Internal Quality Audit Medical Device Jobs

Planet Pharma - Miami Lakes, FL, United States

Managed the PPAP activities Nice To Have: Certifications: ISO 13485 Lead Auditor Familiarity with medical device regulations and good manufacturing practices Manage Supplier Change Requests Previous SQE

from: linkedin.com - 14 days ago

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

from: linkedin.com - 3 days ago

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

from: linkedin.com - 7 days ago

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

from: linkedin.com - 7 days ago

Intelliswift Software - Fremont, CA, United States

occurrence rankings based on field data as required • Provide input, feedback and data for Quality report outs, Management Review, etc. • Support internal and external audits (FDA, ISO, MDSAP etc.) Minimum

from: linkedin.com - 9 days ago

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

from: linkedin.com - 9 days ago

SHL Medical - , SC, United States

documentation package Conducts internal and supports external audits as assigned to ensure compliance to company quality systems requirements. Additional Responsibilities may Include: Support Material Review

from: linkedin.com - 11 days ago

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

from: linkedin.com - 12 days ago

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

from: linkedin.com - 10 days ago

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

from: linkedin.com - 14 days ago