Global Regulatory Affairs Specialist - Medical Devices
Spectrum Vascular
Spectrum Vascular in Bridgewater, Massachusetts is looking for a Regulatory Affairs Specialist to support global regulatory submissions and ensure compliance with medical device regulations. The ideal candidate has a Bachelor's degree in a scientific field and 1-3 years of experience in a regulated environment, particularly with FDA submissions. You will collaborate across teams, prepare regulatory documents, and manage compliance with various standards. This position promotes an entrepreneurial mindset within a thriving team. #J-18808-Ljbffr
- A professional staffing agency is seeking a Regulatory Affairs Specialist in Mansfield, MA. The ideal candidate will have experience working with... ...teams and must be knowledgeable in FDA regulations and medical device submissions. This role involves providing regulatory...Medical device
- Spectrum Vascular is an innovative medical device company focused on vascular access and medication management... ...mindset. Role Description The Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities...Medical deviceInternshipWork at officeWorldwide
- IntePros is seeking a Supply Planning Coordinator for a global medical device organization in Bridgewater, MA. This role involves coordinating inventory planning, maintaining accuracy, and supporting warehouse operations. Ideal candidates have 3-5 years of experience in...Medical device
- ...Job title: Regulatory Affairs Specialist Location: Mansfield, MA Duration: 5+ months (possibility of... ...familiarity with FDA regulations for medical devices, submission experience of 510(k)s, generation... ..., US letter to file (RAD), global regulatory strategy plans (GRSP), collaboration...Medical device
- ...program risks. The ideal candidate has 5-7 years of experience in medical devices or consumer industries, with strong project management skills... ...an opportunity to work with diverse stakeholders and leads global projects while adhering to compliance standards. Candidates...Medical deviceContract work
$101.5k - $152.25k
...limits off living. Are you a regulatory affairs professional who enjoys... ...in supporting life changing medical technologies used by patients... ...to work collaboratively with global teams while shaping... ...for new and modified medical devices Preparing and managing regulatory...Medical deviceLocal areaFlexible hours- ...through Staff Augmentation, Global Talent Management, Value Added... ..., holidays, personal days, Medical, Dental and Vision insurance... ...Insurance. Job Description Regulatory affairs with Technical Files, or equivalent... ...and/or auditing of medical device DHFs, Risk Management files,...Medical devicePermanent employment
$80 - $100 per hour
...$100.00/hr Kelly Science & Clinical is seeking a Regulatory Specialist for our client, a leading medical device company based in Bridgewater, NJ. If you’re passionate... ...to products. Works closely with the Regulatory Affairs labeling group in order to assess and determine...Medical deviceFull timeFixed term contractRemote workMonday to Friday- Regulatory Affairs Manager / Regulatory Affairs Specialist role Established in 1991, Collabera has been a... ...through Staff Augmentation, Global Talent Management,... ...submissions which may include device 510(k), IDEs, PMAs) and... .... 5+ years of medical device regulatory affairs...Medical devicePermanent employmentLocal area
- 6149-DePuy Synthes Products Inc. is looking for a Sr. Director, Regulatory Law to serve as the leading legal advisor on U.S. and global regulatory matters affecting medical devices. The ideal candidate will provide strategic counsel, ensuring compliance with regulatory...Medical device
- Johnson & Johnson MedTech is seeking a Sr. Director, Regulatory Law to oversee global regulatory activities in the orthopaedics medical device sector. You will support regulatory strategy, compliance, and innovation through expert legal counsel and collaboration with various...Medical device
- Smith & Nephew in Mansfield, Massachusetts is seeking a Regulatory Affairs professional to shape regulatory strategy for innovative medical technologies. The role involves developing global regulatory strategies and managing submissions, with a strong focus on compliance...Medical device
- ...Overview The Sr. Source Regulatory Compliance Specialist is responsible for executing... ...with Quality, Regulatory Affairs, Supply Chain, and... ...Preferred Experience in medical devices, healthcare, or other highly... ...Experience working in a global or matrixed organization....Medical deviceContract workLocal area
- ...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
$178k - $307.05k
Position Summary The Sr. Director, Global Benefits COE - Orthopedics provides enterprise... ...with global, regional, and local regulatory requirements and standards. Partner with... ...regulated industries such as healthcare, medical devices, or life sciences. Experience leading transformation...Medical deviceLocal area- ...ownership and leadership for DePuy Synthes’ Global CRM technology platforms, enabling... ...comply with data privacy, security, and regulatory requirements across global markets.... ...Exposure to regulated industries such as medical devices or life sciences. Other Travel: Occasional...Medical device
- Join 6029-MEDICAL DEVICE BUSINESS SERVICES Legal Entity as a Senior Manager of Environmental Compliance in Raynham, Massachusetts. In this role, you will lead environmental compliance programs across sites, ensuring adherence to all regulations while partnering with teams...Medical device
- ...Manufacturing Engineer to support new product introductions in our Global Operations team. You will help design and implement... ...science/engineering and at least 2 years in NPD, plus exposure to medical devices and plastics, will help you succeed. #J-18808-Ljbffr...Medical device
$125k - $175k
...worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-... ...and/or adjudication committees, regulatory submissions, vendor management, and medical... ...closure for full scope regional and global projects, with activities focused on site...Medical deviceRemote jobFull timeContract workTemporary workWork at officeImmediate startWork from homeWorldwide- A global medical device company is seeking a Staff Design & Reliability Assurance Quality Engineer to lead critical risk management activities. This role demands 8 years of experience in a regulated industry, preferably within medical devices, and requires expertise in...Medical device
- ...Ensure adherence to FDA regulations, regulatory requirements, company policies, and operating... ..., and vendors. Background in medical device or other regulated industries. Experience... ...Tolerancing. Willingness to support global projects, including travel....Medical deviceFor contractorsWork at office
$76k - $96.5k
...manufacturing engineering within semiconductor capital equipment, large medical device, or similarly complex electromechanical systems that include... ...to close on Jul 17, 2026. About Actalent Actalent is a global leader in engineering and science services and talent...Medical devicePermanent employmentRelocationShift work- ...communication among diverse groups of stakeholders. Deliver global, multi‑cultural projects using an onsite‑offshore model while... ...Bachelor's degree is required. 5-7 years of experience in the medical devices, consumer, and/or medical device industries. Cross‑functional...Medical device
$62.1k - $85.1k
...compliance activities in accordance with internal procedures and regulatory requirements. Primary responsibilities include supporting... ...years of experience working within a regulated industry (e.g., medical device, pharmaceutical, biotechnology, or similar).* Previous...Medical deviceTemporary work- ...elements within a regulated medical device environment. This... ...in compliance with regulatory and internal... ...Systems, Regulatory Affairs, or a related field required... ...NIPRO Corporation - Global by 2x Inferred from the... ...Quality Document Control Specialist (Cosmetics) - 156698...Medical deviceFull timeWork experience placement
$78k - $117k
...design and manufacture technology that takes the limits off living. Are you passionate about bringing innovative medical devices to life? Join our Global Operations Advanced Manufacturing Engineering team and play a critical role in launching new Sports Medicine...Medical deviceFlexible hours- ...Control Coordinator in Mansfield, MA to manage the document control program ensuring compliance with domestic and international medical device regulations. You will coordinate, process, and maintain controlled documents and training records within the QMS, supporting...Medical device
- ...Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions... ...while maintaining the complex service level expectations. Our global presence with offices in USA (NJ, PA, IL, CA) and offices in...Medical device
- Job Title Regulatory Affairs Program Manager Location Raynham, MA OR West Chester, PA OR Palm Beach Gardens, FL Hybrid... ...of all Regulatory documents from the large global pharmaceutical / biotech / medical device organization to a new, global exclusively Medical...Medical deviceContract workLocal area3 days per week
$95k - $130k
...research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and... ...) or Data Safety Monitoring Board (DSMB), medical writing, regulatory submissions and other study-specific services. Interfaces with...Medical deviceContract workTemporary workWork at officeRemote workWork from homeWorldwide
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