Regulatory Affairs PM Lead — Medical Device Divestiture
SRG
Impellam Group is seeking a Regulatory Affairs Program Manager to lead the divestiture and transfer of regulatory documents to a new global medical device organization. You will drive the Regulatory Separation Plan, coordinate registrations, and manage ownership transfers, amendments, and submissions, ensuring GMP-compliant operations. You will oversee global RA programs, engage with health authorities, and ensure alignment across cross-functional teams. #J-18808-Ljbffr SRG
- Job Title Regulatory Affairs Program Manager Location Raynham, MA OR West Chester, PA OR... ...Manager will be the Project Manager leading the Divestiture / transferring of all Regulatory... ...global pharmaceutical / biotech / medical device organization to a new, global exclusively...Medical deviceContract workLocal area3 days per week
- A leading IT staffing firm is seeking a Regulatory Affairs Manager for a remote opportunity. The role involves ensuring compliance with FDA regulations, leading... ...a Bachelor’s degree, 5+ years of experience in medical device regulatory affairs, and strong leadership skills....Medical deviceRemote job
- ...plans across multiple locations. The ideal candidate will possess a Bachelor's degree, 10+ years of leadership experience in the medical device industry, and strong communication skills. This position requires up to 50% travel and a strong presence on-site in Mansfield....Medical device
$130k - $140k
...Raynham, Massachusetts, with 6-8 years of experience in project management within a regulated manufacturing environment, preferably medical devices. The ideal candidate will have strong communication skills and a background in financial management. This role includes...Medical device- ...and long‑term business sustainability while supporting a complex, global medical device organization. Location DePuy Synthes - Raynham, MA or West Chester, PA or Raritan, NJ. Key Responsibilities Lead supply chain finance strategy, planning, and execution to support...Medical deviceLocal area
- 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 extension) Roles and Responsibility... ...development teams, familiarity with FDA regulations for medical devices, submission experience of 510(k)s, generation of files necessary...Medical device
$178k - $307.05k
Sr. Director, Regulatory Law (DePuy Synthes) Location: Raynham, MA;... ...regulatory law matters affecting medical devices and medical technology... ...actions. Partner with Regulatory Affairs and Quality leadership to... ...clearance or approval. Lead regulatory legal risk assessments...Medical deviceImmediate start- 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
- A professional staffing agency is seeking a Regulatory Affairs Specialist in Mansfield, MA. The ideal candidate will have experience working... ...teams and must be knowledgeable in FDA regulations and medical device submissions. This role involves providing regulatory assessments...Medical device
$117k - $201.25k
...Sub Function Clinical/Medical Operations Job Category... ...bodies, as may be required, regulatory approvals and other... ...designs, develops and leads workshops to define processes... ..., R&D, and Regulatory Affairs Responsible for... ...Experience within the medical device industry and knowledge...Medical deviceLocal areaImmediate start- Dormont Manufacturing Co is looking for a Regulatory Affairs (RA) Specialist in Bridgewater, Massachusetts. This role involves supporting regulatory submissions and compliance to ensure medical device products meet applicable regulatory requirements. The ideal candidate...Medical device
- ...have at least 10 years of finance experience, strong analytical skills, and the ability to lead teams. Expect travel up to 20%. Join us in making a meaningful impact within a global medical device organization. #J-18808-Ljbffr 6149-DePuy Synthes Products Inc. Legal EntityMedical device
- A 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
- 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...Medical device
- 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
- ...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
- ...minimum of a High School Diploma and at least 2 years of manufacturing experience. This position requires strong troubleshooting skills and the ability to work effectively in a team environment. Shifts are from Sunday to Thursday, starting at 12 PM. #J-18808-Ljbffr AptyxMedical deviceShift workNight shift
$20 per hour
3rd Shift Lead Custodian - Sunday to Thursday (10:00 PM - 6:30 AM) Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. To apply for the position, please click the Apply...Hourly payFull timeWork at officeShift workNight shift- ...operating machinery for their commercial or medical operations. Responsibilities include... ...manufacturing experience, preferably in the medical device sector, and possess strong troubleshooting... ...is for the 2nd Shift, Monday to Friday, 4:00 PM - 12:30 AM. #J-18808-Ljbffr AptyxMedical deviceMonday to FridayAfternoon shift
$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... ...regulations. In this role, you will lead the preparation, analysis,... ...which may include device 510(k), IDEs, PMAs) and serving... ...field preferred. 5+ years of medical device regulatory affairs...Medical devicePermanent employmentLocal area
- Responsibilities Lead and evolve EHSS Assurance, Strategy, Standards, and Operational... ..., and governance models aligned with regulatory and internal requirements. Drive... ...Excellence roles within a regulated industry (medical device, pharmaceutical, or healthcare...Medical device
$170k - $230k
...and forecasting across regions. The ideal candidate has over 10 years of experience in finance, preferably within healthcare or medical devices, and possesses strong analytical and leadership skills. An MBA or CPA is preferred. The position offers a competitive salary...Medical device- Spectrum Vascular is an innovative medical device company focused on vascular access and medication management. Our mission is to improve... ...and an entrepreneurial mindset. Role Description The Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory...Medical deviceInternshipWork at officeWorldwide
- ...within Argos Corporation's commercial or medical operations. You'll set up, operate, troubleshoot... ...system (Ex: ISO9001/13485); Medical device industry background preferred. Experience... ...Available shifts 2nd Shift Monday - Friday (4:00 PM - 12:30 AM). Shift ends Saturday Morning....Medical deviceMonday to FridayFlexible hoursShift workDay shiftAfternoon shift
- ...Perm - Remote Opportunity - Regulatory Affairs Manager Established in 1991,... ...regulations. In this role, you will lead the preparation, analysis,... ...which may include device 510(k), IDEs, PMAs) and serving... ...field preferred. 5+ years of medical device regulatory affairs...Medical deviceRemote jobPermanent employmentTemporary workLocal area
$102k - $177.1k
...of Manager of Commercial Operations to lead the Commercial Operations and Sales Support... ...and projects. Experience in the Medical Device industry. Johnson & Johnson announced plans... ...bodies, as may be required, regulatory approvals and other customary conditions...Medical deviceFull timeLocal areaImmediate start$101.5k - $152.25k
...limits off living. Are you a regulatory affairs professional who enjoys working at the... ...a key role in supporting life changing medical technologies used by patients around the... ...strategies for new and modified medical devices Preparing and managing regulatory submissions...Medical deviceLocal areaFlexible hours$102k - $204k
Technology Manager, Quality Systems, AI Lead DePuy Synthes is recruiting for this Technology Manager, Quality Systems, AI Lead position... ...continuous improvement initiatives aligned with business and regulatory requirements Drive the integration of AI and advanced analytics...Local areaImmediate start
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