Senior Program Manager - Regulated Medical Devices
Integer Holdings
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 requirements are met. The role requires strong leadership, communication, and problem‑solving skills, with travel as needed to support customers and sites. Applicants with FDA/ISO regulatory exposure are preferred. #J-18808-Ljbffr Integer Holdings
- ...manufacturing driving innovation in the medical device industry. With rapid expansion across... ...part of something bigger. The Senior Program Manager is responsible for the successful... ...Field and 15 years or more experience in regulated industry such as Pharmaceuticals or...SeniorMedical deviceFull timeFlexible hours
$150k - $165k
...which makes everything possible.The Senior Program Manager, Plasmid DNA is responsible for leading... ...preference for 5+ years in a GMP-regulated CDMO environmentExperience managing programs... ...biotechnology, pharmaceutical, or medical device related field requiredWorking...SeniorMedical deviceFull timeRemote workWork from homeFlexible hoursNight shift$180k - $220k
ABOUT INSPIRE MEDICAL SYSTEMSInspire is the first of its kind medical device designed to make a difference in the lives... ...experienced and highly strategic Senior Program Manager to lead the cross-functional... ...applicable standards and regulations such as:FDA Design Controls2...SeniorMedical deviceWork experience placementLocal areaFlexible hours$171.2k - $256.8k
...developing innovative medical technologies that... ...therapies that help patients manage conditions affecting... ...position. The Senior Engineering Program Manager serves as the... ...working within regulated industries and quality... ...operations lead for medical device product development...SeniorMedical deviceFull timeContract workH1bWork at officeLocal areaImmediate startFlexible hours- ...manufacturing transfers. Manage external contractors and... ...client and Freudenberg Medical. Identify and recommend... ...experience in the medical device field. 6 - 10 years’ experience in a program manager position for a... ...oral and written) both to senior management, customers...SeniorMedical deviceContract workFor contractors
- Actalent is seeking a Software Test Engineer in Plymouth, MN, to execute system-level verification for a regulated medical device platform. The role involves hands-on testing on embedded hardware, script authoring, and audit-ready documentation within a DHF framework....Medical device
- ...is responsible for evaluating the safety and compatibility of medical devices with biological systems. The role involves planning and... ...please confirm your top 3 skills sets required? Experience in a regulated industry. Knowledge of international and domestic regulations...SeniorMedical device
- ...verification and validation of embedded medical systems, including execution... ...and safety in a highly regulated healthcare environment.... ...testing for embedded medical devices Execute regression, exploratory... ...and track defects in defect management systems Analyze failures, reproduce...SeniorMedical device
- ...in everyday technology devices from smartphones to... ...and commercialization programs that advance strategic... ...compliant, and manufacturable medical device solutions from... ..., ensuring proactive management of program performance... ...programs within a regulated industry. Demonstrated...Medical deviceContract work
$108k - $150k
...Clinical Science & Office of Medical Affairs team . This... ...for driving and managing clinical documentation... ...position will comply with regulations and ensure clinical... ...Develop and deliver medical device technical documents... ...Initiated Study Program (IISP) as assigned...Medical deviceWork at officeImmediate startFlexible hoursShift work- ...IEC design control procedures, regulations and standards Use various software tools and programs to complete the above... ...discipline Prior experience in medical devices, preferably for intensive care... ...SysML or UML) and requirement management tools Knowledge of DOORS and...SeniorMedical deviceShift work
- ...manufacturing. Our projects span medical devices, industrial automation,... ...boundaries. The Senior Engineering Project Manager is responsible for overseeing... ...out and advocate for programs in alignment with the... ...FAR (Federal Acquisition Regulation) and other government regulations...SeniorMedical deviceContract workFor subcontractor
- ...The Senior Process Engineer will lead the development, validation, optimization,... ...of manufacturing processes within a regulated medical device environment. This role partners with... ...Strong analytical, communication, project management, and problem-solving skills....SeniorMedical deviceWork at office
$36 - $40 per hour
...Senior Maintenance TechnicianManpower Engineering is partnering with a leader in medical device manufacturing for a Senior Maintenance Technician... ...dispositionFollow all relevant safety regulations and promote a positive... ...sponsored wellness programs and mental health...SeniorMedical deviceImmediate startFlexible hoursShift workDay shift$100k - $140k
Software Test Engineer / Senior Software Test Engineer / Principal... ...growing and innovative medical device organization is seeking Software... ...software used in highly regulated healthcare products, working... ...leadership for software quality programs.Define verification and...SeniorMedical device$115.5k - $169.4k
...is one of the largest medical device contract development... ..., and cardiac rhythm management markets. As a strategic... ...Administration (FDA) regulations, company policies and... ...impact on major programs. You may lead cross... ...is not an option. Senior Process Development Engineer...SeniorMedical deviceContract workImmediate start$210k - $290k
ABOUT INSPIRE MEDICAL SYSTEMSInspire is the first of its kind medical device designed to make a difference in the lives of those living with Obstructive... ...of our great team! POSITION SUMMARYThe Senior Director of Program Management, Commercial Patient Care Pathway will lead...SeniorMedical deviceWork experience placementLocal areaFlexible hours$105.87k - $158.8k
...Interventional Urology Senior Design Assurance... ...test protocols, manage test execution,... ...the stability test program Support and execute... ...laws and regulations, the MedTech Code... ...Wellness: Comprehensive medical, dental, and vision... ...s leading medical device companies. We are...SeniorMedical deviceContract workImmediate startFlexible hours$110k - $140k
...working with a rapidly growing medical device company developing... ...and they're looking to add a Senior Supplier Quality Engineer to... ...qualifications, and performance management activities * Drive supplier... ...aerospace, or other highly regulated manufacturing experience * Strong...SeniorMedical device$97.8k - $127.1k
Senior Programs Manager - Fire & Life Safety This position is based out of our Plymouth, MN office... ...policies, procedures, key objectives, and regulations. Our Ideal Candidate Ideally, this... ...health insurance options (medical, dental, and vision), a robust 401(k)...SeniorContract workFor contractorsWork experience placementFor subcontractorWork at officeLocal area$137k - $202k
...but not limited to: Quality Management Systems (QMS), Safety,... ...Drug Administration (FDA) regulations, company policies and operating... ...leadership, and guidance to project/program teams, serving as a member... ...product environment like medical devices, pharmaceuticals,...Medical deviceFull timeImmediate start- Senior Process Development Engineer - Medical Device ManufacturingWe're partnering with our client, an innovative medical device startup in Minneapolis, Minnesota... ...teams and third parties to execute IQ/OQ/PQ in a regulated environment.Automation & Tooling: Apply technical...SeniorMedical device
$205k
...below requirements for a Senior Systems Engineer to... ...with an established medical device company in the... ...requirements development, risk management activities,... ...devices or other highly regulated industriesFor senior-... ...product development programs is highly desiredLocation...SeniorMedical deviceWorldwideFlexible hours$107.2k - $160.8k
...developing innovative medical technologies that... ..., Clinical, Risk Management, and Post-Market... ...of projects.As a Senior Medical Safety Specialist... ..., medical device clinical practice,... ...federal and local regulations and may vary based... ...global well-being program).The following benefits...SeniorMedical deviceH1bWork at officeLocal areaImmediate startRemote workFlexible hours$117.75k - $172.7k
...lead technical discussions, manage new business opportunities and... ...Drug Administration (FDA) regulations, company policies and operating... ...opportunities and/or programs.o Leads technical discussions... ...component or assembly in the medical device industry. Prefer to have experience...SeniorMedical deviceFull timeImmediate start$145k - $200k
...the OpportunityAn innovative medical device organization is seeking a Senior Quality Manager to serve as the Quality Management... ...and Preventive Action (CAPA) programs as the site subject matter... ...understanding of medical device regulations and quality systems.Experience...SeniorMedical deviceFlexible hours- ...validation strategy and testing.Previous medical device experience with a history of... ...interfacesProduct Risk Assessment and Risk Management Experience (Fault Tree Analysis, Failure... ...systems to meet ISO and Quality System Regulation requirements, including IEC-60601-1, -...SeniorMedical deviceContract work
- ...Position Overview As a Senior Systems Engineer, you’... ...R&D team at Nonin Medical where your expertise will... ...innovation in medical device systems. In this role,... ...developing, documenting, and managing product requirements.... ...standards and regulations, specifically IEC 6060...SeniorMedical deviceFlexible hours
- ...on W2 Must-Have Skills: ~5+ years of Supplier Quality Engineering experience in a regulated industry (Medical Device preferred). ~ Supplier qualification, supplier management, and component qualification. ~ Strong problem-solving, communication, and technical...SeniorMedical device
$107.2k - $160.8k
...developing innovative medical technologies that... ..., Clinical, Risk Management, and Post-Market... ...projects. As a Senior Medical Safety Specialist... ..., medical device clinical practice,... ...federal and local regulations and may vary based... ...global well-being program). The following...SeniorMedical deviceFull timeH1bWork at officeLocal areaImmediate startRemote workFlexible hours
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