- United Therapeutics (Silver Spring, MD)
- …purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of ... dynamic biotech and pharmaceutical environment? As a Senior Validation Engineer or Specialist , Equipment, you'll be a subject matter expert in equipment validation,… more
- BD (Becton, Dickinson and Company) (Columbus, NE)
- …BDM, PS document control system and has the local responsibility for the development , implementation, and improvements of the document system as well as maintaining ... it in compliance with ISO, cGMP , BDM, PS and BDX requirements. Interfaces directly with...focus area: + Brings a high level of manufacturing process and Quality Systems understanding to the review and… more
- Globus Medical, Inc. (Audubon, PA)
- …controlling, and auditing documentation that is required for quality and cGMP compliance. The primary responsibilities of the position include the following: ... **Essential Functions:** + Issues Quality System documents and coordinate the training process + Issues device master record documents (manufacturing process … more
- BD (Becton, Dickinson and Company) (Columbus, NE)
- …and skill acquisition by identifying and eliminating barriers, assessing trainee skill development , and remaining current with new and near-term BD products and ... BD policies. The role will also support the continual development of existing associates through new skill development...at BD. + Assist with Quality System training (eg cGMP , ISO, etc) + Support new associates in transition… more
- Medtronic (CO)
- …and materials, on a global basis. + Stay abreast of training and development industry research, (eg learning theory, motivation theory), and new methods and ... Engineers (including job shadow) and Factory to understand the manufacturing process to develop and maintain technical knowledge, system intricacies, and… more
- Kelly Services (Tarzana, CA)
- …equipment are identified and available in time for manufacturing activities. * Support Process Development (PD) and Manufacturing Sciences & Technology (MSAT) to ... or a BS/BA in a relevant science or engineering discipline. * Understanding of cGMP process and knowledge of CMC regulatory framework for biologics. * Knowledge… more
- Lilly (Indianapolis, IN)
- …**Position Summary:** Reporting to the Supervisor of Manufacturing, the Manufacturing Process Specialist (B4) supports daily production and inspection ... activities, contributes to process improvements, and ensures compliance with cGMP ...quality events and support on-time product release + Support process development , technical transfer, and validation activities… more
- J&J Family of Companies (Raritan, NJ)
- …Function:** Supply Chain Manufacturing **Job Sub** **Function:** Manufacturing Pharmaceutical Process Operations **Job Category:** People Leader **All Job Posting ... support both clinical and commercial requirements in a sterile cGMP environment. Their job duties will be performed within...supervise a specific Processing Manufacturing Unit within the CART process operations (Day 0, Cell Culture, Day 10 or… more
- Sanofi Group (Framingham, MA)
- …cell bank qualification and management. + Strong scientific background in biological process development (mammalian and/or microbial) and/or product analytics. + ... the biotech/ pharmaceutical industry, specifically in R&D and/or MSAT (industrial development ) with manufacturing cGMP considerations, and global CMC projects.… more
- Genentech (South San Francisco, CA)
- …own the strategy and execution across three core pillars:** **Data Governance & Process : Oversee and manage a robust data governance framework for ~30,000+ assets, ... solutions that create tangible value.** **Key Responsibilities** **Team Leadership & Development ** + Lead, coach, motivate and develop a high-performing team of… more