Officer

Glenmark Pharmaceuticals; Solan; On-site; INR 300,000 - 540,000; Full time

Job summary

Glenmark Pharmaceuticals in Himachal Pradesh seeks IPQA professional to perform on-floor QA activities at all manufacturing and packing stages. You will review batch records, documents related to manufacturing, packaging and analysis prior to batch release, and ensure compliance with SOPs, BPR and master records.

Knowledge of APQR/CPV processes and clean-room hygiene is preferred. The role involves cross-functional QA oversight from receipt of material to dispatch, with emphasis on documentation

Qualifications

• Experience in IPQA activities on the shop floor across manufacturing and packing.
• Knowledge of batch processing records and related documentation.
• Familiarity with APQR and CPV processes.
• Ability to review SOPs, specifications, BPR issuance, and master records.
• Understanding of clean room behavior and personnel hygiene.

Responsibilities

• Conduct IPQA activities for dispensing, manufacturing, packaging and dispatch.
• Review and control of SOPs, specifications, BPR issuance, Master Formulae and Records.
• Oversee QA overview for receipt of material from warehouse to production.
• Review of documents of respective areas and logbooks for adequacy and completeness.
• Ensure batch records are complete and ready for batch release.

Skills

IPQA processes

Quality Assurance

Documentation review

GMP understanding

Job description

Job Description
To perform IPQA activities at shop floor in each and every stage of manufacturing and packing.

• QA overview for clean room behaviour and personnel hygiene .
• Review of batch processing records.
• Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.
• Knowledge of APQR and CPV process
• Review of documents of respective areas and logbooks for adequacy and completeness.
• QA overview for receipt of material from warehouse to production.
• IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities.
• Review and Control of SOP's, Specification, BPR issuance, Master Formulae and Records.