Analytical R&D Analyst I - Tapi

Teva Pharmaceuticals

3-5 years

Not Disclosed

Gwalior India

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.

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Analytical R&D Analyst I - Tapi

Job Description

About Teva Pharmaceuticals:

The Opportunity:

Key Responsibilities:

Qualifications:

Skills & Competencies:

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