VP of Regulated Medical Device Engineering
Hims & Hers
Hims & Hers is looking for a VP, Regulated Device Engineering to lead the medical device business. This role involves overseeing R&D, ensuring compliance with FDA and global regulations, and driving product innovation. The ideal candidate will have over 15 years of experience in the medical device industry, a Bachelor's degree in Mechanical Engineering, and a proven track record in product development and regulatory processes. Hims & Hers offers a competitive salary, unlimited PTO, and comprehensive health benefits. #J-18808-Ljbffr Hims & Hers
$130k - $170k
Freudenberg Group is hiring a Principal Product Development Engineer in Minnetonka, Minnesota. This role demands 12 years of experience in medical device design and development, along with a Bachelor's degree in Mechanical or Biomedical Engineering. The position offers...Suggested- About the Role: The VP, Regulated Device Engineering is responsible for the overall leadership, strategy, and execution of the company’s regulated medical device business organization. This role owns end‑to‑end product development, from concept through commercialization...SuggestedFull timeLocal area
$220k - $225k
Trelleborg Medical Solutions is seeking a VP Global Quality and Regulatory, based from... ...of life‑saving devices. Growth and advancement:... ...Represents the company with regulators, industry bodies and external... ...environments to deliver pioneering, engineered solutions for...SuggestedFixed term contract$39 - $42 per hour
...A leading medical device firm in Minnetonka is seeking a Production Supervisor to lead and develop team members while ensuring safety and... ...ideal candidate has 3-5 years of leadership experience in a regulated manufacturing environment and can effectively communicate and...SuggestedHourly pay- ...Summary The Medical Device Assembly Technician performs assembly, inspection, testing, and... ...medical devices while following GMP and FDA regulations. Key Responsibilities Assemble medical... ...Follow cleanroom procedures. Support engineering builds when required. Education High...Suggested
- ...Company Growing cardiovascular medical device company leading commercial... ...of the QMS, quality engineering, clinical quality, supplier... ...implantable product space. The VP of Quality Assurance will also... ...a deep understanding of FDA regulations, ISO standards, design controls...
- ...Company Growing cardiovascular medical device company with commercial... ...of the QMS, quality engineering, clinical quality, supplier... ...implantable product space. The VP of Quality Assurance will be... ...a deep understanding of FDA regulations, ISO 13485, ISO 14971, design...
- ...The Position The VP Government & Community Health Affairs is responsible for the government relations activities on behalf of Johns... ...Commands respect in high-stakes environments with policymakers, regulators, and board members. # Able to navigates complex, politically...Full timeLocal area
- ...regions, including the East Baltimore medical campus, Johns Hopkins Bayview Medical Center... ...and foster deep respect for design and engineering operations. # Leads Capital Project... ...Knowledge of Federal, State, and local regulations and codes. # Highly proficient in...Full timeWork experience placementLocal areaShift work
- ...The Position The VP of HR at Johns Hopkins Bayview Medical Center (JHBMC) will be the Human Resource Leader for the JHBMC and its various entities... ...ensures compliance with related federal and local laws and regulations. # Contributes to long and short-term planning and...Full timeTemporary workLocal area
$50 - $78 per hour
Contract Manufacturing Engineer ~Location: On-site, Minneapolis Area, MN ~Pay Rate:... ...product introduction activities within a regulated manufacturing environment. This role... ...~4+ years of engineering experience in medical device, life sciences, or other regulated manufacturing...Hourly payContract workFreelance$200.4k - $343.5k
...Engineering Leadership Role Optum Tech is a global leader in health care innovation. Our teams develop cutting-edge solutions that... ...explainability, model risk management, and compliance with healthcare regulations Healthcare Compliance, Security & Responsible AI...Minimum wageFull timeWork experience placementLocal area$60k - $70k
A dynamic medical device company in Minnetonka is looking for a Senior Lab Technician to oversee biological safety testing and manage quality... ...experience in medical devices, familiarity with ISO and FDA regulations, and strong communication skills. Responsibilities include...$50.8k - $76.13k
Medica is looking for an Executive Assistant in Hopkins, Minnesota, to provide advanced administrative support to a Vice President and help coordinate departmental activities. Candidates should possess a high school diploma and at least 4 years of administrative experience...Work at office$81k - $101k
...multiple priorities, effectively delegate, and set deadlines. Ability to identify and facilitate change in a deadline driven, highly regulated environment. Excellent problem‑solving skills and attention to detail. Ability to work well under pressure and be able to meet...16 hoursFull timeTemporary workPart timeWork experience placementWork at officeImmediate startMonday to Friday$50.8k - $76.13k
...travel arrangements. Candidates should have a high school diploma, 4+ years of relevant experience, and proficiency in Microsoft Office Suite. The typical salary range is $50,800 - $76,125, with benefits including medical, dental, and retirement plans. #J-18808-Ljbffr MedicaWork at office$50.8k - $76.13k
A nonprofit health organization is seeking an Executive Assistant in Minnetonka, MN. This role offers advanced administrative support to a Vice President, coordinating calendars, preparing reports, and serving as a key contact for the department. Candidates should have ...Work at office3 days per week- Laborie Medical Technologies Corp is looking for a Clinical Program Manager in Minnetonka, MN. The CPM will manage clinical research... ...collaboration on evidence strategy, and ensuring compliance with regulations. Ideal candidates should have a Bachelor's degree in a...
- Freudenberg Medical LLC seeks an experienced Program Manager to lead complex medical device development and manufacturing projects. You will drive cross‑functional teams... ...programs under applicable medical device regulations. #J-18808-Ljbffr Dormont Manufacturing Co
- ...role collaborates with the COO and executive leaders to shape talent strategies and influence organizational design within a highly regulated environment. The ideal candidate will have 10-15 years of progressive HR experience, including significant executive support in...
- ...Job Title - Automation Engineer Duration - 6 Months Contract with high chances of extension MoI - Video Location - Hopkins, MN - 3 days per week.(Hybrid ) Job Description : Languages: Java, Groovy, JavaScript Automation Tools & Framework...Contract work3 days per week
- ...to support production of minimally invasive heart devices at our Minnetonka site. This role plays a critical part... ...production lines. You will work primarily in a regulated clean room environment supporting medical device manufacturing for Abbott , with additional...
$80k
...ensuring compliance with all federal and state regulations. You will be responsible for financial... ...skills and familiarity with electronic devices ~ Flexibility to work varied schedules... ...~ Relocation assistance offered. ~ Medical, Dental, & Vision Insurance ~401(k)...Full timePart timeReliefRelocation package$200k
...Eden Prairie, MN, US, 55344 Business Unit: Advanced Medical Components Posting Date: May 30, 2026 This... ...building a scalable, resilient global operations engine that enables AMC and AMETEK to win in highly regulated, high value medical markets. The Divisional Vice President...Local area- Laborie Medical Technologies Corp in Minnetonka, MN is seeking a Medical Writer II to develop clinical and regulatory documents... ...years of relevant writing experience and knowledge of medical device regulations. Laborie offers various benefits including health insurance...
$24 per hour
...education will be taken into account). Professional Experience: At least 1 year of hands‑on experience inside a regulated pharmaceutical or medical device production setting. Environment Comfort: Able to work productively within a controlled cleanroom setting, which includes...Shift workDay shiftAfternoon shift$39 - $42 per hour
...that established policies, work rules, regulations and procedures are distributed to and... ...regulated manufacturing environment, i.e. medical devices or other industries governed by FDA,... ...partnering with other functions (i.e. Engineering, Quality, Logistics) in a...Hourly payWork at office- ...effectively with stakeholders. Responsibilities: Kitting of medical device production orders in a clean room environment by accurately... ...documents at a middle school level. Strict adherence to regulated procedures. Qualification And Education: ~ High school...For contractors
$85k - $104k
...study protocol, GCP/ICH, and applicable regulations. Conduct initial and ongoing training... ...with the preparation of clinical study devices and verify accountability of investigational... .... Ensure adverse events, concomitant medications, and inter‑current illnesses are...Work at officeLocal area- ...Construction Power Lines Civil Engineering Utilities Electricians Contractors... ...and warehouse, safety, and quality. The VP of Operations will be a key driver of operational... ...standards, quality control, and OSHA regulations is essential, and experience in utility,...For contractors
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