- ManpowerGroup (South San Francisco, CA)
- … Auditor to lead their auditing activities in South San Fran, CA. **Job Title: Medical Device Senior QA Auditor ** **Location: South San Francisco and San ... degree and at least 6 years of experience + Medical Device manufacturing/Quality experience + Demonstrated knowledge...Documentum platforms Must Haves + **Certified ISO 13485:2015 Lead Auditor , with auditing experience** + **MDSAP auditor … more
- Fujifilm (College Station, TX)
- …**_Minimum Qualifications:_** + Experience working in an auditing role within the Pharmaceutical/ Medical Device industry. + Bachelor's Degree in the Life ... integral member of the Global Supplier Quality Management team, the Supplier Quality Auditor Lead will be responsible for managing and leading the Supplier auditors… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …(SOPs), regulations, standards, good clinical practices, and guidelines applicable to the medical device industry to contribute to overall quality and regulatory ... **12071BR** **Title:** Sr Auditor , Clinical Trials **Job Description:** Provide support to...standards, good clinical practices, and guidelines applicable to the medical device industry. + Identify gaps and… more
- J&J Family of Companies (Cincinnati, OH)
- …application of Good Laboratory Practices (GLP). + Experience working in the Medical Device or Pharmaceutical industry. + Experience leading a cross-functional ... Manager, Quality Assurance (QA) Preclinical Auditor - 2406217771W **Description** Johnson & Johnson MedTech is recruiting a **Manager, Quality Assurance (QA)… more
- Abbott (Chicago, IL)
- …or Quality Management. + Minimum 8 years of related experience in the medical device / pharmaceutical industry. + Knowledge of Good Manufacturing Practices ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Sandia National Laboratories (Albuquerque, NM)
- …state or federal law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, ... of onsite work and working from home) + Generous vacations, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and… more
- Sandia National Laboratories (Albuquerque, NM)
- …state or federal law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, ... work and working from home) + Generous vacations, strong medical and other benefits, competitive 401k, learning opportunities, relocation...Your Job Will Be Like: We are seeking an Auditor , Financial and Business Applications. On any given day,… more
- PCI Pharma Services (Philadelphia, PA)
- …in production, equipment and or process Packaging, Pharmaceutical, Bio-Pharmaceutical, and/or Medical Device background is preferred. LANGUAGE SKILLS: Must ... to pioneer and shape the future of PCI. Job Title: Quality Auditor Department/Group: Quality Location: Philadelphia Reports to: Quality Operations Supervisor FLSA… more
- Kelly Services (Jacksonville, FL)
- …Excel proficiency + Basic computer user skills + Ability to work in a regulated Medical Device business environment. + Punctual and Professional. As part of our ... care manufacturing industry! Look no further than our open positions for Plastic Auditor in Jacksonville, FL. Benefits + Full-time + Shift Differential and Overtime… more
- C&S Wholesale Grocers, Inc. (York, PA)
- …by:** + Conducting accurate cycle counts of inventory locations per handheld device /forms in the warehouse and make system updates as required + Researching ... offer:** + Paid training provided + Weekly Pay + Benefits available from day 1 ( medical , dental, vision, company matched 401k) + PTO and Holiday Pay offered + In… more
- AbbVie (North Chicago, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: Manager, Medical Device Quality Systems is responsible for supporting the ... expertise in both current and emerging regulations and standards impacting AbbVie medical device and combination products. + Performs regulatory compliance… more
- AbbVie (Irvine, CA)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: Manager, Medical Device Quality Systems is responsible for supporting the ... expertise in both current and emerging regulations and standards impacting AbbVie medical device and combination products. + Performs regulatory compliance… more
- Nelnet (Columbus, OH)
- …by an accredited certification body) Audit certifications: + ISACA Certified Information Systems Auditor (CISA) + GIAC Systems and Network Auditor (GSNA) + ... Certified ISO 27001 Lead Auditor or Internal Auditor (when issued by an accredited certification body) + IRCA ISMS Auditor or higher-e.g., Auditor /Lead … more
- Catalent Pharma Solutions (Somerset, NJ)
- …experience, required + Experience working in an auditing role within the Pharmaceutical/ Medical Device industry + Knowledge and understanding of the following ... Supplier Quality Regional Lead will oversee management of the regional Supplier Auditor Team and appraisal processes including routine Goal and Objective discussions… more
- Abbott (Plymouth, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...support and document QMS compliance audits as certified lead auditor or team member. These audits must be tracked… more
- Microsoft Corporation (Atlanta, GA)
- …for clinicians, staff, and patients. We are looking to hire a Senior Medical Device Specialist, with a technical background and a customer-driven passion ... **Responsibilities** We are looking for someone who will bring Medical Device and Regulatory expertise, with a...devices + Regulatory Affairs Certification (RAC) Devices, lead ISO13485 auditor , or equivalent + Experience working with legal /… more
- LSI Solutions (Victor, NY)
- …in 1986, located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive ... passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R)...Review and collaborate on test reports. + Complete internal auditor training and participate on the internal audit team.… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO 14971, ISO 13485,...in a manufacturing environment preferred + One year of auditor experience preferred + Certification as a CQA; CQE… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Abilities (KSAs)** + Demonstrated knowledge in 21 CRF Part 820, ISO 13485:2016, Medical Device Directive / Regulation + Strong computer knowledge (MS Office),… more
- Insight Global (Carlsbad, CA)
- …sciences - Experience in ISO 9001:2015 environment; familiarity with ISO 13485 ( medical device standards) is preferred - Proven experience performing internal ... including the QC Manager and Supervisors, and serve as the internal auditor leading audits. Additionally, they will champion the development of other individuals… more