- Compass Group, North America (Groton, CT)
- …Schedule: Full time schedule, Monday - Friday, 7:00 am - 3:30 pm. + Requirement: GMP / GXP experience preferred. + Work environment - Global GMP clinical ... + We have an opening for a full time LEAD WAREHOUSE ATTENDANT position. + Location: Pfizer Groton B100...manufacturing and clinical studies. + Ensure strict adherence to GMP , quality, safety, and environmental standards. + Oversee … more
- Gilead Sciences, Inc. (Foster City, CA)
- …We empower our leaders to step up, share ideas, listen, learn, and lead . We're welcoming bright, diverse, and imaginative minds; we're nurturing them to foster ... industry standards and expectations. + Work closely with the Business Process Owners, Facilities , and Engineering/IT teams to ensure that the deployment of GxP … more
- Charles River Laboratories (Memphis, TN)
- …industry experience. + Knowledge of manufacturing processes and safety in GMP regulated facilities Pharmaceutical/Medical Device/Biotechnology. + Knowledge in ... Sr. Engineer will have the experience to be functional lead responsible for Validation (CQV) deliverables for the facility,...preferred. + Knowledge of manufacturing processes and safety in GMP regulated facilities . + Efficient in Microsoft(R)… more
- Cambrex High Point (Durham, NC)
- …for drug substance and drug product. * Experience with regulatory agency inspections of GXP facilities . * Experience working with CDMOs. * Flexible mindset to be ... client and departmental objectives in a timely manner. Responsibilities * Lead a Stability Storage-oriented core-team managing critical stability programs. *… more
- AbbVie (North Chicago, IL)
- …development and implementation of systems that assure consistent application. + Lead personnel in the application of Quality Assurance policies, procedures, ... and KPIs. + Minimize Data Integrity errors within a quality system and assure GMP documentation standards. + May be required to prepare and present data during… more
- Takeda Pharmaceuticals (Boston, MA)
- …systems (eg Allen-Bradley PLC, Delta V, BAS, Siemens), cleaning processes, process equipment, facilities and GMP critical support systems is required. + Prior ... to the Validation Maintenance Program for annual requalification of GxP manufacturing equipment used for commercial production, including developing validation… more
- Amgen (Holly Springs, NC)
- …with QA partners while supporting computerized systems validation processes in a GxP environment. Maintain Data Integrity Assessments with the current Amgen and ... Out (IV/ACO) in a fast paced environment. **Ongoing operations:** + Lead and support functional area projects passionate about improving process equipment/utilities/… more
- Amgen (Holly Springs, NC)
- …with QA partners while supporting computerized systems validation processes in a GxP environment. Maintain Data Integrity Assessments with the current Amgen and ... and procedures that affect multiple organizational units. **Ongoing operations:** + Lead and support functional area projects focused on improving process equipment/… more
- Bristol Myers Squibb (Summit, NJ)
- …collaborative relationships outside the immediate organization. The incumbent may be asked to lead small to medium sized projects in their area of responsibility and ... activities are performed. **_Regulatory Responsibilities_** + Maintains all required Corporate, Facilities and EHS training as required. + Adheres to all safety… more
- Bristol Myers Squibb (Summit, NJ)
- …portion of their time on individual work or improvements. The incumbent may lead modifications to work processes or procedures to functional management that impact ... **Shifts Available:** Wednesday - Saturday, 8am - 6pm **Responsibilities:** _Management Responsibilities:_ + Lead a team of up to 10 people including full time and… more