The Quality Assurance (QA) department is expanding, opening exciting career opportunities for professionals in the pharmaceutical sector. If you have experience in FDA-regulated environments and a strong understanding of cGMP practices, this is a great opportunity to advance your career.

Multiple roles are available across QA functions including Documentation & Review, Stability, and Vendor Qualification. Candidates with relevant experience and a passion for quality systems are encouraged to apply.

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🔹 Open Positions

Officer – QA (Documentation & Review)

Key Responsibilities

• Review manufacturing and packaging documentation
• Retrieve and review batch records as per cGDP, cGMP, CPC SOPs, and FDA guidelines
• Perform batch data entry for Annual Product Review (APR) and process validation
• Prepare APR / Product Quality Review (PQR) reports
• Review process validation reports

Qualification

• B. Pharm / M.Sc
• 2–4 years of experience in FDA-regulated QA environments

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Officer – QA (Stability)

Key Responsibilities

• Prepare, review, and approve stability protocols, reports, and SOPs
• Analyze stability data for expiry and regulatory compliance
• Evaluate stability impact under change control
• Investigate deviations, OOS, and atypical results
• Maintain stability data in ERP/QMS/LIMS systems

Qualification

• B. Pharm / M.Pharm / M.Sc
• 2–4 years of relevant experience

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Officer/Executive – Vendor Qualification

Key Responsibilities

• Review and approve vendor audit documentation
• Coordinate with suppliers for quality agreements
• Maintain audit certifications and compliance records
• Review batch manufacturing and packaging records

Qualification

• M.Pharm / M.Sc
• 1–2 years of experience

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🧠 Required Skills

• Strong understanding of cGMP, US FDA, and EU regulatory requirements
• Knowledge of pharmaceutical manufacturing and packaging processes
• Proficiency in MS Office (Word, Excel, data analysis)
• Excellent documentation and communication skills
• Strong attention to detail and ability to work in fast-paced environments

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💰 Salary & Benefits

• Estimated Salary Range: ₹3.0 LPA – ₹8.0 LPA (based on role and experience)
• Opportunity to work in FDA-regulated environments
• Career growth in Quality Assurance domain
• Exposure to global regulatory standards
• Professional development and learning opportunities

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📩 How to Apply

Interested candidates can share their updated resumes via email:

Email: ketan.dalki@cpc.com

Make sure your resume highlights your QA experience, regulatory exposure, and relevant skills for better shortlisting chances.