- ThermoFisher Scientific (Greenville, NC)
- …in providing technical leadership and Quality oversight for a Sterile Manufacturing Environment, ensuring compliance with pharmaceutical regulations. This ... **Environmental Conditions** Office **Job Description** **Location/Division Specific Information** The Drug Product Division (DPD) is one of the three divisions… more
- Lilly (Indianapolis, IN)
- …+ Align integrated development plans across key functions ( Drug Substance, Drug Product) and interfaces (device, discovery, manufacturing , quality). + Set ... compliance with all applicable laws, regulations, and industry standards governing drug development. + Provide technical consultation to manufacturing sites… more
- J&J Family of Companies (Malvern, PA)
- …motivated Principal Scientist to join the Biopharmaceutics team within the Drug Product Development and Delivery (DPD&D) organization, focusing on biologics ... biopharmaceutics (monoclonal antibodies, bispecifics, antibody drug conjugates (ADCs), fusion proteins, and other therapeutic proteins). This role will lead… more
- Charles River Laboratories (Wilmington, MA)
- …inside sales, or related experience. Experience in a contract research and/or pharmaceutical setting with knowledge of drug discovery a plus however ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and… more
- System One (East Windsor, NJ)
- …industry, with knowledge of cGMP regulations as they pertain to active pharmaceutical ingredients (API) and sterile finished drug products. Previous experience ... a QA system to notify the US Food and Drug Administration (FDA) of illegitimate products, as and when...for compliance with applicable regulatory requirements and current Good Manufacturing Practice (cGMP) standards prior to release for commercial… more
- Catalent Pharma Solutions (Harmans, MD)
- …of business administration preferred + 10+ years of relevant experience in pharmaceutical or medical device manufacturing , quality or regulatory, general ... management and analysis. + 10+ years of relevant CDMO experience in pharmaceutical , h experience in quality, technical project management, business management and/or… more
- Catalent Pharma Solutions (San Diego, CA)
- …Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Our purpose-built San Diego location provides comprehensive ... Located less than a mile from Catalent's West Coast early-phase oral drug product development center of excellence, customers choosing this convenient Catalent… more
- Catalent Pharma Solutions (San Diego, CA)
- …Diego) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and Our purpose-built San Diego location provides comprehensive ... Located less than a mile from Catalent's West Coast early-phase oral drug product development center of excellence, customers choosing this convenient Catalent… more
- Lilly (Indianapolis, IN)
- …in-process samples, semi-finished and finished products, physical and functional testing of Drug / Device combination product and visual and physical testing of ... and other documents, including amendments. + The monitoring and control of the manufacturing environment. + Plant hygiene. + Process validation. + Training. + The… more
- Catalent Pharma Solutions (Kansas City, MO)
- …onsite** Catalent's Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing , and clinical supply services, supporting a wide ... range of pharmaceutical and biotech products. With cutting-edge technologies and a...+ Bachelor's degree is preferred + Prior experience in manufacturing batch record review highly preferred + Minimum of… more