Internal Quality Audit Medical Device Jobs in California

IRRAS USA Inc. - San Diego, CA, United States

derived from internal manufacturing results, customer feedback, and device field performance. Leadership over all internal, external, and supplier audit activities. Oversight of quality plans. Manage

from: linkedin.com - 7 days ago

VIDA Connected Specialists - , CA, United States

findings. Skills : Familiarity with process validation (IQ/OQ/PQ), biocompatibility, sterilization, and packaging requirements for medical devices. Strong understanding of GMP regulations and quality

from: linkedin.com - 10 days ago

AbbVie - Dublin, California

through the implementation of inspection criteria, procedures, and training. Perform duties in compliance with FDA’s Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations

from: resume-library.com - 11 days ago

GForce Life Sciences - Fremont, CA, United States

initiatives. Prepares for and leads internal and external audits, manages recertification projects, and drives compliance efforts in collaboration with stakeholders. Contributes to process improvements

from: linkedin.com - 20 days ago

Medical Instrument Development Laboratories, Inc. - San Leandro, CA, United States

quality, ensuring compliance with standards, identifying issues, and recommending solutions. Lead and/or support internal and external audits, including supplier audits. Support manufacturing process

from: linkedin.com - 29 days ago

TopTalentFetch - Hayward, CA, US

/External Quality Audit activities and other key quality initiatives, as appropriate Administers and maintains Quality System records Minimum Qualifications 1-3 years of experience in medical device Quality

from: jobvertise.com - 12 days ago

Sonendo, Inc. - Laguna Hills, CA, United States

Management activities, including the execution of supplier qualifications and supplier audits Ensure compliance with design control procedures Maintain compliance with Quality System procedures and company

from: linkedin.com - 29 days ago

Connect Life Science - San Jose, CA, United States

leader in the field of Medical Devices, equipped with an engineering background and a proactive approach, to spearhead a team of 5 direct reports through the development phase of a new product, working

from: linkedin.com - 15 days ago

Katalyst Healthcares & Life Sciences - Carlsbad, California

regulations, agency guidelines and internal policies to assure compliance. Lead process improvement projects and assessment of quality plans. Support Management during external/internal inspections

from: resume-library.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 - 17 days ago