- Jabil (Cayey, PR)
- …targets for product quality, customer delivery and cost whilst ensuring a safe and cGMP compliant work environment at all times.. Deploy, promote and lead the use of ... Lead the team in achieving a compliant culture with respect to EHS, cGMP , inventory control and Quality System requirements.. Promote Jabil's values and behaviors..… more
- Fujifilm (Research Triangle Park, NC)
- …activities while maintaining strict adherence to Current Good Manufacturing Practice ( CGMP ), quality and regulatory standards. Flexibility with working hours and ... right place for you. From our Bioprocess Innovation Center to our cGMP -compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether… more
- Eurofins US Network (Columbia, MO)
- …department. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, ELISAs, and ... biology and 5 years of experience working in a cGMP laboratory OR Master's degree and 3 years of...degree and 3 years of experience working in a cGMP laboratory OR PhD and minimum 1 year(s) of… more
- Kelly Services (Barceloneta, PR)
- …control cleaning procedures that comply with current Good Manufacturing Practices cGMP and regulatory guidelines, which include documentation of work procedures ... cross-contamination cleaning methods in areas that require microbial control. + Complete cGMP documentation of training or cleaning performed on paper and electronic… more
- Lilly (Lebanon, IN)
- …and implement the necessary systems and business processes required to support cGMP operations, and build the site culture. This will require significant ... creativity and resilience as the site grows to a full-scale cGMP manufacturing through start up. **Key** **Responsibilities:** **Startup Phase:** + Support… more
- Eurofins US Network (Columbia, MO)
- …department. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, ELISAs, and ... biology and 5 years of experience working in a cGMP laboratory OR Master's degree and 3 years of...degree and 3 years of experience working in a cGMP laboratory OR PhD and minimum 1 year(s) of… more
- Cambrex High Point (Charles City, IA)
- …and subject-matter expertise for analytical data review activities within a cGMP Quality Control laboratory supporting API and intermediate manufacturing. This role ... effective CAPA implementation within TrackWise. + Maintain and manage cGMP -compliant laboratory documentation systems, including instrument logbooks, laboratory notebooks,… more
- Bristol Myers Squibb (Devens, MA)
- …ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP . The Manager, Shop Floor Quality Assurance, Cell Therapy is responsible ... accordance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP . Functional responsibilities include ensuring operational compliance with applicable… more
- Cambrex High Point (Charles City, IA)
- …of OOS, deviations, investigations, and CAPA activities in compliance with cGMP requirements. Key responsibilities include leading supplier and internal audits, ... Laboratory and Operations notebook issuance, ensuring compliance with data integrity and cGMP requirements. + Act as a primary QA contact for customers, internal… more
- Cardinal Health (East Hartford, CT)
- …day. Work hours may be subject to change. **Accountabilities** + Handles CGMP documentation review related to product release, facilities and equipment, material ... the site manufactures products to meet the requirements of 21 CFR 212 ( CGMP ) + Handles and ensures quality of documentation (control, retention, and archival) to… more