- 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
- ThermoFisher Scientific (St. Louis, MO)
- …science-related field. **Experience** + 5+ years related work experience (manufacturing, process development , or quality assurance) in biotech or pharmaceutical ... growth and learning in a culture that empowers your development . With revenues of more than $40 billion and...of all findings. + Drive improvements to the investigation process . + Present investigations to regulatory inspectors, internal auditors,… more
- Bristol Myers Squibb (Summit, NJ)
- …revisions of technical documentation content (eg, investigations, changes, SOPs, and process -related). + Support Technical Product Team, Validation, Development , ... team members. Manufacturing Systems Engineers primarily work with local (site) Business Process Owners, Global MS&T, Global IT, Cell Therapy Network subject matter… more
- Cambrex High Point (Charles City, IA)
- …Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development ... with available systems and software. This position requires a process driven mindset with a process -improvement attitude....Appropriate understanding of regulations in all pertinent areas - cGMP , DOT, IATA, FDA, DEA, EPA, etc. + Key… more
- Pfizer (Parsippany, NJ)
- …of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, ... + Maintain data integrity and ensure compliance with company SOPs, GLP and cGMP regulations. + Train, guide and mentor laboratory technicians, fostering skill … more
- Merck (West Point, PA)
- …solutions that will support business objectives and ensure continuity and cGMP , Safety, and Environmental compliance. They will troubleshoot and solve problems ... develop project scope and guide the projects through the capital management process and project execution/closure. + Partner with Facilities Managers and Maintenance… more
- Novo Nordisk (Petersburg, VA)
- …to advance our capabilities in Emerging Technologies (ET) within Chemical API development and production. The highly experienced site is designed to strengthen and ... activities associated with changes to existing & new systems. Process equipment supported includes propagation, fermenters, media sterilizers and supporting… more
- CSL Plasma (Mobile, AL)
- …operational quality management + Collaborate with center management in the development and implementation of continuous improvement plans + Collaborate with ... correcting or improving operational or quality issues. + Conduct periodic process assessments to ensure compliance of CSL written procedures. Initiate investigation… more
- Medtronic (Lafayette, 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
- Fujifilm (Research Triangle Park, NC)
- …the laboratory operations. **Job Description** Responsibilities: + As a highly skilled specialist , contributes to the development of concepts and techniques. ... maintains inspection readiness, data integrity, and Current Good Manufacturing Practice ( CGMP ) compliance. + Partners with management for technical services, such as… more