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‑functional... ...in a regulated industry (Medical Device, Pharmaceutical, Nutrition, or Food...Medical deviceHourly pay$100k - $200k
...-site at their Alameda location. This role will focus on regulatory submissions for innovative diabetes management solutions, influencing... ...’s degree in a scientific discipline and experience with medical devices. The position offers a competitive salary of $100,000 - $...Medical device$148.7k - $297.3k
...The Opportunity This Associate Director Regulatory Affairs will work on‑site out of... ...to complete a regulatory submission. Write and edit technical... ...industry (e.g., medical products). ~5-7 years’... ...and Software as a Medical Device (SaMD). ~ Experience with...Medical device- Abbott is seeking a Medical Events Specialist I in Alameda, CA, to manage regulatory reporting for medical device incidents across global authorities. Responsibilities include timely review and submission of medical event reports and collaborating with internal teams....Medical device
- Abbott Laboratories is seeking a Senior Specialist in the Medical Events Group. You will ensure timely review and filing of Medical Device Reports and other regulatory submissions while collaborating with various teams. A Bachelor's Degree and a minimum of 5 years of regulatory...Medical device
$100k - $200k
...Employees can qualify for free medical coverage in our Health... ...Opportunity This Principal Regulatory Affairs Specialist - APAC position will... ...facilitate understanding and secure submission approval. Coordinate with... ..., in vitro diagnostic devices and/or medical devices. Experience...Medical deviceFor contractors$100k - $200k
## Principle Regulatory Affairs Specialist - Diabetes Care (on-site)Applylocations... ...products in diagnostics, medical devices, nutritionals and branded... ...responsibilities for US submissions for new product... ...regulatory agencies and trade associations, develop innovative regulatory...Medical deviceWorldwideShift work$100k - $200k
...can qualify for free medical coverage in our Health... ...Principal International Regulatory Operations Specialist... ...regional RA to update submission strategies and registration... ..., In vitro diagnostic devices and/or medical devices... ...from the Regulatory Affairs Professionals Society)...Medical deviceWorldwideShift work$45 - $50 per hour
...Currently seeking a Clinical Research Associate in Alameda, CA. Details for the... ...training investigators, and preparing submissions. Qualifications: Bachelor... ...side is Required. Experience with medical device or in-vitro device study is Required....Medical device- Experis is seeking a Regulatory Affairs Associate to join their team in Alameda, CA. This role involves ensuring compliance with regulatory standards... ...reviewing labels and promotions, supporting regulatory submissions, and collaborating with various teams. The ideal...Medical device
- ...assurance, and compliance with regulations. The ideal candidate will have a relevant engineering degree and at least 2 years of experience, preferably in medical devices. A generous benefits package and a supportive work environment are offered. #J-18808-Ljbffr Penumbra, Inc.Medical device
- An established industry player is seeking a Regulatory Affairs Specialist with extensive experience in medical devices. This pivotal role involves overseeing complaint handling processes, ensuring compliance with regulatory standards, and actively participating in the...Medical device
- Epia Neuro in Alameda, CA, is seeking an Electrical Systems Engineer II to design and prototype low-power electrical systems for medical devices. This role emphasizes collaborative work across teams to deliver integrated products impacting patient outcomes positively. The...Medical device
$80k - $105k
A leading medical device company in Alameda, California, is seeking a Quality Engineer I to ensure the quality of innovative medical devices. This role involves participating in the design control process, resolving quality assurance issues, and improving manufacturing...Medical device$20.25 - $22.28 per hour
...Our client, a leader in the medical device manufacturing industry, is seeking a Light Assembler... ...manufacturing instructions, SOPs, and regulatory standards such as Federal QSR and ISO... ...Upon completion of waiting period associates are eligible for: Medical and Prescription...Medical deviceHourly payTemporary workMonday to FridayShift work$130.7k - $261.3k
...collaborating in cross-functional teams. Candidates must have a strong background in electrical engineering, particularly with medical devices, and a minimum of 10 years of related experience. Competitive salary range is $130,700.00 – $261,300.00, alongside opportunities...Medical device- ...seeking a Quality Engineer II in Alameda, CA, to manage the quality of medical devices within the Diabetes Care division. You will lead quality-related activities, ensuring compliance with regulatory standards. The ideal candidate has a minimum of 5 years in technical...Medical device
- A global healthcare company is seeking a Senior Quality Engineer to oversee QA processes for innovative medical devices. The ideal candidate will have at least 5 years of experience in quality assurance and a bachelor's degree in engineering. Responsibilities include leading...Medical device
$100k - $200k
...healthcare company is looking for a Principal International Regulatory Operations Specialist to join their Diabetes Care Division in... ...The successful candidate will play a key role in regulatory submissions and compliance strategies for life-changing diabetes products...Medical device$197.3k - $394.7k
...internal functions (R&D, Regulatory, Quality, Operations,... ...development maturity, regulatory submissions and approvals, supply... ...consumer‑focused medical or software products. Associate’s Degree or equivalent experience... ...related to medical devices (e.g., FDA, ISO, QSR...Medical deviceShift work$130.7k - $261.3k
...candidate will lead mechanical design validation, project management, and technical problem-solving in the development of innovative medical devices. The ideal applicant will have over 10 years of relevant experience, a Bachelor’s degree in mechanical engineering or a related...Medical device- ...aligned with the company's clinical, regulatory, and commercialization objectives. The... ...firsthand experience developing and bringing medical devices through PMA pathways, allowing them to... ...pivotal clinical studies, PMA submission, approval, and commercialization readiness...Medical deviceWork at office3 days per week
$130k - $200k
A cutting-edge medical technology company based in California is seeking outstanding electrical engineers passionate about solving neuroscience... ..., testing, and maintaining electronics for innovative medical devices while collaborating across various disciplines. Candidates...Medical device- ...Wealthy & Wise in Alameda, California, is seeking a full-time engineer to design and develop systems for diabetes care management medical devices. The ideal candidate must have a Bachelor's degree in Biomedical Engineering or related field, with at least 4 years of...Medical deviceFull time
- ...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
- ...Laboratories in Alameda, CA is seeking a Senior Regulatory Affairs Specialist to support product development... ...regulatory input on design, preparing submissions, and ensuring compliance for Class II software medical devices. Candidates should have a bachelor's degree...Medical device
$100k - $200k
Abbott is seeking a Principal Regulatory Affairs Specialist to work on-site in Alameda, CA. This role focuses on regulatory... ...have extensive regulatory experience, including submissions for pharmaceutical and medical devices, and should possess strong communication skills. A...Medical device- A pioneering biotech company is seeking an Embedded Software Engineer to design and develop cutting-edge embedded software for medical devices. This role involves collaborating across various engineering teams, optimizing communication systems, and ensuring compliance with...Medical device
$100k - $200k
Abbott is seeking a Principal International Regulatory Operations Specialist to provide regulatory expertise and ensure compliance... ...scientific discipline, and experience in regulatory submissions for medical devices is required. The position offers a salary range of $100,...Medical device$145k - $214k
A global healthcare company is seeking a Quality Engineering Lead to oversee a team dedicated to manufacturing operations of medical devices. In this role, you will be responsible for manufacturing quality performance, and inspection strategy, and ensure compliant production...Medical device
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