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    Job · 21683036

    DEHRADUN · FULLTIME

    Officer Quality Assurance

    Avantor

    Avantor

    Dehradun · onsite · Posted 1d ago

    Sourced fromNaukri
    Undisclosed2–5 yrsfulltimeDehradun

    About a minute. You'll make an account on the way through.

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    Section · 01

    About this role

    Job Summary

    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 operations. This 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.

    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.
    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.

    Sourced from naukri

    Section · 02

    Skills

    ISO 13485DiagnosticsISO 9001classificationauditsChemistryHematologyiso standardsCAPACancerIPQAClinical ChemistryDispensingBiotechnologycontractorFabricationManufacturingcomplianceLife Sciencesdispatch

    Section · Company

    About Avantor

    Avantor

    Avantor

    Pharma

    2.0k+

    employees

    1904

    122 years old

    Radnor Township, Pennsylvania

    United States

    About

    Avantor is a leading global provider of mission-critical products and services to customers in biopharma, healthcare, education & government, and advanced technologies & applied materials.

    Industries

    PharmaChemicals / Agri InputsHealthcare

    Employee ratings

    342 reviews

    3.7/ 5

    Culture

    3.5

    Career growth

    2.9

    Work-life

    3.8

    Employees rate it well for

    Work Culture38Salary33Work Life Balance30Senior Management29Job Security22

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