for strategy development and execution of develop. Day in the life: must be self-sufficient, they'll need to make their own...
Roles & Responsibilities: BS/MS in Science (e.g. Chemistry, Biochemistry, Analytical Chemistry) or Engineering (Chemical or Biochemical) with 5+ total years of experience working in a biologic, vaccine or pharma industry. Experience...
Roles & Responsibilities: Bachelor's degree in science or engineering (MS accepted, PhD is overqualified). Minimum 2+ years in Process Validation within the biotech/pharma industry. Writing and executing process validation document...
Responsibilities: Must have Experience in authoring, reviewing, executing and approving validation documents. Interface with Quality organization and the ability to defend rationale in validation documents. Ability to develop cleaning c...
Roles & Responsibilities Strong working knowledge of Quality System Regulations. Experience leading CAPA (Corrective and Preventive Action) activities. Quality review for documents associate with protocols, functional spec, detail desig...
Responsibilities: Coordinates design review meetings to review all quality aspects of new products. Interfaces with Product Development Engineers to ensure quality considerations during the concept stage. Support Design Control activitie...
Roles & Responsibilities: Bachelor's Degree/Undergraduate Degree in engineering or technical discipline or Master's degree preferred. 10+ Years Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturin...
Roles & Responsibilities: Bachelor's Degree/Undergraduate Degree in engineering or technical discipline or Master's degree preferred. 10+ Years Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturin...
Responsibilities: Provides CMC regulatory support and guidance to project teams for clinical development and post approval changes; defines CMC regulatory submission strategies during development and post approval. Experienced with clini...