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Quality Control Analyst

7+ years
Not Disclosed
10 Dec. 2, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Quality Control Analyst – Chennai, India
Company: Teva Pharmaceuticals
Job ID: 64273
Date Posted: November 27, 2025
Location: Chennai, India – 600113


About the Company

Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to making healthcare accessible and affordable worldwide. Operating across nearly 60 countries, Teva’s products serve over 200 million people every day. The company continues to drive innovation in quality, compliance, and scientific excellence while expanding access to essential therapies listed by the World Health Organization.


Role Overview

The Quality Control Analyst will be responsible for conducting stability analysis, operating laboratory instruments, ensuring regulatory compliance, and maintaining high standards of data integrity. The role requires strong expertise in analytical techniques such as HPLC and UV, aligned with global laboratory and documentation practices.


Key Responsibilities

Analytical Testing & Reporting

  • Perform stability testing (Assay, Related Substances, Dissolution) for various formulations using HPLC and UV techniques.

  • Prepare samples and execute analytical procedures as per approved Method of Analysis.

  • Review and interpret chromatographic data and ensure accurate, compliant documentation.

  • Evaluate results and promptly report abnormalities or deviations.

Instrument Operation & Maintenance

  • Operate, calibrate, and maintain analytical instruments including HPLC, UV spectrophotometers, and associated systems.

  • Ensure optimal functioning of laboratory equipment and software.

Compliance & Documentation

  • Follow Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and relevant regulatory guidelines.

  • Maintain data integrity across all analytical activities.

  • Ensure adherence to internal procedures and safety guidelines, including usage of PPEs.

Laboratory Management

  • Maintain assigned laboratory workspace, instruments, and equipment.

  • Ensure timely completion of mandatory training and continuous skill development.


Required Qualifications & Experience

  • Education: M.Sc. in Chemistry

  • Experience: Minimum 7 years of hands-on industry experience in Quality Control, specifically in analytical method execution, HPLC/UV analysis, and stability studies.


Why Join Teva Pharmaceuticals?

At Teva, employees contribute to a meaningful mission: improving global health through accessible, reliable medicines. The organization fosters inclusive growth, scientific excellence, and professional advancement.


Internal Applicants

Current Teva employees should apply via the Internal Career Site through Employee Central to receive priority consideration and access exclusive internal opportunities.


Equal Employment Opportunity

Teva Pharmaceuticals maintains a strict commitment to equal employment opportunity and a diverse, inclusive workplace. All qualified applicants will be considered without discrimination on any legally protected basis. Accommodations are available upon request for all stages of the recruitment process.