98 Internal Quality Audit Medical Device Jobs - page 5
-
Senior Quality Assurance Manager Top Quality Recruitment (TQR) - , NJ, United States and SOPs. Support Internal Audit program and regulatory audits. Preferred Skills Strong interpersonal and written/verbal communication skills Ability to handle multiple priorities daily while being flexible 8 days ago
-
Internal Quality Auditor Ursus, Inc. - Alameda, California and process improvements Performs other related duties and responsibilities, as assigned Qualifications: 4+ years of medical device (class II and III) industry experience 2+ years' experience in quality system 2 days ago
-
Senior Regulatory Affairs Specialist Barrington James - , CA, United States to post market. Support internal and external audits. Requirements: Proven experience in Regulatory Affairs within the medical device industry, with expertise in 510(k) submissions and MDR compliance 12 days ago
-
Senior Quality Assurance Manager Sheathing Technologies, Inc - Morgan Hill, CA, United States you will be responsible for: · Maintaining the company’s Quality Management System (QMS) · Enforce compliance with global regulatory requirements, including 21 CFR Part 820, ISO 13485, ISO 14971, UK Medical Device 12 days ago
-
Associate Specialist- Post Market Regulatory Affairs Applied Medical - Rancho Santa Margarita, California is a key requirement for this role. Position Description: As an Associate Specialist in Post-market Regulatory Affairs, plays a crucial role in ensuring that our medical devices continue to meet regulatory 3 days ago
-
Senior Manager Regulatory Affairs Barrington James - , MN, United States Representing the Regulatory Affairs department in interactions Quality, R&D, Commercial and other departments Minimum qualifications include: 8+ years experience in Regulatory Affairs in the Medical Device 14 days ago
-
Quality Assurance Specialist Certified Laboratories, Inc. - Burbank, CA, United States regulated industry, preferably in pharmaceuticals, medical devices, or biotechnology. · Strong understanding of FDA regulations and guidelines, including cGMP, 21 CFR Part 11, and ICH guidelines. · Proven 17 days ago
-
QA/RA Associate Zeiss Group - White Plains, NY document control process and updates QMS database * Administers Corrective Action/ Preventive Action System * Administers internal audit plan and scheduling * Prepares graphs or charts of data 3 days ago
-
Clinical Research Engineer huMannity Medtec - Santa Clarita, CA, United States products. Drive investigator meetings, Steering Committees Meetings, Events Adjudication Committees and DSMB meetings. Conduct remote study monitoring and internal study audits. Skills, Education 19 days ago
-
Senior/Principal Quality & Design Control Engineer Autonomous Medical Devices Incorp - Santa Ana, CA, United States Required for Position Bachelor's degree in engineering, science or related field required; Advanced degree preferred. A minimum of 7 years of Quality experience in medical device industry, with at least 2 15 days ago
Top locations
- Carlsbad, CA (5)
- Marlborough, MA (5)
- Cambridge, MA (4)
- Minneapolis, MN (4)
- San Diego, CA (3)
- Westborough, MA (3)
- Racine, WI (3)
- Laguna Hills, CA (2)
- See more