Principal Regulatory Affairs - Ad & Promo, Med Devices
Boston Scientific Gruppe
A global medical technology leader is seeking a Principal Regulatory Affairs Specialist in Maple Grove, MN. In this role, you will review and ensure compliance of advertising and promotional materials for medical devices. The position requires a minimum of 5 years in regulatory affairs and a Bachelor's degree in a relevant field. You will work collaboratively, assessing product claims and providing regulatory feedback. This role follows a hybrid work model, requiring onsite presence three days a week, and offers a competitive salary range. #J-18808-Ljbffr
Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Principal Regulatory Affairs - Ad & Promo, Med Devices in Maple Grove, MN vacancy
$102.1k
...Principal Regulatory Affairs Specialist - Advertising & Promotion (Ad Promo) Onsite Location(s): Maple Grove, MN, US, 55311 Additional Location(s): US-MN-Maple Grove Diversity... ...support and training materials for medical devices used in interventional cardiology. The role...PrincipalHourly payWork at officeLocal areaShift work3 days per weekBoston Scientific Gruppe
Maple Grove, MN5 days ago$102.1k
...Additional Location(s): US-MN-Maple Grove About the role: This Regulatory Affairs Principal role supports the review and approval of advertising, promotional, sales support and training materials for medical devices used in interventional cardiology. The role applies a risk...PrincipalWork at officeLocal area3 days per weekBoston Scientific
Maple Grove, MN1 day ago- A leading medical device company is seeking a Principal R&D Engineer to drive product development from concept to commercialization. In this role, you... ...projects while ensuring compliance with quality and regulatory standards. The ideal candidate has over 7 years of experience...Principal
$102.1k - $194k
...at least three days per week. Responsibilities Represent the Regulatory Affairs function on cross‑functional teams for new product... ...regulatory strategies and prepare submissions for Class II medical devices. Create innovative regulatory pathways that support new technologies...PrincipalWork at officeLocal areaOverseas3 days per weekBoston Scientific Gruppe
Maple Grove, MN11 hours ago- ...reflecting the culture our employees experience every day.The Principal Regulatory Affairs Specialist is responsible for planning, managing and... ...regulatory strategies and prepare submissions for Class II medical devices.Create innovative regulatory pathways that support new...PrincipalHourly payWork at officeLocal areaWorldwideShift work3 days per week
Boston Scientific
Maple Grove, MN1 day ago $100k - $120k
...Engineer II to lead supplier management activities and ensure regulatory compliance. You will collaborate across teams, drive quality improvements... ...processes to enhance patient care through innovative medical devices. The ideal candidate has a bachelor's degree in engineering...- Boston Scientific in Minnesota seeks a Regulatory Affairs Principal to review and approve advertising, promotional, sales support and training materials for interventional cardiology devices. The role applies a risk-based regulatory mindset to ensure accuracy, balance,...Work at office3 days per week
- ...Boston Scientific Gruppe is seeking a Regulatory Affairs professional to join their Interventional Oncology and Embolization team in Maple... ...regulatory strategies and managing submissions for Class II medical devices, ensuring compliance with both US and EU regulations. The...
Boston Scientific Gruppe
Maple Grove, MN11 hours ago - B Capital in Maple Grove, Minnesota, is seeking a Principal Regulatory Affairs Specialist to join their Interventional Oncology and Embolization team. This role is responsible for planning and managing regulatory submissions to FDA and EU, supporting new product development...Work at office3 days per week
- Teleflex is seeking a mid-level Regulatory Affairs professional to manage regulatory processes throughout the product lifecycle. This role... ...ideal candidate will have 2-5 years of experience in medical devices, strong analytical skills, and proficiency in Microsoft Office...Work at office
- Job Description Job Description ~ Lead electrical engineering efforts from concept through production, owning both schematic design and PCB layout in a fully integrated development environment. ~ Serve as the technical lead for electrical engineering-focused...PrincipalLocal area
Medix
Maple Grove, MNa month ago - ...key member of the Manufacturing team, the Principal Manufacturing Engineer will assist in... ...and ensuring manufacturing processes meet regulatory and performance requirements. Provide... ...+ with Master's), preferably in medical device industry; Bachelor's in Mechanical,...PrincipalWork at officeFlexible hours
Laborie Medical Technologies Corp
Plymouth, MN5 days ago - ...Neuromodulation, CAHF and Vascular products. You will evaluate clinical evidence from studies, literature, and surveillance, and collaborate with regulatory, quality, and R&D teams to ensure compliant submissions and risk management. #J-18808-Ljbffr Abbott Laboratories
$130k - $160k
...Nextern is seeking a talented Principal Electrical Engineer to join... ...systems for medical devices. You will work collaboratively... ...excellence and compliance with regulatory standards. DUTIES AND RESPONSIBILITIES... ..., Long Term Disability, and AD&D Life Insurance...PrincipalTemporary workNextern
Osseo, MN25 days ago- Project Specialist II — Medical Device (Hybrid — Maple Grove, MN) Possible Temp-to-Hire Maple... ...technical expertise in Quality, Regulatory Compliance and Manufacturing Science and... ...Interventional Spine commercial team. Manage ad hoc tasks and requests to support the team...Temporary work3 days per week
$102.1k
...reflecting the culture our employees experience every day. This Regulatory Affairs Principal role supports the review and approval of advertising, promotional, sales support and training materials for medical devices used in interventional cardiology. The role applies a risk...PrincipalHourly payWork at officeLocal areaShift work3 days per week- ...documenting processes, managing nonconformances, and supporting compliance with regulatory standards. Candidates should have a Bachelor's Degree in life sciences and significant experience in medical device development. Benefits include health care plans, retirement matching,...
- Boston Scientific Gruppe is seeking a Principal Sales Training Specialist to design, deliver, and evaluate comprehensive sales training... ...candidate will have at least 7 years of experience in medical device sales and a proven track record in training facilitation. This...PrincipalRemote job
- Boston Scientific is hiring a Principal Regulatory Affairs Specialist in Maple Grove, MN, to lead regulatory strategy for a broad ablation portfolio. The role involves coordinating IDEs, 510(k)s, and EU MDR submissions, collaborating across R&D, Quality, Operations and...
- ...update labeling and product information for medical devices, manage data, and drive the labeling change process to support patient safety and regulatory compliance. The candidate will collaborate with Regulatory Affairs, Quality, R&D, Packaging, Clinical and Marketing,...Work at office
- A leading medical device company in Maple Grove, MN is seeking a Marketing Communications Specialist II to manage Marketing Operations and develop subject matter expertise in industry compliance. The role demands at least 2 years of experience in the medical device sector...Contract work
$85k - $95k
A leading medical device organization in Minnetonka is seeking a Senior Accountant to support financial operations and reporting. This role collaborates with the Financial Controller on compliance and strategic analysis. The ideal candidate will hold a Bachelor’s degree...$113.03k - $165.77k
...job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory approvals... ...Minimum Experience: 7+ years of US and International medical device regulatory submission/approval experience, to include FDA,...Immediate startInteger Holdings Corporation
Plymouth, MN2 days ago$150.5k - $286k
A leading medical device company is seeking a Program Management Director in Maple Grove to drive new product introduction strategies and oversee the project portfolio. This role requires extensive experience in Manufacturing and Project Management, as well as strong leadership...$55k - $75k
...looking for a detail-oriented Quality Inspector to ensure precision-manufactured components meet quality standards in the medical device sector. In this role, you will carry out both in-process and final inspections using calibrated equipment and maintain documentation...- Seeking a Principal R&D Engineer to lead medical device product development from concept through commercialization. This role drives cross‑functional teams... ...of new devices in alignment with quality system and regulatory requirements Translate user needs into validated...Principal
- ...qualifications include a Bachelor’s degree in Engineering and a minimum of 5 years' experience in design assurance within the medical device industry. Competitive salary range is offered, along with benefits including medical insurance and a 401(k). #J-18808-Ljbffr...
- ...Principal Research and Development Engineer page is loaded## Principal... ...business challenges and/or regulatory issues, reviews and recommends... ...introduction of value-adding, technical solutions and leads... ...Qualifications:* 12 years of Medical Device design & development...Principal
Freudenberg Group
Minnetonka, MN1 day ago - ...A leading medical device company is seeking a Project Specialist II for their Interventional Spine Team in Maple Grove, MN. This role involves managing vendor processes, leading market research, and generating data analytics from Salesforce and Tableau. The ideal candidate...3 days per week
Pharmavise Corporation
Maple Grove, MN5 days ago - ...Senior Regulatory Affairs Specialist At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in... ...domestic and international strategies for Class II and III medical devices Represent RA on cross functional projects which may...Permanent employment
Intracept by Boston Scientific
Maple Grove, MN3 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Principal Regulatory Affairs - Ad & Promo, Med Devices. Be the first to apply!
Related searches
- principal Maple Grove, MN
- regulatory law Maple Grove, MN
- regulatory contract Maple Grove, MN
- regulatory engineer Maple Grove, MN
- regulatory Maple Grove, MN
- food regulatory Maple Grove, MN
- compliance technician Maple Grove, MN
- compliance team leader Maple Grove, MN
- legal compliance Maple Grove, MN
- customs compliance Maple Grove, MN