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.
🔹 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
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
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
🧠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
💰 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
📩 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.