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Analytical R&D Analyst I - Tapi

3-5 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Analytical R&D Analyst I - TAPI
Location: Gwalior, India, 244235
Company: Teva Pharmaceuticals
Job ID: 60743
Date: February 10, 2025

About Teva Pharmaceuticals:

Teva Pharmaceuticals is a global leader in the supply of active pharmaceutical ingredients (APIs) through its TAPI division. With an extensive portfolio of over 350 API products, Teva serves 80% of the top 50 global pharmaceutical companies. With more than 80 years of expertise, Teva’s TAPI division is a trusted supplier of APIs, leveraging cutting-edge technologies and outstanding customer service. Teva employs over 4,000 professionals across 14 global sites.

The Opportunity:

Teva is seeking an Analytical R&D Analyst I to join the TAPI team in Gwalior, India. The role involves contributing to method development and providing routine analytical support for raw materials, intermediates, in-process samples, and drug substances. The ideal candidate will have hands-on experience with analytical techniques and instrument calibration, along with an understanding of stability studies and ICH guidelines.

Key Responsibilities:

  • Method Development: Participate in method development and provide routine analytical support to pilot and CRD for raw materials, intermediates, in-process samples, and drug substances.
  • Analytical Techniques: Use various analytical techniques including HPLC, UPLC, GC, GC-MS, FTIR, PSD, TGA, KF, and auto titrator.
  • Stability & Forced Degradation Studies: Conduct stability and forced degradation studies for drug substances in compliance with ICH guidelines.
  • Instrument Calibration & Maintenance: Perform calibration and maintenance of sophisticated instruments such as HPLC, GC, IR, Karl Fischer, and melting point analyzer.
  • Routine Analysis: Conduct routine analysis of CRD and pilot samples according to established procedures.
  • Documentation: Ensure accurate documentation as per GMP requirements.
  • Safety & Compliance: Adhere to lab safety norms, ensure compliance with GLP, and maintain a safe work environment.
  • QC Support: Provide necessary support to the QC team during validation batches and routine tasks when required.
  • Regulatory Support: Assist with regulatory or customer-related tasks for commercial and pipeline products as needed.
  • Training & Development: Participate in departmental training and discussions.

Qualifications:

  • Educational Requirement: MSc. in Organic Chemistry or Analytical Chemistry.
  • Experience: 3 to 5 years of relevant experience in analytical research and development.

Skills & Competencies:

  • Proficiency in wet chemistry and various analytical techniques (e.g., HPLC, UPLC, GC, FTIR).
  • Knowledge of ICH guidelines related to stability and forced degradation studies.
  • Experience in instrument calibration and maintenance.
  • Strong documentation skills in compliance with GMP.
  • Ability to work in a collaborative environment and contribute to team goals.

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For more details, visit Teva Pharmaceuticals Careers.