Senior Software Manager, Regulated Medical Devices
Real
Specialist Staffing Group is seeking a Senior Software Manager in the Twin Cities, MN area to lead software development and regulatory compliance for a novel therapeutic platform. This role oversees lifecycle documentation, verification/validation strategies, and cross-functional collaboration with quality and regulatory teams. You will be the initial software team leader, responsible for hiring, mentoring, and establishing scalable development processes to support early-stage systems through #J-18808-Ljbffr Real
- Senior Software ManagerTwin Cities, MNAbout the OpportunityAn innovative medical technology company is seeking a Senior Software Manager to lead software development and regulatory compliance efforts... ...62304 and related medical device regulations.Conduct software gap...SeniorMedical deviceFor contractors
- Integer Holdings is seeking an experienced Project/Program Manager to lead complex, regulated product development and engineering initiatives. You will drive end-to-end project execution, coordinate with cross-functional teams, and ensure milestones, budgets, and quality...SeniorMedical device
- Real Staffing is seeking a Senior Software Manager in the Twin Cities area to lead software development and regulatory compliance for a novel medical platform. You will drive software lifecycle activities, risk management, and verification/validation while transitioning...SeniorMedical device
- Teleflex is seeking a Sr. Facility Manager to lead and oversee facility operations across R&D, lab, and office environments at... ...coordinate with contractors, and partner with EH&S to uphold GMP standards within a regulated medical device context. #J-18808-Ljbffr TeleflexSeniorMedical deviceFor contractorsWork at office
$170k
Please see the below requirements for a Senior or Principal Electrical Engineer to join a growing class III medical device organization in the Northeast Twin Cities Metro.... ..., and targeted PCB/circuit updates within a regulated environment. This is an onsite role with flexiblity...SeniorMedical device$105k - $125k
Senior Manufacturing Engineerð Plymouth, MN ð¼ Direct Hire | ð $105,000-$125,000About... ...electromechanical capital equipment in a regulated environment.This is a highly execution-... ...in manufacturing engineering (medical device or regulated industry preferred)Experience...SeniorMedical device- Brio Group is partnering with a medical device leader to recruit a Senior Software Engineer for their cardiac care R&D team. You will develop software across... ..., manufacturing support, and post-market enhancements in a regulated environment. #J-18808-Ljbffr Brio GroupSeniorMedical device
$170k
Real is seeking a Senior/Principal Electrical Engineer to join a growing medical device organization in the Northeast Twin Cities Metro. The role focuses on verification... ..., and targeted PCB/circuit updates within a regulated environment. This onsite position offers a base...SeniorMedical device- ...leading recruiting firm is seeking a Senior Supplier Quality Engineer in... ...focuses on supplier qualification and management within the medical device industry. The ideal candidate will... ...a strong knowledge of ISO 13485 and FDA regulations. #J-18808-Ljbffr Staftonic LLCSeniorMedical deviceLong term contract
- Brio Group is seeking a Senior Quality Engineer to provide leadership and technical support in a regulated medical device environment. The role focuses on manufacturing quality, NPI, process validation, and continuous improvement, partnering with Operations, Engineering...SeniorMedical device
- Tactile Medical in Minneapolis, MN is seeking a Senior Firmware Engineer to design, develop, and maintain embedded software for regulated at-home medical devices. You will lead firmware features, perform integration and verification, and ensure release-ready quality. The...SeniorMedical device
- ...Senior Quality Engineer We are urgently seeking a Senior Quality Engineer with strong hands-on experience in FDA-regulated medical device manufacturing. Roles & Responsibilities: #10+ years... ..., FDA 21 CFR Part 820 & Risk Management. # Customer complaint investigations...SeniorMedical deviceContract work
- We are looking for an experienced Senior Legal Contracts Analyst to support commercial... ...cross-functional teams within a highly regulated environment. This Long-term Contract... ...regulatory research related to healthcare, medical device activities, and commercial operations...SeniorMedical deviceLong term contractContract work
- ...of manufacturing processes for highly regulated products.Drive technical problem-solving... ...environments strongly preferred, with medical device experience being a plus.Hands-on experience... ...making methodologies.Proven ability to manage technical projects, prioritize...SeniorMedical deviceLocal area
- .... We're partnering with an innovative medical device company that's redefining how complex... ...are performed. They're looking for a Senior Software Engineer to join their growing R&D team... ...solving complex engineering problems in a regulated environment. End-to-end ownership. Be...SeniorMedical device
$30 - $38 per hour
...startup environment in Plymouth, MN. This role focuses on regulated medical device manufacturing and involves close collaboration with cross-functional... ...support manufacturing operations and process improvements.Manage and maintain manufacturing equipment, including...SeniorMedical deviceContract workTemporary workMonday to FridayDay shift- ...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... ...devices, with strong negotiation and project management skills and collaboration across cross-...SeniorMedical deviceWorldwide
- ...Senior Buyer We believe that great healthcare is an essential safeguard... ...This role analyzes MRP requirements, manages supplier order execution, and... ...related professional certification Medical device, life sciences, or other regulated manufacturing experience,...SeniorMedical device
$80k - $120k
...individual in this role assists with medical writing and regulatory... ...and international medical device regulations to ensure submission... ...skills with the ability to manage multiple priorities in a fast... ...accuracy. Pay Rate: $80-120k Seniority level Mid-Senior level Employment...SeniorMedical deviceFull timeWork at office- ...field actions, and audits while guiding cross-functional teams on regulatory requirements. You will apply deep knowledge of U.S. FDA regulations and international frameworks to ensure continuous compliance and drive process improvements across the organization. #J-18808-...SeniorMedical device
- Senior R&D Engineer - Medical Devicesð Are you passionate about designing products... ...with an innovative medical device organization seeking a... ...implementation in a highly regulated environment.What You'll DoAs... ...methodsCAD and Product Data Management (PDM) platforms such as...SeniorMedical deviceWorldwide
- ...Senior Quality Assurance Engineer The Senior... ...oversight to various software/system/hardware development... ...and report to the Manager, Quality Assurance,... ...' experience in IVD, Medical Device, or Biotechnology organization... ...US and International regulations and standards...SeniorMedical deviceLocal area
- ...to join our team! ABOUT THE ROLE Senior Operations Manager We are seeking a software QA engineer to validate ENvue... ...experience, with at least 5 years in medical device leadership. Preferred Experience... ...Six Sigma certification, NPI in regulated environments, and Class II/III...SeniorMedical device
$80k - $120k
A medical equipment company is seeking a Mid-Senior level Quality Assurance professional to assist with regulatory documentation and medical writing. The... ...regulatory requirements, and ensuring compliance with FDA regulations. Ideal candidates will have at least 3 years of...SeniorMedical deviceFull timeWork at office$150k - $205k
ABOUT INSPIRE MEDICAL SYSTEMSInspire is the first of its kind medical device designed to make a difference... ...for a highly skilled Software Verification Engineer... ...entrance and exit criteria.Manage issues found during... ...and results reports for regulated software...Medical deviceWork experience placementLocal areaFlexible hoursShift work- ...product development and lifecycle activities in a regulated environment. This role is responsible for... ...customer requirements, with a strong focus on risk management, design controls, and compliance. Candidates with medical device experience are highly preferred; however,...SeniorMedical deviceWork at office
$93.6k - $131.04k
...Senior Firmware Test EngineerMinneapolis, MinnesotaAt Tactile Medical, we specialize in developing at-home therapy devices to treat lymphedema, chronic... ...help patients manage chronic health... ...firmware and device software test experience to help ensure regulated medical device...SeniorMedical deviceHourly pay- ...Software Project ManagerHistoSonics is a commercial-... ...multiple disease states and medical specialties.We offer... ...)The Software Project Manager leads the planning,... ...management experience in a regulated industry; preferably... ...applicable to medical device software, including...Medical deviceFull timeTemporary workVisa sponsorship
$100k - $130k
...Our client is a pioneering medical technology organization advancing... ...role combines advanced software engineering with compliance... ...practices within a highly regulated medical device environment. The successful... .... Participate in risk management activities including hazard...SeniorMedical deviceFlexible hours- ...Senior Systems Engineer Job Location: Plymouth... ...Have Skills/Attributes: Medical device, Product Development,... ...); Medical Device or Regulated Product Development (... ...Requirements & Risk Management (3+ yrs); Cross-... ...Bachelor's in Electrical, Software, Mechanical,...SeniorMedical deviceHourly payFull timeTemporary workShift work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Software Manager, Regulated Medical Devices. Be the first to apply!
- director of software Minneapolis, MN
- senior software manager Minneapolis, MN
- software manager Minneapolis, MN
- senior applications manager Minneapolis, MN
- application engineering manager Minneapolis, MN
- application manager Minneapolis, MN
- senior software development manager Minneapolis, MN
- director software engineering Minneapolis, MN
- IT software development manager Minneapolis, MN
- srs distribution Minneapolis, MN

