Officer -QA

Lupin

Mangan

On-site

INR 500,000 - 800,000

Full time

2 days ago
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Job summary

Lupin in India seeks a quality/compliance professional to ensure cGMP adherence on the shop floor. You will perform line-clearance, in-process checks, and sampling at various manufacturing stages, ensuring no cross-contamination and timely release of batches.

You will review master batch records in SAP, support investigations into product or system failures, and train technicians on SOPs and cGMP requirements to sustain manufacturing quality.

Qualifications

  • Graduation in Pharmacy is required.
  • 2–4 years of relevant experience in manufacturing/compliance.
  • Familiarity with cGMP regulations.

Responsibilities

  • Ensure compliance with cGMP and SOPs on the shop floor.
  • Perform line clearance and prevent contamination during manufacturing.
  • Conduct in-process checks at various stages and document results.
  • Sample at different stages per requirements.
  • Review master batch manufacturing and batch packing records in SAP.
  • Investigate product and system failures; participate in CAPA.
  • Train technicians on cGMP and SOPs.

Skills

Line clearance
In-process checks
Sampling

Education

Graduation in Pharmacy

Tools

SAP

Job description

Job Description:

Job Description

Compliance to the instructions given in Batch records of various products.

Ensuring the compliance of the SOPs and cGMP requirements at shop floor.

Ensuring no mix-ups, contamination and cross contamination of the products during all stages of manufacturing means of “Line Clearance” and continuous monitoring the process.

Performing “In-process Checks” at different stages of manufacturing for various products and ensuring the compliance.

“Sampling” at different stage of manufacturing or as per the requirement.

Stage wise review of batch records and compliances if any, to facilitate timely release.

Preparation, execution and compilation of process validation (Process performance qualification) and cleaning validation & cleaning verification.

Review of master batch manufacturing record and batch packing record in SAP.

Active participation in investigation related to product / system failure.

Ensuring the awareness of cGMP and its requirement to the technicians/concerns through continuous interaction/SOP training.

Work Experience

2-4 years

Education

Graduation in Pharmacy

Requirements:

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