Regulatory Affairs Pro - Medical Devices & IVDs (Hybrid)
Siemens Healthineers in
Siemens Healthineers seeks a Regulatory Affairs Professional (Finance) in Walpole, MA for a hybrid role. You will prepare/regulatory submissions for FDA/IVDR, support life-cycle documentation, and advise design control and product development teams. Lead technical files, maintain QMS compliance, and collaborate on quality guidelines. Strong regulatory knowledge and cross-functional teamwork are essential for success. #J-18808-Ljbffr Siemens Healthineers in
- Siemens Healthineers AG is looking for a Regulatory Affairs Professional to join their team in Walpole, MA. This hybrid position entails preparing and maintaining... ...and at least 2 years of experience in IVDs or medical devices. Strong knowledge of US/EU regulations and...Medical device
$147.76k - $203.17k
Regulatory Affairs Professional page is loaded## Regulatory Affairs Professionalremote... ...in their career.**This is a hybrid role based in Walpole, MA.****As... ...regulations and standards applicable to medical device market clearance.* Knowledge of IVD products and applicable...Medical deviceTemporary workWork at officeLocal area- Siemens Healthineers in the United States is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions and lifecycle documentation for medical devices and IVDs. You will serve as a regulatory expert, guide design control activities, and collaborate with...Medical deviceRemote job
$122.25k - $176.58k
Job title: GRA Device Associate - Medical Devices and Combination Products (Senior... ...About the JobThe Global Regulatory Affairs (GRA) Device team is a... ...and in-vitro diagnostic (IVD) products within the Sanofi... ...by law.#GD-SA#LI-SA#vhd#LI-HybridPursue progress, discover...Medical deviceFull timeLocal areaWorldwide- AliMed, a leading medical products manufacturer and distributor, seeks a Technical Product Manager (Marketing) - Digital to bridge product expertise with digital content strategy. This hybrid role sits at our Dedham, MA office and partners with Digital Marketing, eCommerce...Medical deviceWork at office
- ...Technical Product Manager (Marketing) - Digital to bridge product knowledge with digital content strategy for our non-core portfolio. This hybrid role is based in Dedham, MA, with two on-site days per week. You will collaborate with Digital Marketing, eCommerce and Product...Medical device2 days per week
$176.92k - $196.58k
...Transmission System Planning’s compliance activities and regulatory filings as required by national, regional and local standards... ...:Professional Engineer’s License preferred.#LI-ES3#LI-Hybrid#engajdCompetencies:Build trusting relationshipsManage and develop peopleFoster...Full timeH1bLocal area- A leading IT staffing firm is seeking a Regulatory Affairs Manager for a remote opportunity. The role involves ensuring compliance with FDA... ...need a Bachelor’s degree, 5+ years of experience in medical device regulatory affairs, and strong leadership skills. This position...Medical deviceRemote job
- A leading IT staffing firm in Massachusetts is seeking an experienced Regulatory Affairs Manager to ensure compliance with FDA and other regulations for medical devices. This role requires a minimum of 5 years in regulatory affairs, including experience with 510(k) submissions...Medical devicePermanent employment
$110k - $130k
...higher in Engineering or the technical sciences7 plus years Medical Device/IVD Experience as a Quality Engineer, or 4+ as a Senior Quality Engineer... ...subsidized cafeteria in our Waltham, MA officeWork Location: Hybrid work schedule on-site in Norwood, MA, 4 days/week on-...Medical deviceWork at officeFlexible hours$169.58k - $233.18k
...cross-functional leadership across R&D, Marketing, Quality, Regulatory Affairs, Manufacturing, Supply Chain, Service, and Operations to... ...Informatics product development programs within a global, regulated medical device environment from program initiation through...Medical deviceTemporary workWork at officeLocal area- ...auditors to ensure strong controls and accurate reporting. The role requires a Bachelor’s degree in finance or accounting and 3+ years in finance or employee benefits. Strong communication and PC skills are essential in a hybrid work environment. #J-18808-Ljbffr Eversource
- Cardinal Health is seeking a Principal Regulatory Affairs Specialist to support the Medical Solutions Regulatory affairs team. They are responsible for regulatory activities associated with new product development and maintenance of business projects. This includes being...Medical device
- ...leading IT staffing firm in Mansfield, Massachusetts is seeking a professional for a role in regulatory affairs. The candidate will be responsible for preparing and auditing medical device DHFs and risk management files while ensuring compliance with US and international...Medical device
- ...Location: Hartford CT, Manchester, NH, Westwood, MA or Berlin CT (Hybrid) The Manager of Distribution System and DER Planning in... ...our customers. The role requires active leadership in ongoing regulatory proceedings – to drive changes necessary for successful implementation...Full timeContract workLocal area
$120k - $180k
...patients first — developing innovative medical technologies that improve the lives of... ...impact.A Day in the LifeThe Principal Regulatory Affairs Specialist will play a key role in launching... ...worldwide for Wound Management devices. Sustaining regulatory responsibilities...Medical deviceFull timeH1bWork at officeLocal areaImmediate startWorldwideFlexible hours- Regulatory Affairs Manager / Regulatory Affairs Specialist role Established in 1991, Collabera has... ...and FDA submissions which may include device 510(k), IDEs, PMAs) and serving as regulatory... ...field preferred. 5+ years of medical device regulatory affairs experience....Medical devicePermanent employmentLocal area
- ...paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K... ...Disability Insurance. Job Description Regulatory affairs with Technical Files, or equivalent in... ...preparation, review, and/or auditing of medical device DHFs, Risk Management files, and/or DMR...Medical devicePermanent employment
- ...and Legal with external partners. Requirements include a finance/accounting background and 3+ years in benefits. The role emphasizes strong communication, data reconciliation, and cross‑functional collaboration in a hybrid work setting. #J-18808-Ljbffr Eversource Energy
- Jobot in Norwood, MA is seeking a Senior Tax Accountant for a hybrid role. You will prepare and review corporate tax returns, conduct reviews, and develop tax strategies to optimize savings while ensuring compliance with federal, state, and local regulations. The ideal...Local area
$176.93k - $196.59k
...inclusive work environment in which team members collaborate to provide our customers with safe, reliable and cost-effective service.HYBRID WORK POLICYEversource supports work-life balance by offering hybrid schedules for certain roles. Eligibility is based on job...Full timeContract workH1bWork at officeRemote work- Temp to Perm - Remote Opportunity - Regulatory Affairs Manager Established in 1991, Collabera has... ...and FDA submissions which may include device 510(k), IDEs, PMAs) and serving as regulatory... ...field preferred. 5+ years of medical device regulatory affairs experience....Medical deviceRemote jobPermanent employmentTemporary workLocal area
$109.25k - $149.5k
...facilities and a diverse portfolio of leading medical devices. Ensure that the corporate audit policy... ...global policies and procedures and the regulatory and legislator requirements are being... ...Quality, Supply Chain, Regulatory Affairs, Product Development, and business leaders...Medical deviceFull timeTemporary workWork experience placement- ...process understanding, address lifecycle management and sustaining engineering changes, and ensure compliance with GMP, ISO, and regulatory standards. This role collaborates across functions to improve yield, reduce scrap, and drive cost improvements through data-driven...Medical device
- SharkNinja in Needham, MA is seeking a Senior Medical Device Compliance Engineer to own design controls and post-market sustaining activities... ...across its Medical Devices portfolio. You will ensure global regulatory compliance, lead DHF reviews, risk management, and ECN...Medical deviceOverseas
- ...cost while ensuring compliance with GMP, ISO standards, and regulatory requirements. The role requires a Bachelor’s degree in engineering... ...3 years in manufacturing engineering, preferably in the medical device sector, with strong problem-solving and #J-18808-Ljbffr INTEGRA...Medical device
- ...for an Actuarial Analyst to join their team, focusing on deliverables for management reporting and annual financial planning. This hybrid position allows flexibility to work from either the Wellesley, MA or Hartford, CA office. The successful candidate will play a pivotal...Work at office
- Cardinal Health is seeking a Senior R&D Engineer to drive innovative medical products from concept through launch, ensuring compliance with... ..., and collaborate with marketing, manufacturing, sourcing, regulatory, and clinical teams to deliver robust product development. The...Medical device
- SharkNinja is seeking a Senior Medical Device Compliance Engineer in Needham, MA to lead design controls and post‑market compliance across medical devices. This hands‑on role collaborates with Engineering, Legal, Program Management and Quality to ensure safe, compliant...Medical deviceOverseas
- Ingenyx, a medical device developer, seeks a Sr. Engineer, Development to lead and oversee development projects for sutures and related devices... ..., and collaborate across functions to ensure quality, regulatory compliance, and customer satisfaction. Applicants should have...Medical device
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