Program Manager, Medical Device CAPA & NPI Lead
Mindlance
A medical device company in Minneapolis seeks an experienced project manager to lead multiple projects within its Restorative Therapy Group. The successful candidate will apply extensive knowledge of CAPA and risk management to ensure compliance with regulations while managing risks, executing product development projects, and leading cross-functional teams. Strong leadership skills and a proven track record in project management are essential for delivering high-quality work on time and within budget. #J-18808-Ljbffr Mindlance
- ...CAPA design projects, risk managements , he/she should be a SME ( should have medical device projects) Responsible for project management... ...(RPE) Department. Lead several different... ...Product Introduction (NPI) and the CAPA Board... ...large-scale, complex program; execute Product...Medical device
- ...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, Manufacturing...Medical device
- ...re partnering with a growing medical device manufacturing team looking to... ...support new product development (NPI) efforts. This is a hands‑on... ...environment - the hiring manager is very hands‑on and open to... ...investigations (nonconformances, CAPAs, process issues) using...Medical device
- ...Services, LLC is seeking a Principal Regulatory Affairs Specialist to lead global post-market regulatory compliance for Interventional Cardiology and Vascular Therapies. You will oversee PIRs, CAPA programs, recalls, field actions, and audits while guiding cross-functional...Medical device
$135k - $145k
...The Technical Project Manager, Global Operations for... ...Global Operations projects/programs that deliver critical... ...technology transfer/NPI projects/programs,... ...years of experience in leading medium to large-scale... ...transfer projects in the Medical Device or Diagnostics...Medical deviceFull time$105k - $125k
...travelers, traceability records)Lead and update PFMEAs to ensure... ...cause and corrective actions (RCA/CAPA)Drive continuous improvement... ...initiativesSupport NPI builds and transition products... ...in manufacturing engineering (medical device or regulated industry preferred...Medical device$86.7k - $173.3k
Abbott is seeking a dynamic NPI Supply Chain Associate Project Manager to drive the launch of next-generation medical devices in Plymouth, MN. In this role, you will collaborate... ...and various employee perks, including health and wellness programs. #J-18808-Ljbffr abbottMedical device$115k - $155k
...Program ManagerResonetics is a global leader in advanced engineering... ..., driving innovation in the medical device industry. With rapid... ...something bigger.The Program Manager is responsible for the successful... ...procedures. The Program Manager will lead a cross-functional team...Medical deviceFlexible hours$129.3k - $258.7k
...spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and... ...2 Save student debt program, and FreeU education benefit... ...providing device and management solutions for treating... ...in review boards for CAPA, complaints, business...Medical deviceFor contractorsWorldwideShift work$113.6k - $170.4k
...— developing innovative medical technologies that improve... ...LifeJoin our Global Supply Management team as a Strategic Sourcing Program Manager for the Mergers &... ...risks. This role leads end-to-end integration planning... ...sourcing operations, medical devices, or related...Medical deviceFull timeContract workH1bWork at officeLocal areaImmediate startFlexible hours$113.6k - $170.4k
...— developing innovative medical technologies that improve... ...Join our Global Supply Management team as a Strategic Sourcing Program Manager for the Mergers &... ...managing risks. This role leads end-to-end integration planning... ...operations, medical devices, or related industry ~...Medical deviceFull timeContract workH1bWork at officeLocal areaImmediate startFlexible hours- ...Program ManagerThe Program Manager is responsible for leading medical device development programs within a dynamic, customer-focused environment. This role drives cross-functional execution from concept through production, ensuring alignment with customer requirements...Medical deviceTemporary work
- Integer is seeking a Senior Project Manager to lead end-to-end engineering projects in Minnesota, guiding initiatives from inception through implementation and handoff. You will coordinate with cross-functional teams, ensure adherence to budgets, schedules, and regulatory...Medical device
- ...Manufacturing Program Manager Our mid-sized medical device client is building a Program Management department. The Manufacturing Program Manager will oversee... ...establish a framework for oversight and management of NPI, Capacity Initiatives, and Transfer programs at...Medical device
- ...Distributed by APM) is seeking a driven sales representative in Minneapolis to join a rapidly growing medical device company redefining healthcare success. You will build and manage relationships with hospitals, surgery centers, and clinicians, educate decision-makers on...Medical device
- 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...Medical device
$24.66 - $30.19 per hour
Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted... ...The Cell Leader II will manage employee time, approve time... ...Operational Excellence Program Ability to cross train in...Medical deviceHourly payContract workTemporary workLocal areaMonday to FridayShift workAfternoon shift- Bracco Medical Technologies is seeking a Principal Regulatory Affairs Specialist to develop and execute regulatory strategies for medical device products across lifecycle changes. You’ll lead global submissions and provide on‑site regulatory support for 510(k), EU MDR,...Medical device
- ...Interventional Oncology and Embolization division. The role involves PIRs, CAPAs, recalls, audits and cross-functional collaboration in a... ...should have 5+ years in Regulatory Affairs/Quality for medical devices, knowledge of US and EU regulations, and strong technical writing...Medical device
- ...Johnson MedTech in Plymouth, MN seeks a Sr Program Lead, Regulatory Affairs to lead global regulatory strategies for medical devices and ensure timely commercialization in... ...devices, with strong negotiation and project management skills and collaboration across cross-functional...Medical deviceWorldwide
$80k - $200k
...industry cloud, is seeking an experienced consultant to lead MedTech Regulatory Information Management implementations. The role involves guiding... ...systems implementation experience, particularly within medical devices. The position offers the flexibility to work remotely...Medical deviceRemote job- Cretex Medical Component and Device Technologies in Minnesota seeks a Cell Lead II to coordinate and lead a cellular work team in a manufacturing setting. You will manage time, approve time transactions in ADP, and create performance goals aligned with company objectives...Medical deviceNight shift
$142.4k - $213.6k
...developing innovative medical technologies that improve... ...of new medical device products or software systems... ...to market release. Manages feasibility studies of... ...Practical experience leading and managing the execution... ...or global engineering programs. Familiarity with systems...Medical deviceH1bWork at officeLocal areaImmediate startWorldwideFlexible hours- Cretex Medical Component and Device Technologies is seeking a Cell Lead II in Minneapolis, MN. The role involves coordinating and leading the activities of a manufacturing team, focusing on production efficiency and quality. The ideal candidate will have supervisory experience...Medical deviceHourly payAfternoon shift
- ...Category team, the Category Lead is responsible for developing... ...role owns the strategic management of assigned categories, including... ..., supplier performance programs, and contract negotiations.... ...certification. Experience within medical device, life sciences, healthcare,...Medical deviceContract workFlexible hours
$24.66 - $30.19 per hour
...Job Description Job Description We are a leading medical device manufacturer specializing in high-quality molded products that improve patient... ...position is designed to help reduce supervisor workload by managing employee performance, engagement, and day-to-day personnel...Medical deviceHourly payWorldwideShift work$30 - $35 per hour
...Title : Quality Lead Location : St. Paul... ...-35/hr Industry : Medical Supplies About The... ...organization in the medical device and life sciences... ...’s Quality Management System (QMS). This... ...the QMS training program, including onboarding... ...actions (CAPAs). Ensure timely, compliant...Medical devicePermanent employmentTemporary workWork at officeFlexible hours- Incedo Inc. is seeking a Program Manager to lead a multi-workstream rebuild of the Business Banking BRH platform. You will coordinate with product, engineering, operations, risk, and branch leadership to deliver a modernized BRH ecosystem that improves branch efficiency...
$137k - $202k
...but not limited to: Quality Management Systems (QMS), Safety, Environmental... ..., and guidance to project/program teams, serving as a member... ...product environment like medical devices, pharmaceuticals, automotive... ...: Demonstrated ability to lead team activities Strong ability...Medical deviceWork at officeImmediate start- ...experience in FDA-regulated medical device manufacturing. Roles & Responsibilities... ...Plans, Nonconformance & CAPA. # Strong knowledge of ISO... ..., FDA 21 CFR Part 820 & Risk Management. # Customer complaint... ...# Manufacturing readiness, NPI & scale-up. # Strong technical...Medical deviceContract work
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