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.
- ...Regulatory Affairs Specialist IIThe Regulatory Affairs Specialist II supports regulatory submissions and regulatory authority interactions related to product submissions and approvals. In this role, you will prepare and submit regulatory documentation, support product...Suggested
- ...Senior/Principal Regulatory Affairs SpecialistBrioHealth Solutions is seeking a skilled and self-motivated Senior/Principal Regulatory Affairs Specialist to support the BrioVAD® Left Ventricular Assist System. This individual will partner with cross-functional teams to...Suggested
$150k - $180k
...Overview Position Summary: This position is responsible for ensuring that pre‑market and/or post‑market regulatory activities for digital health products follow applicable domestic and international regulations and guidance. Working independently, with guidance...Suggested- ...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...SuggestedImmediate start
$110k - $130k
...a motivated, detail-oriented, and proactive Senior Compliance Specialist to join our dynamic in-house legal and compliance team! This versatile... ...our Compliance & Ethics, Financial Crime Risk Management, and Regulatory programs. We are looking for an upbeat self-starter who is...SuggestedWork at officeFlexible hours3 days per week$91.7k - $137.53k
Job SummaryThe Senior Regulatory Affairs Specialist will lead activities which support both domestic and international regulatory registrations and submissions activities including working with Marketing, New Product Development, Manufacturing and Engineering. Responsibilities...Full timeWork at office$132k - $198k
...FedRAMP authorization, lead technical control design and documentation, and manage third-party risk management (TPRM).The GCO oversees regulatory, governance, certification, and third-party risk assurance across Mimecast's multi-jurisdictional SaaS security business. You'll...Full timeWork at officeLocal area$135.3k - $202.9k
...presenting great opportunities for personal development and career advancement across the globe.Scope: The Associate Director, Global Regulatory Affairs Lead is responsible for the regulatory strategy and execution for their assigned projects in their region / country....Local areaRemote workMonday to FridayFlexible hours- ...and professional development. Summary of the Role We are looking for an experienced and dynamic Permitting & Regulatory Compliance Specialist II to join our growing team. In this role you will independently manage a defined caseload of permitting and compliance...Work at officeImmediate startRemote workFlexible hours
- What You’ll DoAs the QA Compliance Specialist, you’ll help ensure Anika’s manufacturing operations meet applicable quality, regulatory, and documentation requirements. Working in a regulated medical device and life sciences manufacturing environment, you’ll review production...Full timeInternshipWork at officeImmediate start
- What You’ll DoThe Regulatory Affairs Project Manager/Sr. Manager leads and coordinates cross-functional regulatory programs supporting pharmaceutical, biotechnology, and medical device products. In this role, you serve as the regulatory project management lead for complex...Full timeImmediate start
- ...The role involves Trackwise eQMS management, cross-functional collaboration, and ensuring timely QA closure of investigations. The position requires strong communication, organizational skills, and experience with regulatory/compliance in parenteral #J-18808-Ljbffr
- 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...
$91.75k - $129.6k
Cabot Corporation (NYSE: CBT) is a leading global specialty chemicals and performance materials company headquartered in Boston, Massachusetts, USA.Our businesses deliver a broad range of products and solutions to customers in every corner of the globe, serving the transportation...Full timeWork at officeRemote workWork from homeMonday to FridayFlexible hours2 days per week3 days per week- ...MIT FCU is seeking a Loan Administration Specialist to support nationwide real estate and consumer loan portfolios. You will protect collateral... ...completed on time. The role requires accurate work within regulatory, investor, vendor, and MIT FCU requirements, with attention to...
- 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
- ...This candidate will process all documents from start to finish-and will be doing document training support for the PD group Not a regulatory submissions role! Not technical writing role! Additional Information Candidate Must have: Documentation Processing Experience...Permanent employmentFull timeTemporary workWork experience placementInternship
$140k - $180k
...to frameworks such as SOC 2, ISO 27001, NIST, and GDPR.Define and implement security policies, standards, and controls that meet regulatory and business requirements.Risk Management & AuditsLead risk management efforts, including third-party risk assessments, control testing...$110k - $130k
Retirement Senior Actuarial AssociatePension and other retirement plans have enormous financial implications for employers. Actuaries within Retirement Consulting work directly with our clients' management teams to assess the short and long-term costs associated with these...Full timeTemporary workPart timeLocal area$162.9k - $247.6k
The Wellness Pet Company is on a mission. Every day, we strive to make the best pet food scientifically proven to deliver a difference pets will feel, and pet parents will see. We are a team united by a shared passion for pets and the people who love them. As a community...Full timeWork at officeRemote workRelocationMonday to Thursday- SUN PHARMA is seeking an Associate Compliance to support assessments of Global procedures and site procedures to ensure cGMP and QMS compliance. The role also compiles monthly quality metrics and analyzes trends to drive CAPAs and corrective actions. Responsibilities include...
- EMD Serono, Inc. in Massachusetts seeks an Associate Director, Global Regulatory Affairs Lead to own regional regulatory strategy and execution. This onsite role offers hybrid flexibility with a Tuesday-Thursday onsite presence. The ideal candidate will lead a regional...
$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- ...industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive...
$215k - $225k
...aviation safety. The CAO ensures the safety, efficiency, and regulatory compliance of aviation operations and respects and preserves... ...aviation specific training for clinicians and communication specialists. Conduct performance evaluations of direct reports and support...Full timeContract workImmediate startWeekday work$80k - $140k
Business Analyst - Data Integration and ETL, AVPSummary The Business Analyst, AVP will support data integration and ETL capabilities, with a focus on understanding business needs, documenting requirements, and helping improve existing and new ETL designs. This role will...Full timeTemporary workFlexible hours- Stark Pharma Solutions Inc. in Massachusetts seeks a Technical Compliance Associate to support GMP manufacturing and Quality activities in a regulated environment, focusing on investigations, deviations, NCRs, CAPAs, change controls, and batch documentation. You will partner...
$165k
Project Manager IIAs Project Manager II, you will be responsible for the overall success of assigned projects from preconstruction through closeout. Working in close partnership with field leadership, you will oversee project finances, procurement strategies, scheduling...Contract workFor subcontractorLocal area- Data AnalystLexington, MA, United StatesAbout the JobAs a Data Analyst in the Finance Data Analytics department, you will be responsible for maintaining, improving, and building new reporting capabilities for cross-functional areas of the business. By developing a deep...Work experience placementWork at office
$80k - $90k
...Manufacturing Compliance Specialist IAt Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe... ...manufacturing documentation, respond to auditor requests, and support regulatory inspections as a manufacturing subject matter resource.Provide...For contractorsWork at officeImmediate startMonday to FridayWeekend work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Specialist. Be the first to apply!
- regulatory engineer Bedford, MA
- regulatory cmc Bedford, MA
- regulatory Bedford, MA
- regulatory law Bedford, MA
- regulatory contract Bedford, MA
- vendor compliance Bedford, MA
- regulatory compliance Bedford, MA
- vice president regulatory affairs Bedford, MA
- regulatory affairs assistant Bedford, MA
- corporate compliance Bedford, MA




