98 Job openings found

Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable). Review and approve analytical results, COAs, test reports, and raw data. Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.). Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.). Review and update SOPs, STPs, GTPs, ...

Job Title: QC ChemistCompany: Concept PharmaLocation: AurangabadCTC: ₹NegotiableExperience: 3 Position: 2–3 years Job Summary Concept Pharma is looking for Quality Control (QC) Chemists to support routine quality testing and compliance activities in a pharmaceutical manufacturing environment. The role involves analytical testing of raw materials, in-process samples, and finished products in compliance with GMP and regulatory standards. Key Responsibilities Perform routine analysis ...

Position:         QA Officer Location:         Vapi Experience:     0 - 1 Years Industries:       Pharma   Responsibilities Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies. LNB's and Logbooks Issuance and Checking for daily entries in Logbooks. To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and Internal Audit Reports. Prepare, ...

Key Responsibilities: Perform in-process checks during manufacturing and packaging (weight variation, hardness, friability, disintegration, pH, viscosity, leak test, etc.). Ensure batch manufacturing records (BMR/BPR) are correctly filled and compliant. Monitor line clearance, environmental conditions, and GMP practices on shop floor. Review and verify critical process parameters (CPP) and ensure adherence to SOPs. Check and approve ...

Position:          QA Officer Location:         Panoli - Ankleshwar Experience:     3 - 5 Years Industries:       Pharma   Responsibilities: Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies. LNB's and Logbooks Issuance and Checking for daily entries in Logbooks. To Review various Documents like Change controls, Incident Reports, CAPA, OOS ...

🔑 Key Responsibilities GMP Compliance Ensure effective implementation of GMP guidelines across production, QA, QC, warehouse, and utilities. Monitor day-to-day GMP activities and identify non-conformances. Support GMP audits (internal, customer, and regulatory). Documentation & Records Prepare, review, and control GMP documents such as SOPs, formats, logs, and registers. Ensure proper documentation practices (GDP) are followed. Maintain training, deviation, ...

Key Responsibilities Conduct routine chemical and physical tests on incoming raw materials, in-process samples, and finished products in accordance with SOPs and quality standards. Perform analytical techniques including titration, pH measurement, and instrument-based analysis (e.g., UV-Vis, chromatography as required). Accurately record, analyze, and interpret data; prepare test reports and maintain detailed laboratory documentation. Ensure ...

Position:          Production Manager Location:         Vapi Experience:      12 - 15 Years Industries:       Pharma - API Responsibilities. Overall responsible for planning and maintenance of optimum inventory of raw materials, in –process and finished goods. To ensure the products are manufactured and stored according to pre-approved instructions to ...

Position:          QC Executive Location:          Daman Experience:      5 - 7  Years Industries:       Pharma   Responsibilities: Incoming Material Inspection Inspect and test incoming raw materials, packaging materials, and components as per approved specifications and sampling plans. Communicate non-conformances to the supplier and QA & Purchase department. In-Process Quality Control Perform in-process checks during production (e.g., dimensional ...

Position:        Production Chemist Location:        Mehsana Experience:     2 - 3 Years Industries:      Pharma - API   Responsibilities: Report to the Production Manager on daily production activities and progress. Ensure adherence to Standard Operating Procedures (SOPs) for cleaning and equipment operations. Comply with Batch Manufacturing Record (BMR) specifications and promptly report ...