Senior Regulatory Affairs Lead for Medical Devices
Boston Scientific - Minnetonka
Boston Scientific in Minnesota and Massachusetts offers a hybrid work model for a Senior Regulatory Affairs Specialist. You will develop regulatory strategies, prepare global submissions, and partner with cross-functional teams to ensure lifecycle compliance of implantable medical devices. You will mentor team members, coordinate regulatory reviews, and drive continuous improvement of our regulatory processes across development and integration initiatives. #J-18808-Ljbffr Boston Scientific
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Senior Regulatory Affairs Lead for Medical Devices in Osseo, MN vacancy
- Johnson & Johnson MedTech in Plymouth, MN seeks a Sr Program Lead, Regulatory Affairs to lead global regulatory strategies for medical devices and ensure timely commercialization in compliance with FDA and worldwide regulations. The role requires a Bachelor's degree in...SeniorMedical deviceWorldwide
$109k - $174.8k
...recognize their merit. Job Function Regulatory Affairs Group Job Sub Function Regulatory Affairs... ...is currently seeking a Sr Program Lead, Regulatory Affairs to join our team located... ...issues. Develops 510K submissions for medical devices for commercialization in the USA....SeniorMedical deviceTemporary workLocal areaWorldwide- Boston Scientific in Minnesota is seeking a Regulatory Affairs professional to support the Urology Complaint Management Center in a fast-paced environment. You will analyze customer complaints to determine regulatory reportability and coordinate with internal teams, field...SeniorMedical deviceWork at office
- ...Clinical Risk Evaluation (CRE) Senior Scientist/Program... ...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and... ...product performance, medical affairs, Clinical R&D, Quality Engineering, regulatory affairs, product...SeniorMedical deviceWork experience placement
Abbott
Maple Grove, MN1 day ago - ...whatever your ambitions. Senior Legal CounselAbout the... ...managing legal and regulatory risk. You will also help... ...be opportunities to lead or participate in broader... ..., and Regulatory Affairs.Advise on FDA, FTC and... ...guidance affecting the medical device industry.Participate in...SeniorMedical deviceHourly payFixed term contractWork at officeLocal areaShift work3 days per week
- ...Senior Regulatory Affairs Specialist Work mode: Hybrid Onsite Location(s): Marlborough... ...business provides proven, leading solutions to treat several... ...relationships with device reviewers through oral and... ...related discipline within the medical device industry, including...SeniorMedical deviceWork at officeLocal area3 days per week
Boston Scientific
Maple Grove, MN4 days ago - TALENT Software Services is seeking a Senior Chemist to join the PVH R&D team. This role focuses on developing, characterizing, and validating medical device products for venous disease, with emphasis on chemistry support for released and emerging products. You will collaborate...SeniorMedical device
- ...Implantable Systems (AIS) R&D organization is seeking a Senior AI Solutions Lead to join our AI Transformation core team and translate engineering... ...management.Experience in health care, life sciences, medical devices or another highly regulated industry.Experience...SeniorMedical deviceHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week
- ...Job Role: Senior Design Assurance Engineer - Medical Device (Onsite - Arbor Lakes, MN) Contract Overview: From development to commercialization,... ...partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology....SeniorMedical deviceFull timeContract work
Pharmavise
Maple Grove, MNmore than 2 months ago - Cypress HCM is partnering with a medical device manufacturer in the Twin Cities to hire a Senior Manager of Regulatory Affairs and Design Assurance. You will lead regulatory and design assurance teams, shape the roadmap and operating strategy, and ensure regulatory, quality...SeniorMedical device
- ProPlate, a leader in medical device metallization, seeks a Chemistry Laboratory Manager to steer the chemistry lab, ensure regulatory compliance, and drive improvement across plating processes. You will lead a team, oversee testing and maintenance, and partner with Operations...Medical device
- ...job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory... ...related field.Minimum Experience: 7+ years of US and International medical device regulatory submission/approval experience, to include FDA,...SeniorMedical deviceFull timeImmediate start
- ...Saluda Medical is a commercial‑stage medical device company focused on developing treatments for chronic neurological... ...Reporting to the Sr. Director, Regulatory Affairs, the Senior Regulatory Affairs Specialist... ...the right thing Pioneering – Lead Boldly, Change Lives, Disrupt...SeniorMedical device
Saluda Medical
Minneapolis, MN1 day ago - We’re partnered with a mid-size Class II Medical Device business looking for a Senior Regulatory Affairs Manager. This is a fantastic opportunity to join a busy,... ...candidates with right to work only What You’ll Be Doing Leading the business’ US Regulatory Affairs operations,...SeniorMedical devicePermanent employmentFull time
$94k - $150k
Job TitleSenior Regulatory Affairs SpecialistJob DescriptionSenior Regulatory... ...Specialist, UltrasoundThe Senior Regulatory Affairs Specialist... ...of Conformity, and Medical Device Licenses—for various global... ...changes to existing products.Lead global regulatory intelligence...SeniorMedical deviceFull timeWork at officeImmediate startWork visaRelocation package3 days per week- A medical device manufacturing client is looking to hire a Senior Manager of Regulatory Affairs and Design Assurance in the Twin Cities. This person will lead regulatory and design assurance teams in support of enterprise objectives, establish the organizational roadmap...SeniorMedical deviceContract work
- ...513809Reference25-04468 Job Description: The Senior Regulatory Affairs Manager will play a crucial role in leading and managing the regulatory submissions, including... ...successful approval and launch of innovative medical devices. Responsibilities: Prepare, review, and...SeniorMedical device
- Job-ID32834640Reference26-01421Summary:We are urgently seeking a Senior Quality Engineer with strong hands-on experience in FDA-regulated medical device manufacturing.Roles & Responsibilities:10+ years of Quality Engineering experience in medical device manufacturing.Strong...SeniorMedical deviceContract work
- Boston Scientific is seeking a Senior Design Quality Engineer to support high-visibility quality initiatives and sustainment activities... ...and risk management are robust and compliant. The candidate will lead quality processes, mentor staff, and drive improvements in...SeniorMedical device
$89.2k
...hire an enthusiastic individual for a Senior Regulatory Affairs Specialist position (hybrid work mode)... ...our rapidly growing active implantable device portfolio. This role will be... ...years Regulatory Affairsexperience in the medical industry Prior experience with 510(k)...SeniorMedical deviceHourly payWork at officeLocal areaRelocationShift work3 days per weekBoston Scientific
Arden Hills, MN5 days ago- ...markets.Under minimal supervision, the Senior Regulatory Affairs Specialist will plan, manage and... ..., 510(k) submissions, investigational device exemptions (IDEs), CE marking submissions... ...affairs or related disciplines within the medical device industry, such as research and...SeniorMedical deviceHourly payWork experience placementWork at officeLocal areaRelocationRelocation packageShift work3 days per week
- Boston Scientific is hiring a Senior Design Quality Engineer for Bolt Integration at the Arbor Lakes Campus in Maple Grove, MN. The role... ...requires collaboration across R&D, manufacturing, supplier and regulatory functions to protect design intent and ensure safety and...SeniorMedical deviceRelocation package3 days per week
$171k - $195k
...Senior Medical Science Liaison At Vericel Corporation,... ...of Vericel's Medical Affairs strategy. Working cross... ..., Marketing, Regulatory Affairs, and Research... ...pharmaceutical, medical device, regenerative medicine... ...Science: Work with a leading regenerative medicine...SeniorMedical deviceFor contractorsRemote work$160k - $180k
Title Senior Manager of Quality and Regulatory Location Plymouth, MN Job Type Permanent Compensation... ...80,000 + Bonus Industry Medical Device and Healthcare... ...execution of clinical affairs processes, as well as product... ...assurance compliance. Leading efforts in support of...SeniorMedical devicePermanent employmentContract workWorldwideFlexible hours- ...Our client, a growing medical device company, is seeking a Supplier Quality Engineer to support... ...actions, and ensure suppliers meet regulatory and quality system requirements. The ideal... ...Supplier Quality Management Lead supplier corrective action requests (SCAR...SeniorMedical device
Custom Search
Maple Grove, MN5 days ago $100k - $130k
Cypress HCM is looking for a Senior Design Assurance Engineer in Maple Grove, Minnesota. This role involves ensuring quality input and deliverables for new product development in medical devices. Candidates should have over 5 years of experience in medical device development...SeniorMedical device$80k - $120k
...individual in this role assists with medical writing and regulatory documentation, including preparation... ...analyze domestic and international medical device regulations to ensure submission... ...detail and accuracy. Pay Rate: $80-120k Seniority level Mid-Senior level Employment...SeniorMedical deviceFull timeWork at officeCypress HCM
Minneapolis, MN1 day ago- ...passion for cutting‑edge medical technologies, join our... ...day in the life: The Senior Compliance Specialist... ...and patient safety by leading the end‑to‑end... ...and in alignment with regulatory and internal requirements... ...background in medical devices, healthcare or a related...SeniorMedical deviceWork at officeLocal areaFlexible hours
- ...join our team! ABOUT THE ROLE Senior Operations Manager We are... ...ensuring stability and compliance. Lead day-to-day manufacturing and... ..., with at least 5 years in medical device leadership. Preferred Experience... ...decision-maker with deep regulatory knowledge. Why Join Us Build...SeniorMedical device
ENvue Med
Minneapolis, MN3 days ago - ...Corporation is seeking a seasoned Project/Program Manager to lead complex development projects within a regulated medical device environment. You will coordinate cross-functional teams across engineering, quality, regulatory, and manufacturing to ensure timely delivery and...SeniorMedical device
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Regulatory Affairs Lead for Medical Devices. Be the first to apply!
Related searches
- senior manager tax Osseo, MN
- senior brand designer Osseo, MN
- senior manager accenture Osseo, MN
- senior information technology project manager Osseo, MN
- senior implementation engineer Osseo, MN
- senior Osseo, MN
- senior living Osseo, MN
- senior manager legal Osseo, MN
- sr technical product manager Osseo, MN
- senior storage engineer Osseo, MN