The Role
Conducts quality-control analysis of raw materials, in-process and finished products, and stability samples for an OSD formulation plant. Operates and maintains analytical instruments, prepares and reviews COAs, STPs, and SOPs, and ensures cGMP, GLP, regulatory, and data-integrity compliance. Investigates OOS/OOT results and deviations, supports method validation and calibration, and maintains laboratory records and samples.
Summary Generated by Built In
Executive – Quality Control (QC) – OSD Formulation
Key Responsibilities:
Perform analysis of raw materials, in-process, finished products, and stability samples.
Operate and maintain analytical instruments (HPLC, GC, Dissolution, UV, IR).
Prepare and review analytical documents, COAs, STPs, and SOPs.
Ensure compliance with cGMP, GLP, and regulatory requirements.
Handle OOS/OOT, deviations, and investigation reports.
Participate in method validation, calibration, and documentation activities.
Maintain lab records, samples, and ensure data integrity.
Qualification & Experience:
B. Pharm / M. Sc
6–8 years of QC experience in OSD formulation plant.
Skills Required
- B. Pharm or M. Sc degree
- 6-8 years of quality control experience in an OSD formulation plant
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The Company
What We Do
CORONA Remedies Limited is an Ahmedabad-based pharmaceutical company founded in 2004. It develops, manufactures, and commercialises innovative, value-added, evidence-based medicines addressing unmet health needs. Its portfolio focuses on chronic-care and specialty therapeutic areas, including women’s healthcare and pain management. The company operates manufacturing facilities in Gujarat and Himachal Pradesh and aims to improve health outcomes through quality products and research.
