- Charles River Laboratories (Charleston, SC)
- …for process control, batch records, lot number assignment, etc. to ensure compliance with FDA and SOP requirements. * Responsible for maintaining appropriate ... positive healthy workplace, when we are mindful of our compliance standards, and when we choose to do the...efficiencies. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our… more
- Catalent Pharma Solutions (Harmans, MD)
- …coupled with our advanced technologies and collaboration with innovative pharmaceutical , biotech and healthcare companies, will help bring life-enhancing products ... appropriate and proactive client and internal stakeholder communication. + Ensure team compliance with batch records, SOPs and training materials. + Leads by… more
- AbbVie (Mettawa, IL)
- …managing a team of Specialists to ensure excellence in all activities and compliance to policy. The Category Manager is responsible for developing team capabilities ... procurement risk across the relevant category, overseeing process and policy compliance . + Ensure effective project management from initiation to completion,… more
- Astrix Technology (Ridgefield, CT)
- …Added - 30/07/2025 Apply for Job _Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is ... Animal Research Technician **Location:** Fairfield County, CT **Duration:** 1 year contract **Pay rate:** $27-$29/ hr. **Position Summary:** The Animal Research… more
- Catalent Pharma Solutions (Philadelphia, PA)
- **Quality Program Manager** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, ... a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer,...+ Five years of relevant experience working in a pharmaceutical industry or life science industry is required +… more
- Charles River Laboratories (San Diego, CA)
- …the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. Additional ... Monitoring program by correctly identifying unanticipated experimental outcomes and non- compliance events and reporting them appropriately. + Interact with customers… more
- University of Pennsylvania (Philadelphia, PA)
- …committees. + Prepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations (CROs), and required ... study team meetings, research team meetings, and ongoing protocol training/ compliance meetings. + Facilitate the development unit guidance/process documents… more
- Catalent Pharma Solutions (Kansas City, MO)
- …(MS&T) Coordinator** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... is committed to a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer and Catalent employee.** **The… more
- Catalent Pharma Solutions (Kansas City, MO)
- …Human Resources** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... and benefits, employee development and training, organizational development, regulatory compliance to meet the business strategies and customer requirements of… more
- Kelly Services (Lancaster, SC)
- …process control) to ensure product and process compliance . + Oversee compliance activities for contract manufacturers. + Collaborate with other departments ... At least 10 years of experience in Quality roles within the pharmaceutical , nutritional supplement, or similar regulated manufacturing industries. + Prior experience… more