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Jun
30
Sandeep Singh Dhillon
Vacancy – Pharmaceutical Formulation Development Advisor at UPM Pharmaceuticals – Monster.com
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About the Job

Pharmaceutical Formulation Development Advisor

Bristol, TN 37620

UPM Pharmaceuticals, Inc., (upm-inc.com) a rapidly growing contract drug development and manufacturing company for the pharmaceutical industry, located in Bristol, Tennessee, is seeking two senior advisors/guides for pharmaceutical formulation development.

Essential Duties and Responsibilities: This role requires experienced formulation and process development scientists with project leadership experience in development of pharmaceutical solid oral dosage form products and manufacturing processes. Will provide science & technology guidance in support of client projects in various product development and manufacturing activities within time and budget constraints. Guidance will be provided to all levels within R&D, Manufacturing, Business Development, Quality, and Executive Management. Major activities include: contract proposal review; business development support; technical guidance for project leaders and participation in design of formulations and manufacturing processes; evaluation & implementation of new technology & equipment; attend team meetings; review documents; answer technical questions and participate in discussions; presence on mfg floor or lab during critical operations; write technical reports; advise on procedural, document, and batch record questions; advise registration and validation activities; and many other lesser activities.

Qualifications:

Pharmaceutical formulation development experience is required. Preference for CDMO (contract development and manufacturing operation) experience with solid oral dosage forms and a PhD, but not required.

Academic study of industrial & physical pharmacy, pharmaceutical chemistry, chemical engineering, chemistry, or biochemistry; skill in the science & art of pharmaceutical product development; experience & knowledge of pre-formulation, formulation development, clinical manufacturing, analytical testing, quality control & assurance, cGMP, & GLP; knowledge of programs like Outlook, Word, Excel, Access, TrackWise, and Documentum; knowledge of contract development, concept product development, clinical phase 1, 2, and 3, biobatch, registration, and validation; experienced with IND/NDA/ANDA, QBD, CPP, DOE, and RLD activities; detail oriented, a self-starter, excellent organization & communication skills; ability to handle multiple tasks involving various departments in a fast-paced environment; effective interpersonal skills; ability to read, analyze, interpret, & write scientific documents/reports; the will & ability to achieve success.

Apply at http://job-openings.monster.com/Pharmaceutical-Formulation-Development-Advisor-Bristol-TN-US-UPM-Pharmaceuticals/11/185132690?MESCOID=1900254001001&jobPosition=7



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