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Pharm Products Pvt Ltd, a leading pharmaceutical manufacturer in Thanjavur, Tamil Nadu, is hiring a Quality Control / Regulatory Affairs Executive to strengthen its Quality Assurance team.
If you are a B.Pharm or M.Pharm graduate with 1–5 years of experience in pharmaceutical quality control and a strong grasp of GMP, GDP, and regulatory compliance, this is your opportunity to make a significant impact in the healthcare manufacturing sector.
Key Responsibilities
- Perform analytical testing of raw materials, in-process samples, and finished formulations using HPLC, GC, UV-VIS, and FTIR techniques.
- Conduct microbiological and stability testing, including environmental monitoring.
- Maintain accurate, GMP- and GDP-compliant documentation for all quality operations.
- Prepare and review Certificates of Analysis (COA) and quality-related records.
- Identify deviations, conduct root cause investigations, and support CAPA implementation.
- Collaborate with Production, QA, and R&D teams to ensure regulatory adherence.
- Assist in method validation and participate in internal quality audits.
- Train and mentor junior staff on testing procedures and quality systems.
- Stay updated on FDA, EMA, and other global regulatory standards.
Qualifications & Skills
- Education: B.Pharm or M.Pharm (preferred).
- Experience: 1–5 years in pharmaceutical Quality Control.
- Technical Expertise: HPLC, GC, FTIR, UV/Vis spectroscopy, analytical method validation.
- Knowledge: GMP, GDP, FDA/EMA compliance.
- Soft Skills: Attention to detail, analytical thinking, teamwork, and communication.
- Certifications: Quality Auditor or Six Sigma (added advantage).
Benefits
- Competitive salary based on experience (₹3.5–6.5 LPA).
- Exposure to advanced analytical and regulatory systems.
- Training and development opportunities.
- Stable career in a reputed pharmaceutical manufacturing organization.
Location
📍 Thanjavur, Tamil Nadu, India
This is a full-time, on-site position.
How to Apply
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