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Associate Scientist, Analytical Development

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POST DATE 8/24/2016
END DATE 1/18/2017

Celgene Summit, NJ

Summit, NJ
AJE Ref #
Job Classification
Full Time
Job Type
Company Ref #
Entry Level (0 - 2 years)


br strong Description /strong br P Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture. /P P As part of Celgene's R&D team, this Associate Scientist will develop, validate, and implement analytical methods to assess physical and chemical properties of pharmaceutical materials.  This work is conducted in a highly-collaborative, multi-disciplinary team charged with the overall research & development of our active ingredients, formulated products, and the associated manufacturing processes. The Associate Scientist plays an important role throughout the development of new drug candidates from discovery to commercialization, contributing to the advancement of new therapeutics in the areas of hematology, oncology, inflammation & immunology. /P P STRONG Responsibilities will include, but are not limited to, the following: /STRONG /P P 1) Contributes to the development of priority drug candidates through the development, validation, and implementation of analytical methods involving modern analytical instrumentation including HPLC/UPLC, GC, dissolution, FT-IR, Karl Fischer titrations, etc. /P P 2) Performs testing for development and clinical materials and stability samples in accordance with established methods, specifications and protocols with limited supervision. /P P 3) Knows the fundamentals of analytical methodology and is able to troubleshoot instrumentation and method performance issues of moderate complexity. /P P 4) Documents / reviews laboratory work using laboratory notebooks / worksheets that is detailed, timely and in compliance with GLP / GMP requirements. /P P 5) Contributes to the preparation of high-quality technical reports as source documents for regulatory submissions. /P P 6) Reviews data for compliance to specifications and acceptance criteria. /P P 7) Communicates results according to project timelines and works with collaborators to understand project needs and contribute to overall analytical control strategy.  Draws basic conclusions from data and results. /P P 8) Other duties as assigned by supervisor. /P P *LI-KM1 /P P BIO-US  /P