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Job Description
Job Description Summary
The Research Associate is responsible for initiating trials for the formulation of injectable products per the development requirements. This role is also responsible for an array of duties including, but not limited, to writing department documents & reports, initiating stability studies, preparing for filings, maintaining log books, and more as instructed by management.
Job Description
- To Perform formulation development assigned by management.
- To Perform & plan predevelopment/ pre-formulation studies, develop lab trials and stability batches, and optimize formula & manufacturing processes, performing the QbD /DoE based trials.
- Observe established standard operating procedure (SOP), as applicable at the all Endo sites (Labs, production facilities etc.), including laboratory safety.
- Conduct literature searches on APIs, patents, excipients, technologies for the development of formulation & planning formulation strategies along with assessment of QTPP & CQA.
- Prepare and review development reports, study protocols & reports including, but not limited, to stability, scale up, MFR, specifications of formulation, tentative specification for API, raw material, and finished product based on scientific rationale.
Education – M. Pharm./MS.
Experience- 1-3 yrs.
Commitment to Diversity, Equity, and Inclusion:
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person’s unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
