Instagram
youtube
Facebook

Analytical R&D Analyst I - Tapi

4-8 years
Not Disclosed
10 June 4, 2025
Job Description
Job Type: Full Time Education: M.Sc., M. Pharm., or Ph.D. 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

 

Analytical R&D Analyst I – TAPI

Date Posted: June 2, 2025
Location: Greater Noida, India, 201306
Company: Teva Pharmaceuticals
Job ID: 62022


Who We Are

TAPI (Teva Active Pharmaceutical Ingredients) is the world’s leading supplier of active pharmaceutical ingredients, with over 350 API products in its portfolio and a history spanning over 80 years. Serving 80% of the top 50 global pharmaceutical companies, TAPI is renowned for its reliability, expertise, advanced technologies, and customer service. With 14 global sites and 4,000+ professionals, we focus on consistent innovation and top-tier R&D.


How You’ll Spend Your Day

  • Conduct analysis of in-process, raw materials, intermediates, and APIs using HPLC and wet chemistry techniques.

  • Perform analytical method development, validation, and method transfer to QC teams.

  • Troubleshoot analytical instruments and manage daily lab challenges.

  • Oversee calibration, qualification, and maintenance of instruments such as HPLC, UV spectrophotometers, Auto-titrators, etc.

  • Conduct literature reviews to support method development and regulatory compliance.

  • Maintain strict GLP, GMP, documentation standards, and EHS compliance during all activities.

  • Understand and apply ICH guidelines, impurity profiling, and forced degradation studies.

  • Support regulatory needs across markets including US, EU, Canada, and others.


Your Experience and Qualifications

Education:

  • M.Sc., M. Pharm., or Ph.D. in a relevant field

Experience:

  • 4–8 years of hands-on experience in Analytical R&D

  • In-depth knowledge of:

    • Analytical method development and validation

    • Regulatory standards for generic APIs

    • HPLC, UV, Auto-titrator operation

    • ICH guidelines and impurity profiling


Reports To

R&D Leadership at Greater Noida Site