Medical Device Labeling & Regulatory Projects Lead
Teleflex
Teleflex is seeking a Labeling Specialist to join our Maple Grove, Minnesota office. This role will create 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, deliver training, and mentor labeling coordinators. #J-18808-Ljbffr Teleflex
$71.5k - $135.8k
Boston Scientific is seeking a Project Manager in Maple Grove, Minnesota to lead facility modification projects supporting medical device production. This on-site role will involve overseeing... ...while ensuring compliance with regulatory standards. The ideal candidate holds a...RegulatoryMedical device$71.5k - $135.8k
Boston Scientific Gruppe is seeking a Project Manager to lead facility modification projects at their Maple Grove, Minnesota location. This... ...planning, design, and execution while ensuring compliance with regulatory requirements and budget constraints. Candidates should be...RegulatoryMedical device- Actalent in Maple Grove, MN seeks a Senior Project Manager to lead medical device product development from concept through commercialization. You will... ..., and risks to align with customer requirements and regulatory standards. The role demands hands‑on leadership, strong...RegulatoryMedical devicePermanent employment
$69.7k - $89.6k
...global provider of medical technologies,... ...Teleflex is seeking a Labeling Specialist to join... ...information for medical devices to optimize... ...labeling data, maintain project documentation, and... ...to ensure regulatory compliance to support... ...Responsibilities Leads development of medical...RegulatoryMedical deviceTemporary workFlexible hours$88k - $130k
...Summary This is a mid‑level Regulatory Affairs position responsible... ...lifecycle and coordinating projects effectively. The role supports... ...to commercially distributed medical devices Conduct appropriate research... ...Review and approve product labeling, advertising, and promotional...RegulatoryMedical deviceTemporary workWork at officeFlexible hours- ...for cutting-edge medical technologies, join... ...product development projects. Contribute to the... ...and reliability. Lead or participate in... .... Support product labeling updates and artwork... ...management, medical device development, and... ...and maintenance of regulatory requirements...RegulatoryMedical deviceHourly payFull timeWork at officeLocal areaMonday to FridayFlexible hours
- ...Senior Regulatory Affairs Specialist At Boston Scientific, we'll give... ...strategies for Class II and III medical devices Represent RA on cross functional projects which may include product development... ..., Clinical, Biocompatibility, Labeling, etc) ~ Demonstrated...RegulatoryMedical devicePermanent employment
$102.1k
...Grove About the role: This Regulatory Affairs Principal role supports... ...and training materials for medical devices used in interventional... ...questions related to evidence, labeling alignment and risk communication... ...Ability to manage multiple projects and meet deadlines in a fast...RegulatoryMedical deviceWork at officeLocal area3 days per week$88k - $130k
...Regulatory Affairs Specialist Date: Jun 26, 2026... ...a global provider of medical technologies, Teleflex... ...lifecycle and coordinating projects effectively. The role... ...commercially distributed medical devices • Conduct... ...Review and approve product labeling, advertising, and...RegulatoryMedical deviceTemporary workWork at officeFlexible hours- ...Core Responsibilities Support and lead Design History File (DHF) Remediation activities for sustaining medical device products. Perform gap assessments, evidence... ...Support audit/inspection readiness and regulatory compliance. Collaborate with R&D, Manufacturing...RegulatoryMedical device
- A leading engineering firm is seeking a Quality Engineer for a hybrid role in Maple Grove... ..., and ensuring compliance with regulatory standards. The ideal candidate will have... ...design quality assurance, particularly in medical device development. Strong communication and collaboration...RegulatoryMedical device
$102.1k
...Principal Regulatory Affairs Specialist - Advertising & Promotion... ...and training materials for medical devices used in interventional cardiology... ...related to evidence, labeling alignment and risk communication... ...Ability to manage multiple projects and meet deadlines in a fast...RegulatoryMedical deviceHourly payWork at officeLocal areaShift work3 days per week- ...Boston Scientific Gruppe is seeking a Regulatory Affairs professional to join their Interventional... ...and managing submissions for Class II medical devices, ensuring compliance with both US and... ...of relevant experience, with proven project management and technical writing skills...RegulatoryMedical device
- Medical Engineering Consultants (MEC) seeks a Mid-Level Quality Engineer on a contract basis to support design assurance for the TheraSphere... ...with cross-functional teams to ensure safety, quality, and regulatory compliance by reviewing design control deliverables and...RegulatoryMedical deviceContract work
- ...technologies. The company seeks professionals for Clinical & Regulatory Affairs roles to support clinical research and regulatory... ...development opportunities. Candidates with experience in Class III medical devices are especially encouraged to apply. #J-18808-Ljbffr Anteris...RegulatoryMedical device
- ...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,...RegulatoryMedical device
- ...Our client, a growing medical device company, is seeking a Supplier Quality... ..., and ensure suppliers meet regulatory and quality system... ...Quality Management Lead supplier corrective action requests... ...quality improvement projects. Support risk management...RegulatoryMedical device
$18.22 - $25.53 per hour
...quality standards to produce high-quality medical device components and products. Shift... ...Quality System, ISO, and medical device regulatory requirements. Communicate issues with... ..., band, or impulse sealers. Perform labeling, packaging, and final presentation of product...RegulatoryMedical deviceTemporary workWork at officeShift workDay shift- ...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... ...advertising and promotional materials for medical devices. The position requires a minimum of 5 years in regulatory...RegulatoryMedical device3 days per week
- ...to play a crucial role in ensuring manufacturing quality and regulatory compliance. This position involves collaboration with engineering... ...have a solid background in manufacturing quality within a medical device company. Anteris offers a dynamic work environment and...RegulatoryMedical device
- ...seeking a Technical Writer/Editor/Proofer for labeling and IFU documentation. You will author,... ...lifecycle, ensuring accuracy and regulatory compliance. Collaborate with engineering... ...The role emphasizes attention to detail, project management, and the ability to simplify...RegulatoryMedical device
- 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...RegulatoryMedical device
- Boston Scientific is seeking a Facilities Project Manager in Maple Grove, MN to lead planning, design and execution of facility modifications in manufacturing and laboratory environments for medical device production. You will ensure projects stay on schedule and within...Medical 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... ...to relevant personnel. Review device labeling and marketing materials to ensure compliance...RegulatoryMedical deviceFull timeWork at office$22 - $28 per hour
...inspections in a highly regulated medical device development and manufacturing... ..., first‑article inspections, label verifications, valve... ...Other tasks assigned by group lead or designee. Skills, Knowledge... ...with established safety and regulatory protocols. Must follow cGMP,...RegulatoryMedical deviceHourly payWork experience placementH1bLocal areaVisa sponsorshipWork visaMonday to FridayShift workDay shift$49 - $59 per hour
...Design History File (DHF) Ownership: Lead the creation, maintenance, and audit-readiness... ...all documentation meets internal and regulatory requirements. Risk Management: Own and... ...Development Engineering, preferably in medical device development. Strong knowledge of...RegulatoryMedical deviceContract work- Teleflex is seeking a mid-level Regulatory Affairs professional to manage regulatory processes throughout the product lifecycle. This... .... The ideal candidate will have 2-5 years of experience in medical devices, strong analytical skills, and proficiency in Microsoft...RegulatoryMedical deviceWork at office
$65.8k - $125k
...Product Analyst III based in Maple Grove, Minnesota. In this role, you will analyze customer feedback and manage regulatory submissions for medical devices. The position requires a Bachelor’s degree and at least 3 years of experience in medical device complaint handling...RegulatoryMedical device$100k - $120k
...MN, is seeking a Supplier Quality Engineer II to lead supplier management activities and ensure regulatory compliance. You will collaborate across teams, drive... ...to enhance patient care through innovative medical devices. The ideal candidate has a bachelor's degree in engineering...RegulatoryMedical device- ...Katalyst CRO is seeking a highly skilled Medical Device Labeling Engineer based in Minneapolis,... ...compliance with FDA and EU regulations, and leading labeling implementation activities.... ...emphasizes cross-functional collaboration and project management, making it essential to...Medical device
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