MSc Chemistry Jobs in QC at Avantor | Apply Now For The Quality Control Officer Role
Avantor is hiring a Quality Control Officer in Thane, India (Job ID: R-167313). This role presents an exciting opportunity to contribute to quality assurance in the fine chemicals and pharmaceutical industries. If you have expertise in HPLC, GC, wet analysis, ISO implementation, and cGMP practices, this position could be the next big step in your career.
- Job Position: Quality Control Officer
- Location: Thane, India
- Job ID: R-167313
About the Company
Avantor is a global leader with over 14,000 associates dedicated to advancing life-changing science. The company offers essential products and services that support the pharmaceutical, biotechnology, industrial, educational, government, and healthcare sectors worldwide. Avantor fosters a culture of innovation, inclusivity, and professional growth, offering employees the chance to make a real impact while building a fulfilling career.
Job Description
The Quality Control Officer will be responsible for performing QC activities at AQAL, ensuring compliance with cGMP, ISO, and regulatory requirements. The role involves analysis, documentation, and supporting audits, as well as maintaining high standards of quality in all laboratory operations.
Key Responsibilities
- Conduct timely analysis of samples (RM/Intermediate/Finished Goods).
- Coordinate with tollers to address quality-related issues and seek clarifications.
- Ensure compliance with ATR and assist in ISO implementation.
- Perform sampling, calibration, standard preparation, and documentation.
- Operate and handle HPLC, GC, and wet analysis techniques.
- Record results in SAP and maintain analytical records/log sheets as per GMP & ISO.
- Train and supervise operators while monitoring waste generated during operations.
- Act as a member of the Emergency Response Team.
- Maintain compliance with ISO 9001:2015, SAP, and Quality Systems.
- Strive for zero accidents in quality operations.
Qualifications
- B.Sc. / M.Sc. in Chemistry.
- 2–5 years of experience in Quality Control, including cGMP, ISO, and regulatory audits.
- Knowledge of QC in fine chemicals and pharmaceutical industries.
- Strong documentation and analytical skills.
- Competencies: willingness to learn, team player, good communication skills.
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