QC Jobs in Sikkim: Zuventus Healthcare Ltd. is hiring an Officer – Quality Control
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If you want to establish a career in the pharmaceutical industry and are looking for QC Jobs in Sikkim, here’s an opportunity.
Zuventus Healthcare Ltd. is hiring a dedicated Officer – Quality Control at its Sikkim factory. This role is ideal for B.Pharm graduates with 2–4 years of experience in HPLC and QC operations. The officer will ensure cGMP and GLP compliance, handle investigations of deviations, and review analytical data for finished, in-process, and validation samples, contributing to high-quality pharmaceutical manufacturing..
About the Company:
Zuventus Healthcare Ltd. is a dynamic and forward-thinking pharmaceutical company committed to delivering high-quality healthcare products. Established in 2002 and headquartered in Pune, Maharashtra, Zuventus has rapidly ascended to become one of India’s leading pharmaceutical companies. As of September 2024, it is ranked 9th in its directly covered market and 25th among the leading healthcare companies in India Zuventus. The company operates three state-of-the-art manufacturing facilities in Jammu, Sikkim, and Bengaluru, and a DSIR-approved advanced formulation center in Pune. These facilities enable Zuventus to produce a diverse range of over 170 healthcare products across 16 therapy areas, including anti-infectives, nutritional supplements, cardiovasculars, pain management, respiratory, hepatology, and gastroenterology segments. Zuventus is a wholly owned subsidiary of Emcure Pharmaceuticals, which acquired the remaining 20.42% stake in Zuventus for ₹724.9 crore in June 2025, consolidating its operations and streamlining its business structure The Times of India. The company’s commitment to excellence is reflected in its adherence to stringent quality control standards and its dedication to bringing joy and jubilation into people’s lives through innovative and superior products.
Job Details:
- Job Title: Officer – Quality Control
- Location: Sikkim, India
- Department: Quality Control
Job Responsibilities:
- Monitor cGMP and GLP compliance and ensure adherence to regulatory requirements and filing commitments.
- Investigate deviations such as LIR (Incident / OOS / OOE).
- Review and analyze data reports accurately.
- Conduct analysis of Finished, In-process, Process Validation, and Cleaning Validation samples.
Education: Bachelor of Pharmacy (B.Pharm)
Experience: 2–4 years in HPLC and Quality Control
Skills:
Strong understanding of pharmaceutical QC processes, analytical methods, and regulatory compliance.
