- Charles River Laboratories (Memphis, TN)
- Senior Validation Engineer Req ID #: 222220 Location: Memphis, TN, US, 38118Memphis, TN, US, 38118 For 75 years, Charles River employees have worked together to ... you build a career that you can feel passionate about. **Job Summary** Sr. Validation Engineer to support our Cell Therapy Manufacturing facility located in… more
- Teva Pharmaceuticals (West Chester, PA)
- …equipment qualification, and GCP, GLP and cGMP regulatory procedures. The Validation Engineer III must have thorough knowledge and experience with global ... Validation Engineer III Date: Apr 16,... Validation Engineer III Date: Apr 16, 2024 Location: West...the development of Validation Master Plans, Cleaning Validation Plans, and Computer Systems Validation… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …manner, and in support of corporate objectives + Act as the quality / validation SME for Change Controls supporting GMP/ GLP systems. + Ensure required Standard ... + Provide quality oversight and support for process, cleaning, shipping, computer system, equipment and instrument qualification and validation activities… more
- Charles River Laboratories (Mattawan, MI)
- Facilities Engineer - MEP Req ID #: 222218 Location: Mattawan, MI, US, 49071 For 75 years, Charles River employees have worked together to assist in the discovery, ... career that you can feel passionate about. **Job Summary** A Facilities Engineer is responsible for coordination, modification, engineering, and design of company… more
- Integra LifeSciences (Boston, MA)
- …and making headway to help improve outcomes. **SUMMARY DESCRIPTION** The Sr. Engineer II, Quality is responsible for providing quality and engineering support to ... new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design &… more
- MD Anderson Cancer Center (Houston, TX)
- …Transplantation and/or Cellular Therapy treatment. **The ideal candidate will have GLP and/or GMP experience.** **KEY FUNCTIONS** 1. **Cell Manipulation and ... processing and documentation requirements for the clinical trial. 1. Utilize various computer systems and databases to enter, retrieve and compile data, complete… more