Officer Quality Assurance

NuSil Technology, LLC; Dehradun; On-site; INR 600,000 - 1,000,000; Full time

Job summary

Avantor in India is seeking a QA/IPQA professional to drive QMS and in-process QA activities across manufacturing operations in a highly regulated IVD/Medical Devices environment. The role focuses on GMP, ISO 9001 and ISO 13485 compliance, with emphasis on continuous improvement and robust documentation.

You will review SOPs, batch records, calibration schedules and logbooks; manage deviations, CAPA, changes, and audits; collaborate with cross-functional teams to strengthen quality culture and

Qualifications

• Graduate or postgraduate in life sciences or related discipline.
• 2–5 years QA experience, with at least 1 year in the IVD/Medical Devices industry.
• Knowledge of GMP, GDP, Change Controls, CAPA, Deviations, Non-Conformance Management, and Validation practices.
• Familiarity with 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 to ensure 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 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 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.

Skills

Quality Assurance

CAPA

Deviations

Documentation Control

ISO 9001

ISO 13485

GMP

ELISA

MS Office

Communication skills

Education

Life Sciences degree

Tools

MS Office

Job description

Job Description:

The Opportunity:

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.

What We Are Looking For:

• 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.

How You Will Thrive & Create an Impact:

• 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: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.

The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.

We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world.

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at [e-mail] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

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3rd party non-solicitation policy:

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation