Regulatory Affairs Manager — Medical Devices, Onsite
CorDx
A multinational biotech organization is seeking a Regulatory Affairs Manager to oversee regulatory documentation for medical device products. You will ensure compliance with FDA and ISO standards, provide regulatory support during product development, and collaborate with cross-functional teams. The ideal candidate has 5-7 years of regulatory affairs experience and a Bachelor's degree. This role offers highly competitive compensation and comprehensive benefits. #J-18808-Ljbffr CorDx
- ...world, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious... ...healthcare. Job Details Job Type: Full time Job Title: Regulatory Affairs Manager Location: Onsite - San Diego, CA Position Summary The Regulatory Affairs...Medical deviceFull timeFlexible hours
- Quality Engineer II — Medical Device (Onsite — Valencia, CA) Possible Contract Extension Valencia... ...providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science... ...Assurance, Operations, Supplier Management, and Medical Safety. Responsibilities...Medical deviceContract workWork at office
- ...partner with Pharmaceutical, Medical Device and Biotechnology clients to... ...expertise in Quality, Regulatory Compliance and Manufacturing... ...applications (i.e. materials management, financial management, HRIS,... ...0 AM - 04:30 PM Work Setup: Onsite in Valencia, CA Pharmavise Corporation...Medical deviceContract workLocal area
- ...Failure Analysis) Location: Onsite - San Diego, CA (will transition... ...failure analysis on returned devices based on user-reported issues... ...in the Global Complaint Management System (GCMS). Identify opportunities... ...role. Experience in the medical device industry. Familiarity...Medical deviceWeekly payPermanent employmentContract workTemporary workWork at office
- ...countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious... ...healthcare. Job Type: Full time Job Title: Associate Regulatory Affairs Manager Location: Onsite - San Diego, CA Position Summary The Associate Regulatory...Medical deviceFull timeWork at officeFlexible hours
- A medical device company is seeking a Supplier Quality Engineer for a 12-month contract. This mid-senior level role involves leading supplier qualification and ensuring compliance with FDA and ISO standards. The engineer will conduct audits, monitor supplier performance...Medical deviceContract work
- ...improvements. Ideal candidates will possess at least a Bachelor's degree in engineering and 5 years of experience in regulated medical device manufacturing. The role requires hands-on experience with process validation and knowledge of FDA regulations. #J-18808-Ljbffr...Medical device
$114k - $228k
Regulatory Affairs Manager - APAC - Diabetes Care (on-site) page is loaded## Regulatory Affairs Manager - APAC - Diabetes Care (on-site)locations... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000...Medical deviceShift work$181.2k - $344.3k
...overseeing compliance with quality systems, leading a team of quality managers, and ensuring effective monitoring of product performance.... ...a Bachelor's degree along with 10 years of experience in medical device quality systems. Key responsibilities include driving CAPA...Medical device- ...calibration, and preventive maintenance on medical equipment. This role ensures regulatory compliance, patient safety, and... ...on a wide range of medical devices, including patient monitors, infusion... ...to established protocols. Manages equipment inventory, preventive maintenance...Medical device
$110k - $150k
Job Description QA & Regulatory Manager - Valencia & Burbank, CA Company Benefits 100% employer paid medical and dental 401(k) matching contribution... ...(DOE) Position is Onsite Company Overview Contributing... .../ ISO 17025, and Medical Device Directive (93/42/EEC) and Medical...Medical deviceWork at office- ...Engineer for their Ventura, California location. In this role, you will lead the design and validation of manufacturing processes for medical devices while ensuring compliance with FDA and ISO standards. Your expertise in process validation and collaboration with R&D will be...Medical device
- A leading recruitment firm is seeking a Regulatory Affairs Manager for their medical device portfolio. The successful candidate will oversee global regulatory submissions, ensure compliance with US FDA and European regulations, and develop regulatory strategies for both...Medical deviceFull time
$25 - $37 per hour
Itlearn360 is seeking a GRC Analyst to work onsite in California. The role involves leading the Information Security GRC team in performing risk assessments, developing security policies, and handling security incidents. A Bachelor’s degree and at least one year of experience...Work at office$25 - $37 per hour
GRC Analyst (onsite) - Mechanics Bank, Irvine, CA (San Joaquin Marsh area). Mechanics Bank values connection, partnership, long-term... ...setting and effectively communicates with all employees and upper management of all levels. Qualifications Bachelor’s Degree in a related...Work experience placementWork at office- A leading medical device firm is looking for a Medical Data Specialist II to design and manage data infrastructure. The ideal candidate will have over 5 years of data engineering... ...is based in Valencia, CA, requiring 3 days onsite per week. #J-18808-Ljbffr Pharmavise...Medical device3 days per week
- Lead Engineering, Regulatory, Quality and Clinical Affairs Recruiter, Medical Device & Diagnostics at BioTalent and Investigo, part of The IN Group Position Summary... ...an experienced and strategic Regulatory Affairs Manager to join our team. This pivotal role will be...Medical deviceFull time
- Supplier Quality Engineer - Medical Device Location: Irvine, CA (Onsite) Duration: 12-Month Contract We are seeking a Supplier Quality Engineer to support... ...works cross-functionally with R&D, Design Assurance, Regulatory, Operations, and Supplier Engineering to ensure...Medical deviceContract work
$135.1k - $225.1k
...functionally with commercial, medical/clinical, regulatory, legal, and HR teams to... ...access strategies. You will manage periodic compliance risk assessments... ...within the medical device or pharmaceutical... ...commercial operations, medical affairs, and other cross‑functional...Medical deviceHome officeFlexible hours$169.6k - $254.4k
About the Role The Senior Manager, Trade Compliance will lead the development and execution... ...Manager partners closely with Legal, Regulatory Affairs, Quality, Tax, Supply Chain,... ...leadership experience. Experience in medical device, pharmaceutical, or regulated healthcare...Medical deviceContract workTemporary workLocal areaWorldwideFlexible hours- ...health issues today and address the medical challenges of tomorrow. We strive to... ...YouTube. Job Description The Director Regulatory Affairs, Device is responsible for combining knowledge... ...and trade associations and provides management with regulatory metrics and information...Medical deviceWorldwide
$148.7k - $297.3k
Position Summary Senior Manager, Forecasting and Strategy - onsite in Alameda, CA, within Abbott Diabetes Care Division. Lead the US forecasting team... ...and verbal communication skills. Experience in medical devices and/or biopharma industry. Deep understanding of healthcare...Medical deviceTemporary work- ...Ziegler Isotope Products is looking for a Quality Assurance & Regulatory Manager to oversee our quality assurance program and compliance with... .... We offer generous company benefits, including comprehensive medical coverage. #J-18808-Ljbffr Downtown Boulder Partnership
$148.7k - $297.3k
The Opportunity This position is an onsite opportunity in the Abbott Diabetes Care Division. As a Senior Manager, Forecasting and Strategy, you will lead and manage... ...verbal communication skills Experience in medical devices and/or biopharma industry with deep understanding...Medical deviceTemporary workWorldwide$121.8k - $174k
...Responsibilities Apply comprehensive medical device engineering knowledge and a thorough understanding... ...studies concisely. Participate in the regulatory submission process as a subject‑matter... ...(FDA, EU MDR). Familiarity with risk management (ISO 14971) and design controls (ISO 1...Medical deviceFull timeWork experience placementLocal areaWork visa$85k - $120k
Why Merit? At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and... ...require notification to regulatory authorities. Liaison between the... ...month after 30 days) Low Cost Onsite Medical Clinic Two (2) Onsite Cafeterias...Medical deviceLocal areaShift workNight shift$120k - $140k
Governance, Risk, and Compliance Manager Responsible for executing... ...management activities, supporting regulatory readiness, maintaining... ...Quality Assurance, Regulatory Affairs, compliance, or GRC within a healthcare or medical device environment. Experience supporting...Medical deviceWork at officeRemote workFlexible hours- ...California seeks an experienced Upstream Product Manager - Connectivity to oversee global product... ...at least 5 years of marketing experience in the medical device industry and proven leadership skills. This fully onsite role offers a chance to work on innovative products...Medical device
- Abbott Laboratories is searching for a Senior Systems Engineer in California to focus on system requirements and oversee interdisciplinary collaboration to enhance system designs. The role involves substantial system engineering practices and technical support to ensure...Medical device
- A growing Medical Device Company in the Northern San Diego County is seeking a highly organized... ...Administrative Department. Below are the details: Onsite M-F in Carlsbad 12+ Month Contract What... ...ACH Resolve invoice discrepancies and manage vendor inquiries with professionalism...Medical deviceContract workWork at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Manager — Medical Devices, Onsite. Be the first to apply!
- quality regulatory manager California, MO
- regulatory affairs director California, MO
- regulatory manager California, MO
- head compliance California, MO
- director global regulatory affairs California, MO
- compliance manager California, MO
- manager regulatory affairs California, MO
- compliance director California, MO
- regulatory affairs manager medical devices California, MO
- senior director regulatory affairs California, MO
