"Get Paid to Develop Life-Saving Medicines - Teva Pharmaceuticals Formulation Researcher Job!"

Teva Pharmaceuticals Formulation Researcher Job! Apply Online Now

Formulation Researcher I

Date: Apr 24, 2024

Location: Ambernath, India, 421506

Company: Teva Pharmaceuticals

Job Id: 55553

Who we are

Together, we’re on a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. It’s a mission that unites our people across nearly 60 countries, fostering diversity and a variety of nationalities and backgrounds. Working here means being part of the world’s leading manufacturer of generic medicines and a proud producer of many products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people worldwide take one of our medicines daily. It’s an impressive number, and we continually seek new ways to make a difference and welcome new people to join us in making that difference.

The opportunity

Bench scientist with strong analytical acumen in formulation research and development, process development, regulatory, and intellectual property for global markets. Responsibilities include planning and conducting experimentation in line with project milestones. Candidates should have worked on products at different stages from selection to launch, applying scientific principles of QbD, DoE, statistics, and scale-up principles.

Applicants should have the ability to comprehend facts and

data from literature reviews and present the information effectively for decision-making. Understanding the IP scenario and working on various design-around strategies, searching prior art, and experimentally establishing proof of concept are key aspects of the role. Identifying challenges and bottlenecks during development and suggesting mitigation strategies at various stages is also important.

Coordination with CFTs, including MS&T, QA, QC, and production across different geographies for technology transfer and timely execution of submission batches, is essential. Problem-solving skills are needed to identify problems, gather facts, and facilitate analysis for formulation development and process issues.

Prioritizing activities with leads for experimentation in the lab, participating in the execution of development trials and submission batches, and further during commercialization is required. Day-to-day activities must align with established milestones, including the execution of batches at the global TGO operation site. Clear communication with internal stakeholders to identify challenges and risk areas that may hinder timely product delivery is necessary.

Your experience and qualifications

  • Ph.D. in Pharmaceutical Sciences with 1 year of experience or M.Pharm in Pharmaceutical Sciences with 3-7 years of experience from reputed universities.
  • Experience working in a high-performance team in known generic spaces/organizations with a known generic footprint in regulated markets (e.g., US, EU, Canada).
  • Technical skills in formulation development of solid oral dosage forms, exposure from development and submission to regulatory agencies.
  • Uses established processes, scientific theories, and principles to solve problems.
  • Strong learning acumen.
  • Basic understanding of recent ICH and regulatory guidelines, IP requirements, bioequivalence, GMP, quality and SOP compliance, GLP, and other relevant concepts.

Skills and Specific Knowledge Required

  • People Skills: Must be confident, able to work in a team, and a good team player. Should be stable and calm, supporting functional colleagues. The ability to comprehend facts and data to aid decision-making is essential. Respect, effective listening, caring, and compliance with TEVA’s core values are required. Demonstrates timeliness.
  • Interpersonal Skills: Collaborates with the team within the functional area and cross-functional teams. Provides good technical communication locally and contributes to local and/or global project teams. Delivers technical presentations and works with minimal supervision, guiding junior staff and managing individual products independently.

Reports To
Manager/Sr. Manager/Associate Director, Generic R&D.

Link to apply: Apply now

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