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Teva Pharmaceuticals
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Formulation Researcher II

Formulation Researcher II

Teva Pharmaceuticals

3 - 10 years

0 Lacs

maharashtra

Posted:1 day 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

**Job Description:** **Role Overview:** As a Bench Scientist at our company, you will be responsible for conducting experimentation in the area of formulation research and development, process development, regulatory and intellectual property for global markets. You will play a crucial role in planning and executing experiments in line with Quality by Design (QbD) principles, using One Factor at a Time (OFATs) and Design of Experiments (DOE). Your work will involve applying scientific principles of QbD, DoE, statistics, and scale-up principles to products at different stages from selection to launch. Additionally, you will work on understanding intellectual property scenarios, developing strategies, and establishing proof of concepts through experimentation. Your role will also involve identifying challenges and bottlenecks in development, proposing mitigation strategies, and coordinating with cross-functional teams for technology transfer and timely execution of submission batches. **Key Responsibilities:** - Conduct experimentation in line with QbD paradigm, using OFATs and DOE - Work on products at different stages from selection to launch using scientific principles - Comprehend facts and data from literature and present information effectively for decision-making - Understand IP scenario, work on design strategies, and establish proof of concept - Identify challenges and bottlenecks in development, propose mitigation proposals - Coordinate with cross-functional teams for technology transfer and timely execution of submission batches - Prioritize activities for experimentation, participate in development trials, and commercialization - Align activities with established milestones and global operation site requirements - Communicate effectively with internal stakeholders to address challenges and risks - Assist in business process evaluation and identifying improvement areas - Demonstrate personal accountability, effective work habits, and continuous learning **Qualifications Required:** - Ph.D. in Pharmaceutical Sciences with 3+ years of experience or M.Pharm in Pharmaceutical Sciences with 6 to 10 years from reputed universities - Experience working in high-performance teams in the generic pharmaceutical space in regulated markets such as US, EU, or Canada **Additional Details:** The company is on a mission to make good health more affordable and accessible globally. With a diverse workforce across nearly 60 countries, we are the world's leading manufacturer of generic medicines and produce products listed on the World Health Organization's Essential Medicines List. We strive to make a positive impact and are always looking for new ways to innovate and help improve the lives of millions around the world.,

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Teva Pharmaceuticals

Pharmaceutical Manufacturing

Tel-Aviv Petach Tikva

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Formulation Researcher II