Seeking Director of Clinical Trial Material Manufacturing to provide appropriate resources and oversight to ensure full compliance with current Good Manufacturing Practices; corporate standards, policies, and procedures; operational excellence; continuous improvement; personnel development; and overall leadership.
*** Lead current Good Manufacturing Practices manufacturing of Clinical Trial Material, exploring unique solutions for customers and developing technical expertise of the organization.
*** Design and conduct pre-formulation, formulation development, process development, process optimization, scale-up, and clinical manufacturing, including pre-formulation characterization and formulation development studies.
*** Develop, validate, and document prototypes, trial sample production, and new manufacturing methods.
*** Review and author reports and documents such as product development reports, quality overall summary, master formulas and others.
***Bachelor of Science or higher degree in Pharmaceutical Sciences, Chemistry, or equivalent.
*** 5+ years of drug or formulation development experience in pharmaceutical industry.
Join a company with a long standing history of successful and satisfied employees, generous benefit packages include: medical, dental, and vision coverage; excellent vacation and paid time off; company sponsored training programs, 401(k) with company match, and much more.
Please reference #37567172 when responding.
Education Requirements: BachelorDegree
Minimum Experience Requirements: 5-10 years
Job City Location: Minneapolis
Job State Location: MN
Job Country Location: USA
Salary Range: $120,000 to $160,000
Diedre Moire Corporation, Inc.
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