1074 Glp Jobs - Page 8

As a Senior Executive QC in the Pharma and Herbal industry, you will be responsible for managing the QC laboratory and ensuring compliance with cGMP and GLP requirements. Your role will involve supervising QC analysts to maintain seamless laboratory operations and overseeing the testing of incoming raw materials, bulk, semi-finished, and finished products. You must have a minimum of 5-8 years of experience and demonstrate proficiency in operating HPLC, GC, UV, and other instruments used in QC analysis. Key Responsibilities: - Manage the QC laboratory in compliance with cGMP and GLP requirements - Supervise QC analysts to ensure seamless laboratory operations - Oversee regular testing of inco...

Role & responsibilities Job Title: Quality Control / Quality Assurance Executive (Fresher) Industry: Pharmaceuticals Manufacturing Department: Quality Control (QC) / Quality Assurance (QA) Company: Vivek Pharmaceuticals Pvt Ltd Location: Jammu Employment Type: Full Time Experience: 0 2 Years Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry, Microbiology, Biotechnology or related field) Job Summary: We are looking for passionate and detail-oriented candidates to join our Quality team. The selected candidates will be part of controlling product quality, compliance with regulatory requirements, and in all quality operations. Key Responsibilities: Quality Control (QC): Conduct routine t...

Role & responsibilities Complete Analysis of various raw materials, In-process, Drug substance and finished Products in line with Pharmacopeia method and in-house Specification and test procedures. Change Control, Deviation, Root Cause investigation, CAPA, OOS, OOT, Incidence Calibration of Instruments HPLC , UV-Visible Spectrophotometer, pH Meter,KF Titrator, weight balance. Working standard preparation as per SOP. Ensure the timely analysis of samples GLP, GMP, GDocP (With respect to Regulatory Guidelines) Function in details of various Section of QC/QA(Eg.Raw Material, Finished Product,Stability Study etc. Data Integrity 21 CFR Part 11 Qualification, Calibration, Validation. Maintaining t...

As a Quality Control Analyst at Roquette, your role involves managing, developing, and optimizing customer satisfaction through stringent monitoring of quality parameters. You will be responsible for enabling HACCP study and involving in RCA whenever there is any process deviation. Reporting to the QC Manager and working as part of the QC team, you will support overall site QC activities. Key Responsibilities: - Analyzing the production batches. - Maintaining GLP data. - Reporting in Excel sheets daily. - Conducting ERP data for QC. - Performing party sample analysis & reporting. - Training packing & loading casuals about food safety. - Facing audits and responding to customer complaints. - ...

As a Quality Control & Microbiology Department Manager, your role involves ensuring online documentation compliance with cGMP & GLP standards. You will be responsible for overseeing testing procedures, reviewing specifications, and approving necessary documentation. Your key responsibilities include: - Ensuring all testing is conducted according to approved specifications and standard procedures - Reviewing and approving specifications and test procedures for starting materials, in-process, and finished products - Checking and approving certificates of analysis for raw materials, in-process samples, packing materials, and finished products - Supervising online data recording during analytica...

Reporting to the Analytical Head. Implementing quality management systems per USFDA, MHRA, WHO, Compliance of 21CFR, ISO/IEC 17025, and other Regulatory Requirements for GLP. Ensuring the availability of reference materials/working standards. Training, qualifying, and assigning tasks to staff. Ensuring smooth operations of equipment/instruments. Signing reports and verifying external calibration certificates. Supervising technical staff and managing change control, deviation control, OOS, and CAPA. Approving specifications, sampling instructions, test methods, and other Quality Control procedures & records.

,in-processthe ,for leading,for leading,problem-solvingResponsibilities We are looking for a senior professional AGM with a range of 15 to 20 years of experience in Analytical Method Validation for regulated markets. The role involves leading API and excipient method validation across multiple dosage forms and managing a team of 30, including three senior managers. The ideal candidate must be technically strong, experienced in US/EU compliance, and hold an M. Pharm, M.Sc., or Ph.D. Role & responsibilities: Accountable to lead the team for AMV of OSD, Nasal, Injectables, Ophthalmic and Topical dosage formulations. Responsible for RM & PM characterization and documentation. Generate qualificat...

Eligibility Criteria Work Experience: Minimum 1 year (QA / QC in Manufacturing preferred) Qualification: M.Sc. / B.Sc. (Chemistry) Age: Up to 26 years Gender: Open (Any) Language Preference: English Hindi (good in English) Industry Preference: Manufacturing / Chemicals / Pharma Key Responsibilities Ensure compliance with QA standards, SOPs, and regulatory guidelines . Conduct sampling, testing, and analysis of raw materials, in-process, and finished products. Prepare and maintain QA documentation, reports, and audit records . Perform in-process quality checks to ensure production consistency. Coordinate with Production, QC, RD, and Supply Chain for quality-related activities. Support impleme...

As a Head Quality Control at Fishfa Biogenics, you will be responsible for overseeing the quality control operations within the company. You should have 8-12 years of experience in Biological API, Testing, QMS, and GLP. Key Responsibilities: - Manage and lead the Quality Control department, ensuring compliance with regulatory standards and company policies - Develop and implement quality control procedures for Biological API, Testing, QMS, and GLP - Conduct quality audits and inspections to identify areas for improvement and ensure quality standards are met - Collaborate with other departments to address quality control issues and drive continuous improvement initiatives - Train and mentor q...

Role & responsibilities Key Responsibilities Execution of experiments: Conduct experiments to evaluate water purifier-based components such as sediment, carbon blocks, RO membranes, etc. Also need to evaluate product performance as per specifications. He/She will be working under guidance of scientists/chemists. Documentation: Maintain comprehensive and accurate records of all experiments, results, and observations in lab computer. Reporting: Summarize experimental findings and project progress to seniors regularly. Safety and Compliance: Strictly adhere to all laboratory health, safety, and regulatory protocols, including Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GM...

Responsible for QC testing of raw materials, in-process, and finished goods. Maintain documentation, ensure GMP & GLP compliance, handle lab instruments, support production and sales teams, and assist in quality improvement and R&D activities. Required Candidate profile B.Sc. or M.Sc. in Chemistry (Organic/Inorganic/Analytical) with 2–3 years of QC or Production experience. international standards, and lab instruments like pH meter, titration, and moisture meter.

Job Summary Execute downstream process development for biosimilar projects, including chromatography, filtration, tech transfer, scale-up, and data documentation, ensuring compliance with quality and regulatory standards. Key Responsibilities Perform downstream processing using AKTA chromatography (SEC, IEX, HIC, RP), filtration (TFF), virus validation, and cleaning validation. Operate, troubleshoot, and optimize AKTA systems and downstream unit operations. Support tech transfer, process scale-up, and characterization using QbD principles. Prepare and review protocols, reports, and regulatory documents. Collaborate cross-functionally with UPD, ADL, DPD, QA, and manufacturing teams. Ensure ac...

Job Summary: Responsible for executing molecular biology and mammalian cell culture techniques to support cell line development activities including vector construction, transfection, clone selection, and assay development. Ensures compliance with GLP/GDP and timely documentation of all work. Key Responsibilities: Perform molecular biology tasks: gene cloning, cDNA synthesis, plasmid prep, buffer prep, and bacterial culture handling. Execute cell culture work: transfection, minipool generation, cell cloning, media optimization, and early product characterization. Support development and optimization of clone evaluation assays and molecular/protein biology techniques. Maintain lab records (LN...

Follow Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Review scientific literature and patents to identify new product development opportunities. Required Candidate profile Specialty Chemicals / Excipients / Pharmaceutical Field Whatsapp CV on 9724346949

Responsibilities: Analytical Operations: Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG). Operate and maintain analytical instruments :- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus Ensure compliance with GLP, 21 CFR Part 11, and data integrity standards. Review and approve analytical reports and LIMS entries , Quality Systems & Compliance Implement and monitor Quality Management Systems (QMS). Lead investigations for OOS, OOT, Deviations, and Laboratory Incidents. Prepare and review SOPs, STPs, and validation protocols. Ensure audit readiness and support regulatory inspections (USFDA, WHO-GMP, etc.) Documentation & Reporting Maintain ac...

Responsibilities: Lead and oversee the entire Quality Control department operations. Ensure compliance with cGMP, regulatory guidelines, and company quality standards. Review and approve analytical methods, specifications, and validation protocols. Supervise raw material, in-process, and finished product testing. Ensure timely release of batches and materials. Manage laboratory investigations, OOS, OOT, deviations, and CAPA. Coordinate with QA, Production, and Regulatory teams for smooth operations. Handle audits (internal, external, and regulatory) and ensure readiness at all times. Provide training, mentoring, and performance evaluation of QC staff. Drive continuous improvement, cost effic...

Responsibilities: Synthetic Chemistry / Lab Work Perform multi-step organic synthesis of target molecules as per project requirements. Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products. Maintain accurate lab records and notebooks (ELN or manual) as per GLP standards. Process Development Assist in the optimization of reaction conditions to improve yield, purity, and scalability. Conduct literature searches and suggest alternative synthetic routes under supervision. Evaluate critical process parameters through small-scale experiments. Analytical Coordination Coordinate with the analytical team for sample submissions, impurity profiling, and m...

Responsibilities: Project & Team Management Lead and manage multiple API development projects across various stages (Route scouting, lab development, scale-up, validation). Plan and allocate resources effectively among chemists and analysts. Mentor and guide junior scientists on technical and professional development. Process Development & Optimization Design and optimize synthetic routes with focus on yield improvement, impurity profile, and cost reduction. Identify and develop alternate synthetic strategies to mitigate IP challenges or improve process efficiency. Develop robust and scalable processes suitable for commercial production. Technology Transfer Prepare technology transfer docume...

Dear All, We are seeking a highly motivated and talented GLP Specialist to join our innovative team. The ideal candidate will have a strong foundation in formulation development as well in Analytical Development. Location: Hyderabad(Dulapally) Required Experience: 4-7 Years Key Responsibilities: Ensure error-free and real-time documentation as per departmental and regulatory requirements. Prepare and revise departmental SOPs, GTPs, AMCCs, and APMCs for Analytical Development (AD) and Formulation Development (FD) departments. Receive and maintain logbooks, SOPs, and other issued documents from QA in a controlled manner. Ensure laboratory compliance with GLP (Good Laboratory Practices) and GDP...

Managing and leading team and Implement and enhance Quality Management Systems, managing all QA dep activities. Monitor laboratory activities to ensure strict adherence to GLP/cGMP procedures, promoting a culture of quality.

As a Scientist I at the U.S. Pharmacopeial Convention (USP), you will play a crucial role in supporting the development of Reference materials. Your responsibilities will include: - Supporting reaction monitoring, scale up, and final analysis of samples as per monograph/in-house procedures, including method development if required. - Preparing development reports for Synthetic Support projects and being involved in project acceptance. Executing projects per approved test protocols when assigned. - Preparing, executing, and completing IQ/OQ/PQ of new instruments. Indenting the required glassware, chemicals, and columns for the ARD projects. Maintaining GLP and implementing safety procedures w...

As an M.Pharm. in pharmaceutics with relevant experience, you should possess a solid technical understanding of Formulation & Development (F & D), particularly in external liquid preparations like disinfectants and sterilants. Your responsibilities will include conducting preformulation and stability studies, requiring knowledge of cGMP/GLP standards. Additionally, experts can apply for specific assignments to contribute their specialized skills. **Key Responsibilities:** - Conduct preformulation and stability studies - Demonstrate sound technical knowledge in Formulation & Development (F & D) - Specialize in external liquid preparations such as disinfectants and sterilants - Ensure adherenc...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary Under the guidance of Manager-Instrumentation/R&D, responsible for installation...

Opportunity to work with a leading Indian pharmaceutical company Opportunity to drive R&D initiatives About Our Client Our client is a leading Indian multinational pharmaceutical company headquartered in Ahmedabad, Gujarat, with a strong presence in generics, biosimilars, and specialty medicines across more than 85 countries. Job Description The key responsibilities include: Strategic Leadership & Innovation Define and execute R&D strategies for plasma-derived products in alignment with company objectives. Lead the development of new plasma-derived therapeutics: IVIG, Albumin, Factor VIII/IX, Anti-D, etc. Collaborate with executive leadership on pipeline planning and long-term innovation roa...

Job Description Candidate must have a knowledge of analysis of all parameters of effluent as per CCA. Knowledge to carry out Jar test. Knowledge of GLP. Good knowledge of calibration of all equipments using of analysis. ETP Record maintaining