14 Job openings found

Key Responsibilities: Preventive, predictive & breakdown maintenance of plant & utility equipment (Water, Steam, HVAC, Pneumatic, Hydraulic). Ensure compliance with cGMP, cGLP, GDP, GEP & safety policies. Manage validation, qualification, calibration & engineering documentation. Plan and execute preventive maintenance programs to minimize downtime. Coordinate with production & external agencies for timely maintenance. Oversee pest control, site ...

Key Responsibilities: Handle QMS activities including CAPA, Change Control, Deviation, and OOS/OOT. Prepare, review, and maintain QMS documentation as per cGMP and regulatory guidelines. Support internal audits, external audits, and regulatory inspections. Ensure timely closure of quality incidents and continuous improvement initiatives. Coordinate with cross-functional teams for compliance and quality culture. Requirements: B.Pharm / M.Sc (Chemistry) with ...

Job Title: Warehouse Operator – Dispensing (Formulation Plant) Department: Warehouse / Stores – Dispensing Section (Formulations) 📍 Location: [Insert Location] 🕒 Experience: 2 to 5 Years 🎓 Qualification: B.Pharm / M.Pharm / Diploma in Pharmacy (Mandatory) Job Summary: We are hiring a dedicated Warehouse Operator – Dispensing for our Formulation manufacturing facility, responsible for precise ...

  Industry: Pharma Formulation Openings: 10Experience: 3–7 YearsPreference: Male Candidates only / Gujarati-speaking Key Responsibilities: Perform testing of Raw Materials (RM) & Packaging Materials (PM) as per pharmacopoeial standards. Ensure timely release of materials with accurate documentation. Follow cGMP, GLP, and regulatory compliance in QC lab. Maintain records, calibration logs, and SOP adherence. Coordinate with QA, Production, and Warehouse for smooth operations. Requirements: B.Sc./M.Sc. ...

Responsibilities: Operate and monitor capsule filling machines as per SOPs. Perform line clearance, changeover, and basic machine maintenance. Ensure accurate capsule weight, sealing, and batch output. Maintain GMP compliance, documentation, and safety standards. Coordinate with QA/QC for in-process checks. Requirements: ITI/Diploma/Graduate with 2–5 years’ experience in pharma capsule filling. Knowledge of cGMP, SOPs, and machine troubleshooting. Attention to detail ...

Key Responsibilities:  • Ensure effective implementation of QMS elements such as deviation, CAPA, change    control, and risk assessment in production. • Support production teams in initiating and closing QMS records in a timely manner. • Coordinate with QA and cross-functional teams to ensure proper documentation and    follow-up of QMS activities. • ...

Key Responsibilities: Develop and implement production and planning schedules aligned with organizational goals. Manage and monitor inventory levels of raw materials, packaging materials, and finished goods. Coordinate with the formulation development team to ensure product consistency and quality. Maintain accurate BMRs/BPRs and other production documentation as per GMP. Collaborate with maintenance teams to plan and ...

Troubleshoot and repair equipment  Install and maintain heavy machinery, plant equipment, and tools  Use industrial technology to diagnose equipment failures Create maintenance procedures  Optimize equipment, procedures, and budgets  Make production department smooth Handle manpower Provide training to new employees Work under the guidance of departmental manager  Following GMP Following cGMP. 

  Job Title - QC Officer/Executive   Job Responsibilities and required key skills : Titration method (Peroxide value, Free fatty Acid, chemicals Standardization) Equipment Exposure ( HPLC, GC, pH meter) Safety Compliance GLP compliance Good Communication Skills Major Responsibilities:  •On time analysis & release of raw material, in process samples & finished product samples • Ontime Training completion within predefined ...

  Job Overview - Routine Microbial Analysis of Raw Material & Finish Good Samples Routine Calibration Environment Monitoring Media preparation Product Stability Documentation Report Preparation   Responsibilities and Duties- - Prepare monthly, quarterly and annual sampling plan, Validation plan and/or qualification plan - Prepare and implement stability plan for all products. - Daily Reporting and release of Raw materials and finished goods - Co-ordination ...