- Cook Medical (Bloomington, IN)
- …CO-OPs* Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements* Must ... Overview The Quality Engineering CO-OP at Cook Inc is a...New Technology Support and Development/ Process Control; Process Validation; Quality Engineering; Project Engineering; Systems Support: Research and Technical… more
- Compass Group, North America (Boston, MA)
- …Management Company-dedicated to Achieving Leadership in the Foodservice Industry-as a Quality Assurance Manager. We are seeking a safety-focused leader with an ... You will oversee the development and maintenance of all Food Safety and Quality Assurance programs, ensuring strictly compliant operations that meet FDA , USDA,… more
- Bausch + Lomb (Greenville, SC)
- …management electronic system (D2-GDMS) and ensures content of site documents meet regulatory and QMS requirements. This position is also responsible for the records ... This position will also routinely provide administrative support for External audits ( FDA , ISO, Global, etc.) when needed. **Key Activities:** + Process Greenville… more
- GE HealthCare (Cleveland, OH)
- …Demonstrated understanding of Medical Device Quality Management System requirements and regulatory requirements, including but not limited to FDA CFR 21 820, ... of the NPI core team, you will ensure adherence to the MIM/GE HealthCare Quality Management System and regulatory requirements, including 21 CFR 820, ISO 13485,… more
- Actalent (Camarillo, CA)
- …ensuring all programs and documentation meet rigorous quality standards and regulatory guidelines, such as FDA and ISO requirements. Lead and participate ... GD&T, prototype, r&D, test method, root cause analysis, 14971, blueprints, euMDR, regulatory audits, FDA , Lean, six sigma, industrial design, bone terminology,… more
- J&J Family of Companies (Santa Clara, CA)
- …+ Working knowledge of cGMP, FDA 820 QSR and ISO 13485 or other Quality Systems + The ability to understand and follow QMS Procedures (eg, SOP and Test Methods) ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Customer/Commercial Quality **Job Category:**… more
- Actalent (Alameda, CA)
- …GxP processes related to managing vendors, partners, and suppliers. + Familiarity with FDA Quality System Regulations and Pharmaceutical guidelines, 21 CFR Part ... commercialization. + Develop and maintain standardized templates based on regulatory requirements. + Conduct follow-up activities with internal stakeholders related… more
- Mentor Technical Group (Juncos, PR)
- …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... Mexico, Germany, Canada, and South America. Responsibilities: + Expertise in Quality Systems such as Deviations (Non-conformities, CAPA, and Change Control). +… more
- Stryker (Franklin, TN)
- …Monitor and maintain adequate quantities of laboratory supplies. + Assist the Quality Control team with technical evaluations of non-conforming test results and ... of recent and applicable industry experience, preferably in a pharmaceutical quality control laboratory + Advanced technical knowledge of analytical methods and… more
- Curia (Camarillo, CA)
- Quality Control Analyst II in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control Analyst II is responsible ... data summaries to management * Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry * Collaborate with… more