Regulatory Affairs Associate: Medical Devices & Submissions
ManpowerGroup Global, Inc.
ManpowerGroup Global, Inc. seeks a Regulatory Affairs Associate in Alameda, CA, to support the Regulatory Affairs team by ensuring compliance and collaborating on regulatory submissions. The ideal candidate holds a Bachelor's degree and has at least 2 years in regulated industries like Medical Devices or Pharmaceuticals. The role involves reviewing promotional materials, developing SOPs, and communicating with cross-functional teams. A focus on regulatory documentation and excellent analytical skills are essential for success in this position. #J-18808-Ljbffr ManpowerGroup Global, Inc.
$40 - $45 per hour
Job Title: Regulatory Affairs Associate Location: Alameda, CA Work Arrangement: 100% Onsite Duration... ...compliance, supporting regulatory submissions, and collaborating with cross-... ...experience in a regulated industry (Medical Device, Pharmaceutical, Nutrition, or Food...Medical deviceHourly pay$90k - $180k
...AlamedaJob Type: Full timeCategory: Regulatory AffairsIndustry:... ...and products in diagnostics, medical devices, nutritionals and branded generic... ..., the Senior Regulatory Affairs Specialist will support product... ...of documentation to support submission activities to meet program...Medical device$100k - $200k
...: Full timeCategory: Regulatory AffairsIndustry: HealthcarePosted... ...in diagnostics, medical devices, nutritionals and... ...global regulatory submissions, which include but not... ...agencies and trade associations, develop innovative regulatory... .../drugs. Regulatory Affairs Certification (RAC)...Medical device$100k - $200k
...and products in diagnostics, medical devices, nutritionals and branded... ...This Principal International Regulatory Operations Specialist will work... ...with regional RA to update submission strategies and registration... ...as RAC from the Regulatory Affairs Professionals Society.) 2-3...Medical deviceWorldwideShift work- ...Alameda, CA, seeks a Senior Specialist in the Medical Events Group to manage timely review, documentation and filing of Medical Device Reports to the FDA, Medical Problem Reports to Health Canada, and related regulatory submissions for the division's products. You will...Medical device
$148.7k - $297.3k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...scientists.The Opportunity This Associate Director Regulatory Affairs will work on-site out of our... ...relevant data to complete a regulatory submission.Write and edit technical documents...Medical deviceWorldwideShift work$81.5k - $141.3k
Abbott is looking for a Medical Events Group Specialist I in Alameda, CA, to manage the documentation and reporting of medical device incidents, ensuring compliance with regulatory authorities. The role requires a Bachelor's degree and at least one year of relevant experience...Medical device- Abbott is hiring a Senior Specialist for the Medical Events Group based in Alameda, CA. This role focuses on managing medical device reports and ensuring compliance with regulatory authority standards. The ideal candidate will have a Bachelor’s Degree in a related field...Medical device
- Abbott in Alameda, CA is seeking a Medical Events Group Specialist (Operations) to ensure... ..., filing and documentation of medical device reports to FDA, Health Canada, EU/EFTA and... ..., and adapt processes to evolving regulatory requirements while delivering high‑quality...Medical device
- ...activities for complex electro-mechanical medical device products within the Product... ...engineering, design, commercial, quality, and regulatory teams Support project study design,... ...and validation in support of regulatory submissions Master of Engineering or related technical...Medical device
- Biomedical Engineer - Medical Device Development (Catheter Systems)Location... ...design, development, and regulatory readiness for novel medical... ...documentation required for regulatory submissions.Support preparation of... ...Assurance/Regulatory Affairs interactions, and a track record...Medical deviceContract work
- Abbott Laboratories in Alameda, CA, is seeking a Principal RA Specialist to lead global regulatory submissions for medical devices and diagnostics throughout the product lifecycle within the Diabetes Care Division. You will provide strategic regulatory leadership, interact...Medical device
$125k - $175k
...multi-disciplinary teams overseeing development of neurovascular devices. Provide engineering support on existing devices for... ...knowledge of quality systems beyond scope. *Develop new processes for medical devices and components *Execute tasks independently and does not...Medical deviceTemporary workWork at officeLocal area- A leading digital health company in Emeryville, CA is seeking a Product Quality Assurance Engineer to ensure compliance with industry regulations and internal standards. This hybrid role involves collaborating with product development teams to drive quality initiatives ...Medical device
$130k
Penumbrainc is seeking a Senior R&D Engineer in Alameda, California, to lead the design and development of innovative medical devices. You will apply your expertise from concept through commercialization, ensuring technical leadership and guidance in developing new designs...Medical device$28 - $31 per hour
...Investigations Tech Our client, a leading organization in the medical device and biotech industry, is seeking a Warehouse - Complaint... ...training will be provided. High School Diploma or GED required; an Associate degree or recent college graduates with a Bachelor's degree...Medical deviceContract workWork at officeShift work- ...engineer for a hybrid role in Alameda, CA. The candidate will design and optimize software for implantable medical devices, ensuring compliance with regulatory standards while having a real impact on therapeutic and diagnostic medicine. The ideal candidate has substantial...Medical device
- ...verification and validation across cloud and mobile platforms within a regulated medical device environment. This role is based in Alameda, CA and focuses on ensuring product quality and regulatory compliance throughout development. You will own end-to-end verification,...Medical device
- EROS Technologies Inc. is looking for a full-time software engineer to design and develop software for safety-critical medical handheld devices. The role involves creating test protocols, performing integration testing, and reviewing requirements. Applicants should have...Medical deviceFull time
$130k - $193k
Penumbra, Inc. in Alameda, CA is seeking a Senior R&D Engineer to design innovative medical devices addressing critical disease states. You will lead projects, create and manage documentation, and work collaboratively across teams. The ideal candidate has a Bachelor's in...Medical device$81.5k - $141.3k
...and products in diagnostics, medical devices, nutritionals and branded... ...countries.Clinical Research Associate IWorking at AbbottAt Abbott... ..., and other applicable regulatory requirements.Participate in... ...preparation of regulatory submissions.May interact with RA/QA in...Medical deviceInterim roleWorldwide- ...adaptive algorithms, and assistive devices to translate neural intent... ...with our Quality and Regulatory teams (including IEC 62304 lifecycle... ...inputs for regulatory submissions. Interface with hardware... ...Experience in regulated medical device software development:...Medical deviceFull timeWork at office
$95k - $127k
...combination of education and experienceAdditional qualifications: Engineering experience in a manufacturing environment recommended, medical device industry preferred Excellent written, verbal, and interpersonal communication skills requiredKnowledge of FDA regulations, Lean...Medical deviceTemporary workWork at officeLocal area$150k - $200k
Full Spectrum in Emeryville, CA, is seeking a Director of Business Development to drive new business within the Medical Device and Life Sciences industries. This client-facing role demands expertise in sales and a strong networking capability, vital for meeting the company...Medical device$50 - $55 per hour
Job Title Clinical Research Associate Location Alameda, CA 94502 Duration 6 months... ...and writing and assembling submissions. Responsible for writing basic study... ...escalate any items needed. Account for devices during study. Prefer medical device background but will accept...Medical deviceHourly payContract workFor contractorsInterim role$150k - $200k
...company in Alameda is seeking an FPGA/Firmware Engineer to architect and develop FPGA-based digital systems for next-generation medical devices. This role demands strong experience in firmware and RTL design, with responsibilities including optimizing designs and...Medical deviceFlexible hours$114k - $228k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...and scientists.The Opportunity This Regulatory Affairs Manager - APAC position will work on-... ...provide support for compiling regulatory submissions, and ensuring data is effectively...Medical deviceShift work$114k - $228k
...businesses and products in diagnostics, medical devices, nutritionals and branded generic... ...with our new sensing technology. This Regulatory Affairs Manager position is an onsite opportunity... ...strategic guidance on FDA pathways, submissions, and interactions, including pre-...Medical deviceShift work$218.7k
...implement quality strategies to align with business objectives and regulatory compliance Monitor and support resolution of on-market... ...technical field 15+ years in Quality or Compliance within the Medical Device Industry or FDA regulated areas Strong communication skills for...Medical deviceVisa sponsorship- ...market globally by leading regulatory strategy across the full product... ...drives highly coordinated submissions and approvals (FDA, CE Mark,... ..., Health Canada, PMDA) for medical device hardware and SaMD products,... ...years of progressive regulatory affairs experience with Class II...Medical device
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