Regulatory Affairs Specialist
Cedent Life Talent
Job TitleResponsibilities:Determine and document change assessments for US Class II devices to ensure compliance with the US regulation. Plan and prepare submissions for US Class II devices, including creating, translating, revising, reviewing, and compiling documents, as well as responding to questions and requests from the FDA.Determine and document change assessments for EU Class III & IIb devices to ensure compliance with the EU Medical Device Regulation. Plan and prepare submissions for EU Class III & IIb devices, including creating, translating, revising, reviewing, and compiling documents, as well as responding to questions and requests from the Notified Body.Support submission and maintenance of product registrations in markets worldwide.Support product registrations, including creating, revising, reviewing and compiling documents for submission to regulatory authorities, as well as assisting in responding to questions and requests from such authorities.Assist in external audits by supporting responses to auditor questions and requests.Keep abreast of new or changed regulations and standards and perform gap analyses.Perform additional duties as assigned.Qualifications:(REQUIRED) Bachelor's degree, preferably in the life sciences; advanced degree a plus.(REQUIRED) At least 3 years of experience in medical device field, including hands-on experience with submissions.Experience in regulatory submissions to medical device regulatory bodies a plus; e.g., FDA, Health Canada, ANVISA/INMETRO, EU NB, MHRA, Swissmedic, NMPA, PMDA, MFDS, and TGA.Experience with software-driven and electro-mechanical medical devices a plus.Strong knowledge of US and international requirements for regulatory submissions and maintenance of medical devices.Team player with ability to work independently in hybrid/in-person setting (Bedford, MA).Excellent and effective written and verbal communication skills.Excellent interpersonal skills, good judgment and analytical skills.Effective time management and organizational skills.Consistent, quality work and commitment to follow-through.
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- ...Anika-GCC in Bedford, MA is seeking a Regulatory Affairs Specialist II to support regulatory submissions and regulatory authority interactions related to product submissions and approvals. You will prepare and submit regulatory documentation, support product market approval...Suggested
- The Sr. RA Specialist is Responsible for preparation of regulatory submissions (domestic and foreign). Ensure implementation and maintenance of regulatory filing... ...agenciesAssist with other basic Regulatory Affairs functions, such as scanning and archiving records Other...SuggestedLocal area
- Anika is seeking a Regulatory Affairs Specialist II to support regulatory submissions, authority interactions, and post-approval activities. The role requires preparing documentation, maintaining compliance, and guiding cross-functional teams through regulatory processes...Suggested
- ...Position Overview This position is intended to provide Regulatory Affairs support to FUJIFILM Healthcare Americas Corporation. This position supports full, ongoing compliance to all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements...SuggestedLocal areaRemote workFlexible hours
- ...Senior Regulatory Affairs SpecialistBrioHealth Solutions is seeking a skilled and self-motivated Senior Regulatory Affairs Specialist to support the BrioVAD® Left Ventricular Assist System. This individual will partner with cross-functional teams to support product development...
- ...BrioHealth Solutions is seeking a Senior Regulatory Affairs Specialist to support the BrioVAD LVAS. This role partners with clinical, R&D, quality, and medical affairs teams to drive regulatory planning, submissions, and lifecycle management. You will manage FDA submissions...
- Job DescriptionMIT Lincoln Laboratory is a Department of Defense Federally Funded Research and Development Center (FFRDC) engaged in the development and demonstration of advanced prototype technologies and systems, with an overall objective to transfer those capabilities...Contract workWork at office
- Sr. Regulatory Affairs Specialist role at Glaukos Corporation Sr. Regulatory Affairs Specialist (Hybrid - Acton, MA) The Sr. RA Specialist is Responsible for preparation of regulatory submissions (domestic and foreign). Ensure implementation and maintenance of regulatory...Full time
- Glaukos Corporation in Acton, MA, is seeking a Sr. Regulatory Affairs Specialist to lead the preparation of regulatory submissions for the U.S. and international markets. The role is hybrid and full-time, requiring a proactive regulatory mindset and collaboration with cross...Full time
- BRIOHEALTH SOLUTIONS INC, based in Massachusetts, seeks a Senior Regulatory Affairs Specialist to lead FDA submissions and regulatory planning for BrioVAD LVAS. You will partner with cross-functional teams to ensure compliance across US and EU programs, including IDE/PMAs...
- ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the...Immediate start
- ...assess vendor SCAR (Supplier Corrective Action Reports) and ensure effective follow-up.Ensure vendor-supplied products comply with regulatory and quality standards.Develop and maintain strong, long-term relationships with approved vendors.Evaluate new vendor capabilities...
- ...enables us to be a powerful contributor and connector of right Talent. Job Description This individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual...
$101.6k - $131.9k
...tough problems. Job Summary Responsible for supporting regulatory activities regarding released product, including, MDR investigations... ...field required. A minimum of 4 years of direct Regulatory Affairs experience is required, including preparation of Pre-IDEs, 510...Shift work$94k - $150k
Job TitleSenior Regulatory Affairs SpecialistJob DescriptionSenior Regulatory Affairs Specialist, UltrasoundThe Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities to secure timely product clearances. Responsibilities...Full timeWork at officeImmediate startWork visaRelocation package3 days per week$135.3k - $202.9k
...development and career advancement across the globe.Scope: The Regional Regulatory Lead is responsible for the regulatory strategy and execution... ...degree and at least 5 years of regulatory affairs strategy experience in drug development in the US.Demonstrated...Local areaFlexible hours3 days per week- ...Job TitleResponsible for handling complex submissions with minimal supervision. Organizes regulatory information and tracks and controls submissions. Reviews and advises on labeling for compliance with regulatory filings. Reviews product changes for impact on regulatory...Worldwide
$140k - $180k
...including third-party risk, control testing, and audit readiness—while ensuring the organization is prepared for certifications and regulatory requirements. Additionally, you will enhance our security posture through automation, continuous monitoring, and proactive...- MilliporeSigma in Burlington, MA is seeking a Compliance Officer to advise on ABAC, AML, and business ethics across Life Science, Electronics and Enabling Functions. The role covers global and US perspectives, applying the Compliance Management System and guiding risk assessments...Worldwide
- Sun Pharmaceutical Industries, Inc (USA) seeks a Sr. Associate Compliance to provide scientific support for root cause analysis and closure of OOS and OOT investigations and product quality complaints. You will ensure GLP and cGMP compliance and contribute to the Quality...
- Job SummaryThe Manufacturing Operations and Compliance Specialist is responsible for supporting compliance activities within the manufacturing... ...organization to ensure adherence to internal procedures, regulatory requirements, and quality standards. This role partners...
- Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with...Work at office
$135.3k - $202.9k
Scope The Regional Regulatory Lead is responsible for the regulatory strategy and execution for their assigned projects in their region... ...Qualifications Advanced degree and at least 5 years of regulatory affairs strategy experience in drug development in the US....Local area3 days per week- The Interceptor and Sensor Technology Group supports the development of advanced technologies and systems for use in future surveillance, missile defense, and air defense systems. The Group is currently supporting programs in the domains of advanced interceptor and hypersonic...
$120.44k
Posting Description LICENSING AND BUSINESS DEVELOPMENT OFFICER, Technology Licensing Office, is responsible for the commercialization of MIT’s intellectual property (IP) portfolio arising from research and other activities on MIT’s campus. The Licensing Officer manages ...Permanent employmentFull timeWork at officeVisa sponsorship$147.4k
Posting Description SENIOR LICENSING AND BUSINESS DEVELOPMENT OFFICER, Technology Licensing Office, is responsible for the commercialization of MIT’s IP portfolio arising from research and activities on MIT’s campus; managing a large portfolio of cases, including, technology...Full timeWork at officeVisa sponsorship$196k - $270k
...Biogen's US business. Your expertise will ensure that our business operations adhere to the highest standards of compliance and regulatory conduct. By developing and delivering comprehensive training programs, you'll be an educational pillar for both new and established...Full timeTemporary workWork at officeLocal area$88k - $147k
...the FME’s Global Compliance Program, including following all regulatory and division/company policy requirements Responsible for the development... ...with the law department, regulatory and government affairs to better understand operational requirements under the law. Assists...Full timeWork experience placementWork at officeRemote workFlexible hours- MACOM designs and manufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications. Headquartered in Lowell, Massachusetts, MACOM has design centers and sales offices throughout North America, Europe and Asia. MACOM is certified...Work at office
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