1074 Glp Jobs - Page 17

Role Overview: As a Chemist in the Instrumentation Laboratory (Residue Lab), you will be responsible for the preparation and analysis of samples using various Instrument techniques while ensuring strict adherence to safety and documentation protocols. Your role will involve receiving, handling, and storing samples and standards, conducting analysis on instruments in compliance with regulations, and contributing to method development and validation. Strong analytical skills and knowledge of NABL and ISO/IEC 17025:2017 standards are essential for this role. Key Responsibilities: - Sample Preparation & Analysis: - Receive, handle, and store samples - Prepare samples, conduct analysis, and gener...

Computer System Validation (CSV) Professional Join Sartorius as a Senior Computer System Validation (CSV) Professional and become a key player in driving harmonization, compliance, and quality assurance within our Confidence Validation Services Quality team. In this impactful role, you will lead the establishment of a harmonized validation policy, ensuring our computer systems are compliant with the latest regulatory standards (e.g., 21 CFR Part 11, OECD 17, OECD 17 supplement 1, EU-GMP Annex 11). Your expertise will be instrumental in implementing state-of-the-art tools such as an eQMS and ELN/LIMS, enhancing our service departments efficiency and quality. Additionally, you will have a chan...

Officer Quality Control - API & Intermediates Education - M.SC - Analytical / Organic Experience 1 to 3 years experience in Quality Control from pharmaceutical industry. (This is a Fixed Term Contract role - On Company's Contract) Job Description - Sampling of raw, packing material, intermediate & finished product. Analysis of raw, packing material, intermediate, stability samples & finished product. Analysis of process & cleaning validation samples. Preparation of standard volumetric solution, reagent & standardization of volumetric solution and check for stability. Inventory of Instruments Spares, Chemicals & Glassware. To maintain cleanliness, personal and environmental safety & follow Go...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Job Title Officer, QC Micro Business Unit Global Quality Compliance Job Grade G12B Location : Sikkim, Unit II At Sun Pharma, we commit to helping you ?Create your own sunshine?? by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community, Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, youll find yourself becoming ?Better every daythrough continuous progress Exhibit self-drive as you ?Take chargeand lead with confidence Additionally, demonstrate a collaborative spirit, knowing that we ?Thrive togetherand support each others journeys ? Key Responsibilities No Responsibilities 1 Sampling, analysis and r...

Conduct chemical synthesis of new and existing agrochemical compounds in the lab. Develop and optimize synthetic routes and reaction conditions to improve yield, purity, and cost-effectiveness.

Analytical method development Analytical method validation Stability studies Extractable and leachable Standards generation Calibration of Instruments All related works as per USFDA and NABL norms

B.Sc/M.Sc Chemistry, 1–8 yrs exp in API/Pharma QC. Must handle HPLC/GC/UV/IR, cGMP, stability, and docs. Local preferred Dahej. Only male candidates are required. Only pharma experience required.

As a Research Associate/ Executive/ Analyst at Syngene International Ltd., you will be a part of the Small Molecule Bioanalytical Laboratory in Bangalore, India. Reporting to the Project Leader / Group Leader, your role will involve conducting BA/BE studies, method development, and validation programs, ensuring technical and regulatory compliance. Key Responsibilities: - Perform bioanalytical work including sample processing, method development, validation, and study sample analysis in compliance with SOPs and STPs. - Prepare STP, MV protocol, and study sample analysis protocol. - Coordinate with the maintenance department for equipment failures. - Document data entries and ensure regulatory...

As a Masters graduate from 2024 to 2025 in the locations of Walajabad, Sunguvarchathram, Sriperumbudhur, Kanchipuram, you will be responsible for the following: - **Testing and Analysis:** - Perform analytical testing on raw materials, in-process samples, and finished products using techniques such as HPLC, UV, pH Meter, and etc. - **Documentation:** - Accurately document test results and observations following Good Documentation Practices (GDP) for audit readiness. - Prepare specifications for raw materials, packing materials, finished products, intermediates, solvents, and reagents used in analyses. - Inspect, sample, and test starting materials, packaging materials, semifinished, and fini...

Preparation of study plan considering the client requirements as well as regulatory requirements. Preparing a study schedule and communicating with all the study personnel and ensuring the proper conduct of the study. Preparing reports after completion of each study. This involves evaluating the data output by applying scientific knowledge and skills. To maintain the highest regulatory standards (OECD GLP) during any activity conducted in the facility by continuous monitoring and checkup of all the instruments/equipment used in a study as per Standard Operating Procedures (SOPs). Preparation and periodic revision of Standard Operating Procedures. Preparation and presentation of experiment co...

Oversee the implementation, maintenance, and continuous improvement of GLP systems and processes. Investigate and resolve any GLP-related deviations, non-conformances, or audit findings. Develop and maintain SOPs related to GLP compliance.

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and ...

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and ...

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and ...

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and ...

Job description Bangalore, India Job category Commercial Marketing Department Commercial, GBS Are you passionate about taking your competitive intelligence journey to next level Do you want to work for a globally renowned organization Novo Nordisk We are seeking a Global Competitive Intelligence Associate Lead to join our vibrant and fast-moving Commercial-GBS team in Bangalore, India. If that sounds like you, read on and apply today for a life-changing career. The position As a Global Competitive Intelligence Associate Lead at Novo Nordisk, you will be responsible for: Consistently track and monitor activities of pharmaceutical competitors and man-aging news on competitors from key scientif...

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

ensure compliance with cGMP, cGLP, SOPs & regulatory norms. Prepare/review QMS docs (SOPs, CAPA, Deviation, OOS, Complaints). Oversee production, resource planning, validations, in-process checks & documentation (BMR/BPR). Coordinate with QA/QC/

Role & responsibilities : As a Quality Control Associate, you will be responsible for ensuring that products or services meet established quality standards and comply with industry regulations. Your main tasks will include conducting inspections, tests, and analyses at various stages of the production process. You will collaborate closely with production teams to identify and address defects, deviations, and quality issues. Preferred candidate profile Preferably one who handles the HPLC method and is near to doddaballpur not from the Pharma industry preferably from agri, chemist, soil background and they have taken full responsibility of QC and QA and knowledge.

Key Responsibilities: 1. GxP Compliance: Lead the validation team in ensuring all processes adhere to GxP standards, including GLP, GCP, and GMP, and maintain compliance with regulatory requirements 2. Validation Strategy: Develop and implement validation strategies, including risk-based approaches, to ensure systems and processes meet regulatory and industry standards 3. Team Management: Supervise and mentor validation engineers/specialists, providing guidance on GxP, validation testing, and CSV best practices. 4. Computer System Validation (CSV): Oversee the development, review, and approval of CSV documentation, including validation plans, protocols, reports, and risk assessments. 5. Prod...

As a seasoned professional in the field of pharmaceutical sciences, you will be responsible for providing technical expertise, strategic leadership, project management, regulatory compliance, and team development in the realm of liposomal drug products. Your primary focus will be on guiding formulation design, optimizing processes, and ensuring adherence to global regulatory requirements for liposomal generics. Utilizing a science-driven approach, you will tackle complex challenges in formulation and manufacturing to drive project success. Leading and managing R&D projects centered on liposomal formulations will be a key aspect of your role, aligning these initiatives with organizational goa...

Date: 2 Sept 2025 Location: Bangalore, KA, IN, 560100 Custom Field 1: Discovery Services Job Description Role: Bioanalytical Manager, Immunogenicity Research Laboratory Job Location: Bangalore, India Reporting to: HOD of Large Molecule Bioanalytical Laboratory The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngenes 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturin...

Walk In Interview at Vapi. Date : 14-09-2025 (Sunday) Designation: QC Officer-Sr. Officer Job Location: Daman Qualification: M.Sc (Chemistry). / B. Pharm/ M. Pharm Experience: 02 to 07 Years (OSD) Required Candidate profile Roles and Responsibilities: -Analytical Validation -Finished Goods -Stability -Raw material -GLP -(HPLC user must)

To check and monitor the GMP and GLP compliances. Dispatch of goods from plant - completion of all documentation and give the batch release To be responsible for overall quality assurance functions in the factory. To approve and monitor all SOPs related to QA, QC, Production, stores, Admin and Engineering departments. To approve all specifications of Raw Materials, Packing Materials, Intermediates and Finished Goods. To review and approve Validation Master Plan, Master Formula Records, Master BMR, Master BPR, Site master files. To approve and monitor all process validations, Cleaning validations, Hold Time Studies, Validations of premises, equipment and procedures. To approve the stability p...