Senior Executive – Quality Control (Diagnostics / IVD) at Meril | Apply now for Pharma Jobs Opportunity
If you are searching for Executive Jobs in the growing diagnostics sector, this opportunity is one of the most promising Pharma Jobs available in Gujarat. Meril is hiring a Senior Executive / Assistant Manager – Quality Control (Diagnostics / IVD) for its Vapi/Daman location. This role is ideal for professionals with 3–10 years of experience in QC testing of Rapid, ELISA, and PCR products who want to grow their careers in high-quality Pharma Jobs within the medical devices industry.
- Position: Senior Executive / Assistant Manager – Quality Control (Diagnostics / IVD)
- Location: Vapi / Daman, Gujarat, India
About the Company
Meril is a fast-growing global medical device organization committed to quality and innovation in healthcare diagnostics. Operating in the Medical Devices – Diagnostics (IVD) sector, the company focuses on delivering reliable and compliant diagnostic solutions. Professionals seeking long-term growth in Executive Jobs and Pharma Jobs can benefit from Meril’s strong regulatory framework and innovation-driven culture.
Job Description
We are looking for an experienced Quality Control professional to join our growing Diagnostics division. If you have hands-on experience in Rapid, ELISA, and PCR-based products, we would love to connect with you.
This opportunity under Executive Jobs is designed for candidates with expertise in QC testing, documentation, and regulatory compliance within the Diagnostics/IVD manufacturing sector.
Key Responsibilities
- QC testing of Raw Materials (RM), Semi-Finished Goods (SFG), and Finished Goods (FG)
- Testing of Rapid diagnostic kits, ELISA & PCR products
- Method validation & verification
- Specimen panel preparation
- Handling OOS/OOT, deviations & investigations
- Maintaining documentation as per ISO 13485, GLP & GDP
- Supporting audits and regulatory compliance
Qualifications
- M.Pharm / B.Pharm
- M.Sc / B.Sc (Chemistry / Biotechnology or relevant Life Sciences)
Requirements
- 3–10 years of QC experience in IVD / Diagnostic manufacturing
- Strong knowledge of ISO 13485, GLP & GDP
- Experience in QC documentation and regulatory compliance
- Preferred: Experience with Rapid / ELISA / PCR product testing
