Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
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