Pharma QA Jobs at Innova Captab Ltd

Pharma QA Jobs at Innova Captab Ltd, Apply on Rasayanika

Quality Assurance at Innova Captab Ltd

Role: Quality Assurance

Company: Innova Captab Ltd

Qualification: BSc/MSc/BPharm/MPharm in any specialization

Budget: Based on current CTC, 10-12% hike

Interview Mode: F2F/Virtual

Location: Jammu & Kashmir

Experience: 1-4 years

Key Responsibilities

  • Review & approval of batch manufacturing records (BMR), batch packing records (BPR) and other production documentation to ensure accuracy, completeness, compliance with SOPs and regulatory requirements.
  • Line clearance/production release: Ensure that production/packaging area is ready for manufacturing, all preceding steps are completed properly.
  • In-process checks and sampling: Ensure that in-process control points are monitored as per defined specifications.
  • Monitoring use of raw materials, packaging materials, ensuring correct identification, storage, labeling, etc.
  • Assist in managing deviations, investigations of non-conformances / Out of Specification (OOS) results, and follow up with appropriate corrective and preventive actions (CAPA).
  • Change control: Review and ensure proper documentation and approvals for changes in process, materials, equipment, etc.
  • SOPs / Work Instructions: Assist in drafting, reviewing, updating, and ensuring adherence to SOPs and other regulatory documents.
  • Quality audits & inspections: Support internal audits and ensure audit findings are addressed; assist during external regulatory audits or customer audits.
  • Product Quality Review (PQR):
    Assist in gathering data and documentation for periodic reviews.
  • Ensure compliance with good manufacturing practices (GMP), Good Documentation Practice (GDP), applicable guidelines and regulations.
  • Support cross-functional coordination with Production, QC, Regulatory Affairs, Engineering, etc., to ensure quality compliance.
  • Maintain records, archives, documentation in an organized manner.
  • Participate in training sessions for quality systems, regulatory requirements, SOPs, etc.

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