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Formulation Researcher I

2-6 years
Not Disclosed
10 July 26, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, 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

Who We Are

At Teva Pharmaceuticals, we are committed to making healthcare more affordable and accessible, improving the lives of millions globally. Our mission unites our diverse team across nearly 60 countries, comprising a rich variety of nationalities and backgrounds. We are the world's leading manufacturer of generic medicines and proudly produce many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people worldwide take one of our medicines daily—a number we aim to grow as we continue to innovate and expand our impact.

The Opportunity

We are seeking a Bench Scientist with a strong analytical acumen in formulation research and development, process development, regulatory affairs, and intellectual property for global markets. The role involves planning and conducting experiments aligned with project milestones, working on products at various stages from selection to launch, and applying scientific principles such as QbD (Quality by Design), DoE (Design of Experiments), and statistical analysis. The ideal candidate will also understand intellectual property scenarios, work on design-around strategies, and coordinate with cross-functional teams to overcome development challenges.

How You’ll Spend Your Day

  • Collaborate with formulation development teams to achieve key project milestones.
  • Plan and conduct experiments using QbD principles, including OFATs and DoE.
  • Prepare presentations and interpret data throughout the product development stages.
  • Conduct literature reviews, prior art searches, and design experiments for new products.
  • Evaluate APIs, excipients, and innovator products; conduct preformulation studies.
  • Manage the execution of development trials, scale-up, and submission batches, addressing any issues.
  • Establish stability data for development batches and prepare master documents.
  • Coordinate with cross-functional teams for smooth product development.
  • Compile pharmaceutical development reports and handle deviations, change controls, and OOS for exhibit batches.
  • Maintain necessary records and SOPs, ensuring compliance with regulatory standards.

Your Experience and Qualifications

  • Education: Ph.D. in Pharmaceutical Sciences with 1+ years of experience, or M. Pharm in Pharmaceutical Sciences with 3+ years of experience from reputed universities.
  • Experience: Proven experience in formulation development of solid oral dosage forms, from development to regulatory submission, in regulated markets (US/EU/Canada).
  • Technical Skills: Knowledge of recent ICH guidelines, bioequivalence, GMP, GLP, and SOP compliance.
  • People Skills: Confident team player with strong interpersonal skills, able to collaborate across teams and work independently.
  • Interpersonal Skills: Strong technical communication skills, capable of delivering presentations and contributing to global project teams.

Reports To

This position reports to the Manager/Sr. Manager/Associate Director, Generic R&D.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. Our global policy ensures that equal employment opportunities are provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally recognized status entitled to protection under applicable laws. We are dedicated to fostering a diverse and inclusive workplace. If contacted for a job opportunity, please inform us of any accommodations needed during the recruitment and selection process. All accommodation information will be treated confidentially and used solely for providing an accessible candidate experience.