Medical Device Project Manager - Lean & Regulatory
$85k - $115kFreudenberg Medical
A leading medical device manufacturer is looking for a skilled Project Manager in Minnetonka. You will lead projects focused on manufacturing cost models, track performance metrics, and ensure compliance with ISO standards. The ideal candidate has a degree in a relevant field and significant experience in the medical device industry, with proven leadership in manufacturing environments. The position offers a salary range of $85,000 to $115,000 annually based on qualifications. #J-18808-Ljbffr Freudenberg Medical
$130k - $150k
Principal Regulatory Affairs Project Manager - Medical Devices Global medical device manufacturer | Hybrid (3 days onsite) | Regulatory Affairs The role Our client, a long-established global leader in medical devices and combination products, is hiring a senior regulatory...Medical device$85k - $115k
...moments. Freudenberg Medical is a trusted Contract... ...production for medical device and pharmaceutical companies... ...LLC. * Position Project Manager Responsibilities... ...continuous-improvement and Lean/Six Sigma activities... ...efficiency, innovation, and regulatory excellence across the...Medical deviceContract workWork at office$160k - $180k
Senior Manager of Quality and Regulatory Plymouth, MN55441 Posted: 07/09/2026 Employment Type:... ...0,000 - $180,000 + Bonus Industry: Medical Device and Healthcare Technology --- About... ...improvement approaches. Participating in project teams to provide regulatory and...Medical devicePermanent employmentContract workLocal areaWorldwideFlexible hours$135k - $145k
...everything possible.The Technical Project Manager, Global Operations for... ...with Quality, Regulatory, and Operations stakeholders... ...technology transfer projects in the Medical Device or Diagnostics regulatory environment... ...13485 and global standards.Lean Six Sigma: Proficiency in...Medical deviceFull time- ...Global Market Intelligence, Cardiac Rhythm Management The not to exceed bill rate set by... .... Ability to effectively prioritize projects that align with corporate priorities. Excellent... ..., organization and communication skills. Medical device experience. Ova TechnologiesMedical deviceHourly pay
- ...Owners to prioritize and manage backlogs aligned with... ...Management, QA, Regulatory, and Clinical Affairs... ...healthcare software, medical devices, or other regulated industries... ...Agilist, PMI-ACP, or Lean Six Sigma are a plus.... ...00 - 117,900.00Department:Project/Program ManagementMedical deviceLive inLocal area
$171k - $273k
Job TitleDirector of Regulatory Affairs - RespirTech (Plymouth, MN)... ...strategies and quality team/quality management system (QMS)... ...cross-functional programs and projects.Manage/oversee execution of... ...Operations within the FDA regulated Medical Device industry, including 3+ years...Medical deviceFull timeWork at officeImmediate startWork visaRelocation package3 days per week$65k - $85k
...Job Description Job Title: Project Coordinator – Equipment Systems & Vendor Management Job Description The Project... ...with internal procedures and regulatory expectations. The Project Coordinator... ...pharmaceutical, biotech, or medical device environment with a high school...Medical devicePermanent employmentWork at office$116k - $125k
Technical Project Manager, Global Operations - Beckman Coulter Diagnostics... ...Collaborate with Quality, Regulatory, and Operations... ...technology transfer projects in the Medical Device or Diagnostics regulatory environment... ...standards. Proficiency in lean six sigma tools and problem...Medical device- ...Project Manager From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues... ...providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science...Medical deviceContract work
- ...company is seeking a Senior Operations Manager in Plymouth, Minnesota. The role involves... ...daily manufacturing operations, driving lean initiatives, and managing the supply chain... ...experience, emphasizing leadership in medical devices. If you're a strategic thinker and team...Medical device
$71.5k
...facility modification projects within manufacturing and... ...that support medical device production and research... ...ensuring compliance with regulatory requirements and minimizing... ...Develop and manage end-to-end project plans... ...Experience utilizing lean manufacturing tools...Medical deviceHourly payFull timeFor contractorsWork at officeShift work$181k - $288k
Job TitleDirector, Quality & Regulatory- Mergers & Acquisitions (M&A)Job DescriptionThe Director... ...through post-close. The Director also manages quality and regulatory risks,... ...years’ experience in FDA regulated global medical device environments (Class III products/devices...Medical deviceFull timeWork at officeImmediate startWork visaRelocation package3 days per week- 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, energetic... ...functionally with R&D and Quality on strategic projects including New Product Development and...Medical devicePermanent employmentFull time
- ...Abbott Laboratories is seeking a Program Manager R&D to lead cross-functional teams in Plymouth, MN. The role focuses on new product... ...The ideal candidate will have over 8 years of experience in medical device development, a relevant technical degree, and strong...Medical device
$162k - $258k
...Philips’ Image Guided Therapy Devices quality organization, focused... ...compliance and effective Management Review processes/reporting.Your... ...compliant with the applicable regulatory requirements, industry standards... ...in global, FDA regulated medical device environments, including...Medical deviceFull timeWork at officeImmediate startWork visaRelocation package3 days per week- FloodGate Medical is seeking a senior Quality & Regulatory Director to lead the quality systems, regulatory compliance, and design assurance for the Aquadex... ...Clinical teams to ensure safe, high-quality medical devices while shaping the product portfolio’s development and...Medical device
- ...Medical Device Assembly Technician The Medical Device Assembly Technician performs assembly, inspection, testing, and packaging of medical devices while following GMP and FDA regulations. Key Responsibilities Assemble medical devices using hand tools. Inspect...Medical device
$170k - $270k
...Title Director, Quality Management Systems & Compliance Job... ...to executive leadership on regulatory changes, compliance risks, and... ...identify, prioritize, and lead projects aimed at improving quality... ...experience in FDA regulated medical device environments, with extensive...Medical deviceFull timeWork at officeImmediate startWork visaRelocation package3 days per week- FloodGate Medical is seeking a Quality & Regulatory Director to lead the Quality Systems, Regulatory, Design Assurance, supplier quality, and contract manufacturing... ...indications. The role requires 8+ years in medical device quality, ISO 13485/14971 familiarity, and a startup-...Medical deviceContract work
$140k - $185k
...POSITION SUMMARY: The Senior Manager, Manufacturing Operations... ...environment in the medical device or pharmaceutical industry which... ...quality systems, ISO standards, regulatory expectations, audit... ...mindset with experience applying Lean Manufacturing, Six Sigma, 5S...Medical deviceWork at officeShift work- A healthcare company in Eden Prairie is searching for a Sr Project Manager. This position is remote and involves managing critical projects... ...collaboration and communication skills are essential, along with a history in medical device manufacturing. #J-18808-Ljbffr SolventumMedical deviceRemote job
- ...-04468 Job Description: The Senior Regulatory Affairs Manager will play a crucial role in leading... ...successful approval and launch of innovative medical devices. Responsibilities: Prepare, review... ...on regulatory strategies and project timelines. Represent the company in...Medical device
$85k - $125k
...Job Description Job Description A medical device client in New Hope, Minnesota is seeking a Research & Development (R&D) Project Manager to lead complex, customer-facing development... ...understanding of design control and regulatory requirements (FDA, ISO 13485)....Medical device- ...post-market—focusing on requirements management, risk analysis, system integration, and... ...verification/validation within a regulated medical device environment.Roles & Responsibilities:... ...from cross-functional inputs (regulatory, quality, manufacturing, service, etc....Medical device
$19.25 per hour
...Medical Device Assembler HireGenics is immediately hiring for Medical Device Assemblers. As a Medical Device Assembler you will: Responsible to produce high-quality medical devices. Perform a combination of assembly, repair, and test operations on pacemakers...Medical deviceFull timeContract workTemporary workImmediate startRemote workAfternoon shift$60k - $80k
...Job Description Job Description A medical device client in Maple Grove, Minnesota is looking to hire a Logistics Project Manager to keep their clinical field operations running smoothly. This person will be in charge of coordinating schedules, travel, shipment of...Medical device- ...development Experience creating and managing backlogs, tracking execution... ...Mobile Software Development Project Planning Software Project... ...control of interconnected medical devices.As a Senior Software... ...lifecycle processes Support regulatory deliverables in collaboration...Medical device
$200k - $220k
...technical and non-technical projects, and building the... ...and Portfolio Management Office infrastructure... ...experience in diagnostic/medical device regulated environment... ...Device or Diagnostics regulatory environmentExcellent... ...previous experience in:Lean /Six Sigma experience...Medical deviceHourly payFull timeRemote workWork from homeFlexible hours- ...of Stereotaxis’ systems have received regulatory clearance in the United States, European... ...please visit Position Summary: The Project Manager will be responsible for overseeing and... ...FDA, ISO 13485, and other relevant medical device industry regulations and standards. Identify...Medical deviceFull timeWork at office
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