Start Date: 23/07/2025

Senior Drug Safety Associate Category: Reg Affairs & Safety Pharmacovigilance Location: Bangalore, Karnataka, IN Novo Nordisk Global Business Services Senior Drug Safety Associate Are you driven by challenges and energized by a fast-paced, dynamic environment? Do you thrive in a role where strategic alignment, stakeholder collaboration, and continuous improvement are key to success? We are looking for a Senior Drug Safety Associate to join our growing team in an international setting. In this pivotal role, you will work closely with cross-functional teams to ensure the highest standards of patient safety and regulatory compliance throughout the drug development lifecycle. Apply now and become part of a collaborative, forward-thinking environment where your expertise truly makes an impact. About The Department: Global Patient Safety Bangalore (GPS-BLR) was set up in 2010 as one of the hubs for safety case processing. We handle case processing and medical review of Individual Case Safety Reports from different sources (spontaneous, literature, solicited and clinical trials). We are additionally engaged in safety surveillance, safety medical writing, safety report submission, training, quality control of ICSRs, Argus configuration and maintenance, information technology quality assurance, training co-ordination and literature surveillance activities, including medical literature monitoring. The Position : As a Senior Drug Safety Associate you will be responsible for the comprehensive management of both serious and non-serious adverse event reports from various sources. Your core duties will include initial medical evaluation, accurate case entry, and verification of safety data within the Novo Nordisk safety database (Argus). You will ensure consistent and precise coding using MedDRA, evaluate causality, seriousness, and listedness, and ensure that case narratives reflect accurate and relevant safety information. You will also assess the need for follow-up, issue appropriate queries in the EDC system and/or to affiliates, and actively participate in weekly literature surveillance activities. Responsible to conduct medical evaluation, coding, and case processing of serious and non-serious adverse events in compliance with GxP and regulatory requirements, using Argus and MedDRA. Liaise with global affiliates, partners, and internal stakeholders to clarify safety data, ensure timely follow-up, manage local literature, and support compliance activities. Collaborate with Safety Reporting and IT teams for data retrieval, custom reporting, and to assess system/process changes impacting pharmacovigilance operations. Ensure Support system optimization and data integrity, collaborating with Safety Reporting and IT for custom data retrieval, reporting, and assessing the impact of system or process changes on pharmacovigilance activities. Mentor and train colleagues, act as a buddy, and proactively contribute to continuous process improvement across global safety functions. Qualifications: We are looking for a candidate who can bring the following skills and experience to the role: Graduation and/or post-graduation in Life Sciences (e.g., Medicine, Pharmacy, Biotechnology, Nursing). Minimum experience of 4 years in processing of Individual case safety reports (ICSR). Experience in mentoring, training, quality trend analysis will be preferred. Sound knowledge and hands-on experience in Pharmacovigilance and adverse event reporting processes which includes triage/intake, data entry, Quality review within various case types. Knowledge of safety databases like Argus and familiarity with MedDRA coding. Strong understanding of medical terminology, clinical pharmacology, and global PV regulatory requirements. Familiarity with GxP as well as GDPR standards and compliance expectations within a pharmaceutical setting. Proficient in MS Windows applications, including Excel, Word, Outlook, and PowerPoint. Excellent written and verbal communication skills in English, with a strong ability to convey medical and scientific concepts clearly. Proven ability to work within cross-functional teams and collaborate across global departments and affiliates. Demonstrated ability to foresee and assess the impact of system/process changes on safety operations. Solid understanding of Novo Nordisk products, including mechanisms of action, safety profiles, and patient populations. Experience working in a pharmaceutical company or a similar organization. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 72,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact To submit your application, please upload your CV online (click on Apply and follow the instructions). Deadline 29th July 2025. Disclaimer It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.

At Ecospice Ingredients Pvt. Ltd., specializing in the production and export of high-quality essential oils, oleoresins, and spice extracts, derived from nature's finest botanicals. Our advanced manufacturing facility, nestled in the heart of Kerala's spice-growing region, is situated within our own spice plantation in Idukki, ensuring freshness, traceability, and quality from farm to formula. With a strong emphasis on purity, innovation, and sustainability, we cater to various industries including food & beverage, pharmaceuticals, cosmetics, perfumery, and wellness. Our cutting-edge extraction techniques preserve the full flavor, aroma, and therapeutic value of each ingredient. Ecospice Ingredients Private Limited is hiring for the position of Assistant Manager - NPD & R&D in Vadavucode, Ernakulam, Kerala. The ideal candidate should have a minimum of 5+ years of experience in the essential oils, oleoresins, nutraceuticals, or natural extracts industry, along with technical expertise and team leadership skills. As the Assistant Manager - NPD & R&D, you will be responsible for leading and managing the NPD & R&D team to develop new formulations and product innovations aligned with company objectives. You will coordinate with various departments for seamless NPD execution, conduct feasibility studies, ensure compliance with regulatory requirements, and lead troubleshooting efforts while providing technical support to sales and customer service teams. Qualifications required for this role include a B.Tech / M.Tech / M.Sc in Food Technology, Biotechnology, Chemistry, or related disciplines, along with a strong understanding of extraction techniques, emulsification, and product stability. Key attributes such as leadership, analytical thinking, communication skills, and a passion for innovation in natural products are essential for this position. If you are ready to drive innovation at a rapidly growing natural ingredients company and possess the required qualifications and attributes, we encourage you to apply for this exciting opportunity at Ecospice Ingredients Private Limited.,