40 Job openings found

Responsibilities Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations. Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures. Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms. Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing. Support quality investigations and prepare required ...

min experience 1 -2  yr on HPLC Machine CTC - 2 LAC - 2.8 LAC.   Quality Control Team is responsible for sampling, analysis, Testing, line clearance, release, related documentation and other related Quality Control functions in respect of RM/PM/Finished goods/ in process /Validation and stability samples. Job Responsibilities1. To sample the Incoming RM/Packaging material.2. ...

Job Responsibilities: Online quality checking & FG To give feedback to production & Quality Department regarding online deviations and get the corrective actions To maintain all documentations as per IPQA To help operations maintain GMP Preparation of the In Process analysis reports for QC To lead and monitor IPQA activities in the Pre dispatch samples sending, communication ...

Position:        Officer/Executive - Packing Location:        Daman Experience:    1 - 8 Years Industries:     Pharma  Responsibilities: To finalize Packing plan for weekly and monthly. To allocate work to workforce and perform the critical checks and ensure line clearance at all stages of Packing to implement Current good manufacturing practice. Preparation and ...

JOB DESCRIPTION   07.07.26 139853 HPS/2026/574 Jr. QA Engineer Male 1 1 to 3 DME/B.E Mech 8 Hrs Min. 1-3 years of .experience in any Plastic/Rubber/Petrochemical manufacturing  company Job Responsibilities • Inspect incoming raw materials, in-process production, and finished goods as per specifications.• Identify defects and deviations from approved standards.• Maintain inspection records, reports, and non-conformance logs.• Ensure production processes comply with company ...

Position:      Production Officer Location:      Daman Experience:  1 - 5 Years Industries:    Pharma Responsibilities: Monitor and control daily production activities as per production plan. Ensure manufacturing of tablets, capsules, syrups, or other formulations as per SOPs and GMP guidelines. Supervise machine operation, line clearance, and production manpower. Maintain batch manufacturing records (BMR) and production ...

Position:       QA Officer. Location:       Daman Experience:    1 - 3 Years Industries:     Pharma Responsibilities: Ensure compliance with cGMP, GLP, and regulatory requirements. Review and approve Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and analytical reports. Handle deviations, change controls, CAPA, OOS, OOT, and risk assessments. Conduct line clearance, in-process checks, and shop ...

  Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Perform line clearance and in-process checks. Ensure compliance with cGMP, GDP, and SOP requirements. Handle deviations, change control, CAPA, OOS, and OOT investigations. Prepare, review, and update SOPs and QA documents. Conduct GMP audits and shop floor inspections. Monitor documentation and maintain data integrity. Coordinate with Production, ...

Key Responsibilities Operate tablet coating machines such as Auto Coater / Conventional Coating Machines. Perform machine setup, startup, operation, and shutdown activities. Check coating parameters including: Spray rate Inlet / outlet temperature Pan speed Atomization pressure Prepare coating solution as per BMR (Batch Manufacturing Record). Monitor coating process and ensure uniform coating quality. Handle loading and unloading of tablets safely. Maintain ...

Position:      Asst. Manager/Manager - QA Location:      Kadi - Ahmedabad  Experience:   5 - 7 Years Industries:    Pharma Responsibilities: Quality Assurance & Compliance Ensure compliance with cGMP, GLP, and regulatory requirements (WHO, USFDA, MHRA, etc.) Handle audits (internal, external, regulatory) and ensure audit readiness at all times Review and approve SOPs, BMRs, BPRs, protocols, and reports Documentation Management Oversee ...