Director of Regulatory Affairs - CMC
Global leader in the development and production of life saving pharmaceuticals seeks a Director of Regulatory Affairs - CMC to oversee a large regulatory affairs group working on chemistry and manufacturing controls throughout the company. This highly regarded company offers excellent career growth opportunities across its many divisions, both domestic and international. The Director of Regulatory Affairs - CMC will:
Be responsible for all ANDA ...
Support the development and manufacture of innovative vaccines by leading a team of analytical chemists in the design and implementation of protein characterization methods.
Requires at least 5 years experience managing the development of analytical methods through the use of some, if not all, of these technologies: Isoelectric Focusing, SDS-PAGE, Liquid Chromatography, Mass Spectrometry, Gel Electrophoresis, and Imaged Capillary Electrophoresis
Annually recognized as one of the top vaccine ...
Seeking hands on scientist and team leader to scale up and transfer protein purification processes into clinical and commercial manufacturing.
Shall:
*** Develop extraction methods for proteins derived from E-coli, Yeast and CHO cells
*** Purify Enzymes, MAB’s Cytokines, PEGylated Proteins and Growth Factors
*** Create GMP procedures for scale up, technical transfer, and training of personnel in manufacturing
High growth visible position with top company. Salary $70,000 to $90,000 plus ...
Validation Manager - Pharmaceuticals
Highly regarded, global pharmaceutical leader seeks a Validation Manager to lead a site-wide validation group at the company's flagship manufacturing site in suburban Saint Louis, MO. The Validation Manger will:
Manage validation engineers and teams in all aspects of validation, including all validation activities and systems
Develop, design and execute validation protocols
Review and approve engineering change control, plant validation protocols ...
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