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Teva Pharmaceuticals
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Formulation Researcher II

Formulation Researcher II

Teva Pharmaceuticals

3 - 7 years

0 Lacs

maharashtra

Posted:1 week ago| Platform: Shine logo

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Skills Required

formulation development regulatory intellectual property qbd doe statistics problem solving technology transfer communication skills project management analytical skills quality assurance quality control pharmaceutical sciences bioequivalence gmp glp scaleup principles literature review ip strategy

Work Mode

On-site

Job Type

Full Time

Job Description

As a bench scientist at our organization, you will be responsible for conducting experimentation in the field of formulation research and development for global markets. Your role will involve working with scientific principles such as Quality by Design (QbD), Design of Experiments (DoE), statistics, and scale-up principles. You will be required to analyze data from literature reviews and effectively present information for decision-making purposes. Understanding the Intellectual Property (IP) scenario and working on design strategies, prior art searches, and establishing proof of concept through experiments will be a key part of your responsibilities. You will collaborate with cross-functional teams and coordinate with various departments for technology transfer and timely execution of submission batches. Your problem-solving skills will be put to the test as you identify challenges, bottlenecks in development, and propose mitigation strategies at different stages of the development process. Prioritizing activities, conducting lab experiments, and participating in the execution of development trials will be integral to your day-to-day tasks. Aligning your activities with established milestones, ensuring clear communication with internal stakeholders, and working towards achieving Business Unit Key Performance Indicators (KPIs) are essential aspects of this role. You will also assist in evaluating business processes, identifying areas for improvement, and demonstrating personal accountability and effective work habits. Your day-to-day activities will include working closely with the formulation development teams, conducting experiments in line with QbD principles, preparing presentations at various stages of product development, and conducting literature reviews and experiment designs. You will be responsible for evaluating API & Excipients sources, conducting preformulation studies, executing development trials, and interpreting analytical data for further action plans. Additionally, you will play a crucial role in the execution of Pilot Bioequivalence (BE) batches, scale-up batches, and exhibit batches at different manufacturing locations. Your expertise in establishing stability data, preparing various documents, coordinating with cross-functional teams, and ensuring regulatory compliance will be vital for the successful development and launch of generic drug products. To qualify for this role, you should hold a Ph.D. in Pharmaceutical Sciences with at least 3 years of experience or an M.Pharm in Pharmaceutical Sciences with 6 years of experience from reputed universities. Experience in working with generic products in regulated markets such as the US, EU, or Canada is preferred. Your technical skills should include expertise in Formulation Development of Solid Oral Dosage forms, knowledge of recent ICH and regulatory guidelines, and understanding of Bioequivalence, GMP, Quality, and SOP compliance. Strong people skills, interpersonal skills, and the ability to work both independently and collaboratively with teams are essential for this role. If you are confident, detail-oriented, and passionate about making a difference in the pharmaceutical industry, we invite you to join our team and contribute to our mission of improving global health outcomes through affordable and accessible medicines.,

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Teva Pharmaceuticals

Pharmaceutical Manufacturing

Tel-Aviv Petach Tikva

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Formulation Researcher II