Officer Quality Assurance
VWR International · Dehradun · onsite · Posted 42d ago
Undisclosed2–5 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Job Summary
Requirements
Responsibilities
Disclaimer This job posting has been aggregated from external sourceRole details, content, and availability are subject to changeApplicants are advised to confirm the latest information directly on the company website before applying.
The incumbent will play a key role in ensuring product quality, regulatory compliance, and operational excellence by driving Quality Management System (QMS) and In-Process Quality Assurance (IPQA) activities across manufacturing operationsThis role offers an opportunity to contribute to a highly regulated IVD/Medical Devices environment, supporting continuous improvement initiatives while ensuring adherence to GMP, ISO 9001, ISO 13485, and quality standards.
Requirements
- Graduate/Post-Graduate in Life Sciences, Biotechnology, Microbiology, Chemistry, Pharmacy, or a related discipline.
- 2 to 5 years of Quality Assurance experience, including at least 1 year in the IVD or Medical Devices industry.
- Sound knowledge of GMP, Good Documentation Practices (GDP), Change Controls, CAPA, Deviations, Non-Conformance Management, and Validation practices.
- Knowledge of ISO 9001, ISO 13485, regulatory requirements, and audit processes.
- Understanding of ELISA, Clinical Chemistry, Rapid Diagnostics, Hematology, and related manufacturing processes.
- Proficiency in MS Office and quality documentation management.
- Strong communication, problem-solving, time management, and stakeholder management skills.
Responsibilities
- Execute IPQA activities across fabrication, dispensing, manufacturing, packaging, and dispatch operations to ensure consistent product quality and compliance.
- Review and maintain SOPs, batch records, calibration schedules, logbooks, and technical documentation.
- Drive quality improvements by identifying deviations, non-conformances, and process risks, while ensuring timely investigations and CAPA implementation.
- Support QMS activities including handling of market complaints, Change Controls, audits (internal external), training initiatives, and compliance programs.
- Ensure adherence to GMP, GDP, ISO standards, safety requirements, and records management practices.
- Collaborate effectively with cross-functional teams to strengthen quality culture and operational excellence.
- Contribute to the delivery of safe, compliant, and high-quality products through a proactive, detail-oriented, and continuous improvement mindset.
Disclaimer This job posting has been aggregated from external sourceRole details, content, and availability are subject to changeApplicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
ISO 13485DiagnosticsISO 9001classificationauditsChemistryHematologyiso standardsCAPACancerIPQAClinical ChemistryDispensingBiotechnologycontractorFabricationManufacturingcomplianceLife Sciencesdispatch
About VWR International
VWR International
Pharma
92
employees
1852
174 years old
Radnor, Pennsylvania
United States (USA)
₹5.4L PA avg
Avg at VWR International
About
VWR International is a global provider in life sciences and advanced technologies, facilitating procurement and distribution of essential lab and production materials.
Industries
PharmaBiotech & Life sciencesRetail
Employee ratings
10 reviews
3.6/ 5
Culture
4.1
Career growth
3.4
Work-life
3.9
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