1074 Glp Jobs - Page 15

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

As a qualified candidate, you will be leading the Quality Assurance, QC Chemistry, and Microbiology Laboratories for the site. Your role will involve developing Standard Operating Procedures (SOPs), ensuring compliance with current Good Manufacturing Practices (cGMP) and regulatory guidelines, and monitoring day-to-day department activities. Responsibilities include reviewing and approving documents, executing in-process controls, participating in investigations, vendor qualification, stability management, and ensuring safety practices. - You will be responsible for organizing the recruitment and training of QA (Quality Assurance) and laboratory personnel for chemistry and microbiology labor...

Role Overview: You should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of relevant experience. Immediate joiners are preferred for this position. As a member of the team, your responsibilities will include conducting HPLC analysis of Solid Orals and Nasal products, hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products, as well as ensuring compliance with GMP/GLP practices. The preferred candidate will have 2-8 years of experience and prior exposure to working in regulated plants, specifically those approved by USFDA/MHRA. Key Responsibilities: - Conduct HPLC analysis of Solid Orals and Nasal pro...

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, R&D, and Supply Chain for quality-related activities. Support impl...

A Quality Control Manager oversees and manages quality control processes to ensure products and services meet established standards, customer expectations, and regulatory requirements. Responsibilities include developing and implementing QMS policies Required Candidate profile M.Sc - B. Sc - M. Pharma - B. Pharma Must be able handle department independently in Medium Scale Pharma Company Knowledge to get Prepare necessary documents for Pharma Company FDA requirements

As a Junior Research Scientist Quality at Cholayil Private Limited, your role will be crucial in maintaining the highest standards of product quality and safety across the portfolio. Your responsibilities will include: - Independently managing instrumental and chemical analytical laboratories with precision and discipline. - Leading analytical method development and validation for new and existing products. - Conducting stability studies to evaluate product shelf life and performance under various conditions. - Implementing and maintaining Quality Management Systems (QMS) and supporting internal and external audits. - Overseeing document and data control to ensure traceability and regulatory...

Role Overview: You will be working as an Executive - QC in the Small Molecule Bioanalytical Research Laboratory at Syngene International Ltd. in Bangalore, India. Your main responsibility will be to review data for BA/BE studies in the laboratory, including checking method development, validation, and sample analysis data. You will report to the Head / Group Leader of the Small Molecule Bioanalytical Laboratory. Key Responsibilities: - Perform data checks (QC) for method development, validation, and study sample analysis. - Review STPs, Protocols, validation, and bioanalytical reports. - Ensure necessary documents and records are updated and ready for audits (Sponsor / Regulatory). - Handle ...

As a Quality Control professional at PPL Digwal, your role will involve performing chemical and instrumentation analysis for various stages of production to ensure compliance with GMP and safety standards. You will be responsible for allotting work to the chemists, calibrating instruments, maintaining documentation, managing stock levels of standards and chemicals, and ensuring timely analysis and release of products. Key Responsibilities: - Perform chemical and instrumentation analysis for in-process, raw materials, intermediates, and finished products to meet production schedules. - Allocate work to chemists within the QC department. - Conduct instrument calibrations according to the sched...

As a Validation Specialist at our company, your primary responsibility will be to plan, execute, and document analytical method validation activities for raw materials, in-process samples, finished products, and cleaning validation. This will involve assessing various parameters like accuracy, precision, specificity, linearity, robustness, LOD/LOQ, and others. You will also review and approve validation protocols and reports to ensure compliance with ICH Q2(R1), USP, and other regulatory standards, maintaining adherence to GMP, GLP, and cGMP guidelines. Your role will require collaboration with R&D, QA, and Production teams to facilitate seamless tech transfer and validation support. Trouble...

This role will develop experimental approaches and will be responsible for analyzing scientific results from experiments. Generating accurate, reliable data by following established procedures and practices to support product development. Responsible for formula optimization experiments and process optimization trials by employing the concept of Identification of Quality Target Product Profile (QTPP), Critical Material Attributes (CMAs), Critical Process Parameters (CPPs) and its effect on drug product Critical Quality Attributes (CQAs) during the initial drug product development stage. Responsible for assisting in execution of early development, scale-up, stability, submission, placebo batc...

Good knowledge of analysis. well versed with HPLC, IR, KF,UV and other instrument. Preferred candidate profile Minimum 1 year of experience in HPLC

On-site assessment and selection of target trainees and hospitals to ensure the selections result in optimal quantity and quality of trainees and Phaco conversion rates for the Phaco Development Program. Onsite (Operating Room) and wet lab instruction and consultation of trainees in the entire process of converting from ECCE and SICS to Phaco. This includes working with designated outside-Alcon consultants (course instructors and on-site proctors) to ensure effective trainee Phaco conversion rates and high quality surgical results Demonstrate product and procedural excellence to best technical model and coach trainees and affiliated personnel how to achieve optimal surgical and patient resul...

As a Consultant, you will be a key resource on client engagement. Be up to date with key technical and functional skills, and industry trends Skills and attributes for success Experience in Transfer Pricing and/or direct tax domain Skills and attributes To qualify for the role you must have Qualification Chartetred Accountant/ Postgraduate in Economics / MBA Finance Experience Prior experience/insight into Transfer Pricing Regulations (India and OECD) and/or India Income Tax provisions are desirable.

Job Description: We are looking for a motivated and detail-oriented Research Associate to join our Analytical R&D team within the Peptide Synthesis division. The selected candidate will support the development and execution of analytical methods for peptide characterization, working closely with cross-functional teams in R&D and Quality. Key Responsibilities: Assist in developing and performing analytical methods (e.g., HPLC, UPLC, UV, FTIR, KF, LC-MS) for the characterization and quality assessment of peptides Conduct routine testing of raw materials, intermediates, and final peptide products Support method validation, transfer, and troubleshooting under the guidance of senior scientists Do...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a full-service Global Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland) and London (UK), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Department: Bioanalytical Operations Designation: Research Associate Job Location: Ahmedabad (Gujarat) Job Description: To develop and validate Bioanalytical methods. To process / analyze samples of allotted projects. To operate, calibrat...

GxP, GLP, regulatory environments Support Analyst Role: Support Analyst / Application Administrator We are seeking a highly motivated Support Analyst to provide application administration, user support, and issue resolution for computer systems used across Early Development. This role acts as a technical liaison between IT and end users, ensuring optimal system performance and compliance with regulatory standards. Key Responsibilities: Act as SME for assigned applications supporting users, troubleshooting issues, and managing system documentation. Handle user access control, perform audits, and maintain compliance documentation (GLP/SOP). Coordinate application deployments, upgrades, validat...

As an R&D Associate Cosmetics/Skincare at Vilvah, you will play a crucial role in researching, formulating, and developing high-quality skincare and haircare products that align with our clean beauty and sustainability values. Your expertise in cosmetic science, formulation skills, and creative approach to product innovation will be key to your success in this dynamic and rapidly growing Direct-to-Consumer Ecommerce brand. **Key Responsibilities:** - Research emerging consumer trends, active ingredients, product formats, and packaging innovations in the beauty & personal care industry. - Conduct bench-scale experiments for new product development and validate performance through standard tes...

As the Quality Compliance Senior Manager at Amgen, you will play a crucial role in the Clinical & Research Quality (CRQ) team within the R&D Quality Organization. Your responsibilities will include providing leadership to maintain excellence in R&D Quality Processes, mentoring Amgen staff in India, managing day-to-day activities, and ensuring compliance with regulations globally. You will also support the digital quality management system (DQMS) and provide end-to-end quality support for managing Quality Incidents/Quality Events. Your key responsibilities will include: - Overseeing deviations, audits, and inspections across R&D Quality - Managing the Amgen India R&D Quality team - Facilitati...

Designation : Junior Analyst / Analyst / Senior Analyst Department : Residue / N&W Location : Hyderabad Qualification : M.Sc. (Organic Chemistry/Chemistry/Analytical chemistry) Experience : 1 - 5 Years Industry : CRO & Testing Laboratory Roles and Responsibilities: Analysis of Pesticide residues of Food and Agriculture products as per SOPs, IS, AOAC, FSSAI. Method development, validation and report preparation. Operation and Calibration of equipment i.e., LC-MS/MS, GC-MS/MS, Analysis of Pesticide residues in Water samples. Analysis of Antibiotics in Aqua & Marine products, Feed, Milk & Milk products. Analysis of Pesticide Residues in Fruits and vegetables, Milk & Milk products, Feed & Feed P...

Role & responsibilities 1. To daily analytical planning within the team to deliver results to production team within agreed analytical timeline. 2. To monitor & procure the required essential items like, chemicals, reagent, glassware, columns, spares, consumables, gas cylinders etc. 3. To manage all qc equipments periodically servicing and maintenance at the time of break dawn. 4. Supervision of all chemists work which are distributed. 5. To ensure all qc instruments periodically calibrated & preventive maintenance program. 6. To ensure all raw material, in process & Finished products analysis report review and monitoring online analysis & its documentation. 7. To prepare the Standard Operat...

A QC Officer performs visual inspections, tests, and measurements on raw materials, in-process products, and finished goods. This is done to identify any defects or deviations from the quality standards and specifications. Required Candidate profile Previous experience in a quality control, quality assurance, or manufacturing environment is highly valued. A strong understanding of quality control principles, testing methods

Vibonum Technologies Private Limited, a part of the esteemed Althera Group, is conducting a Walk-in Interview to hire Quality Control professionals for its state-of-the-art OSD manufacturing facility in Nanjangud, Mysore . Department: Quality Control Work Location: OSD Plant, Nanjangud, Mysore Interview Date: September 28th 2025 Time: 09.00 am to 05.00 pm Venue: Hotel Kinara Residency # 2-1, S R Chambers, Beside BSNL Building, Chandannagar, Hyderabad - 500050 20 Open Positions: Assistant Manager / Sr. Executive / Executive / Sr. Officer Eligibility: Education: B. Pharm / M. Pharm / M. Sc Exp: 6-8 Years ------------------------------------------------------------------------------------ Job R...

Roles and Responsibilities: - Authorize release of test report based on the Buyers protocol & test methods - On time responds to Buyers & clients queries, emails and calls - Responsible for reviewing revisions, updates on test parameters, protocols and regulations, etc. and circulating these to the concerned lab team - Training lab staff as per updated, revised protocol received from clients and brands - Support team to develop capability on new test parameters as received in buyer protocol - Training & Supervising the handling, operating and maintenance of test equipment. - Supervising preparation and maintenance of document as per requirement of ISO 17025 - Monitor accuracy of ILC/ PT prog...

GC, HPLC, UV, Malvern, LCMS | SOPs, MSDS, COA | 5S, NABL, GLP, IMS | Reports | Impurity Profiling Inventory, AMC, CMC & LIMS management. Monthly/Yearly report preparation. Audit exposure

Req ID: 329333 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now. We are currently seeking a Business Intelligence Specialist to join our team in Bangalore, Karn?taka (IN-KA), India (IN). Trakwise support resource Trackwise L2 Support for onprimse and Digital version of trackwise for a lifesciences client. Strong understanding of drug discovery or related life science industry experience is required. Strong knowledge in GLP/ GMP process / GXP process Need overall 3/ 4 yrs experience in supporting L2 TrackWise . Work independently on the L2 suppor...