Medical Device Project Leader: NPD & Regulatory
CAIRE Inc
MGC Diagnostics is seeking a skilled Project Manager to lead the development of cardiorespiratory diagnostic medical devices. This role oversees cross-functional teams across locations, from concept through global commercialization, and supports engagement with external partners to meet regulatory and quality standards. The successful candidate will drive stage-gate development in a regulated environment, manage schedules, budgets, and KPIs, and deliver regular updates to leadership while
#J-18808-Ljbffr- ...Katalyst CRO is seeking a results-driven Project Manager to support CIA initiatives in a fast-paced medical device environment. You will lead cross-functional teams,... ...equivalent certification is a plus, and the role requires compliance with regulatory standards #J-18808-LjbffrRegulatoryMedical device
- ...Binks US LLC in Shoreview, MN is seeking an NPD Project Manager to lead new product development from conception through completion. This... ...teams, manages scope, schedule and budget, and ensures regulatory and engineering standards are met. The role focuses on planning...RegulatoryFull time
$95.9k - $129.47k
...True to Life, by advancing medical technologies and... ...development and management of projects for New Product Development (NPD). The Product Quality Engineer... ...procedures and medical device regulations. The Product... ...Preventative Actions, and regulatory requirements such as FDA...RegulatoryMedical deviceFull timeLocal areaWorldwideFlexible hours$124.7k - $187k
...Master’s + 5 years) of medical device experience, with a... ...new product development projects. We are seeking a Staff... ...Product Development (NPD) programs.In this high... ...efforts to meet strict regulatory and quality standards.... ...industrial technology leader creating a safer, sustainable...RegulatoryMedical deviceLocal area$117k - $125k
...seeking a skilled and driven Project Manager to lead the... ...cardiorespiratory diagnostic medical devices. This role is responsible for... ...ensuring compliance with global regulatory and quality standards. Essential... ...of new product development (NPD) for Class II FDA-regulated...RegulatoryMedical deviceFull timeContract workLocal area- Experis Technology Group is seeking a Project Engineer - Sustaining Engineering in Plymouth, MN. You will lead sustaining and design... ...cross-functional teams across Engineering, Operations, Quality, Regulatory, and Supply Chain to ensure regulatory and quality system...RegulatoryMedical deviceContract work
- Kelly Services, Inc. - - Responsibilities: Assemble and test medical devices; Collaborate with Manufacturing Lead to meet production... ...Report quality or process issues; Maintain clean, organized, and safe work area; Follow regulatory and quality system requirementsRegulatoryMedical device
- ...role requires 5+ years in manufacturing operations, strong leadership, and a data-driven approach to achieve efficiency, cost reduction, and superior quality. A manufacturing/medical device background is preferred, with a focus on regulatory compliance #J-18808-LjbffrRegulatoryMedical device
- ...contract focused on post-market complaint investigations across ICVT devices. You will analyze surveillance data, lead root-cause... ...collaborate cross-functionally to improve CIS processes and ensure regulatory compliance. Responsibilities include presenting findings to...RegulatoryMedical deviceContract work
- ...III for a 12-month, 100% onsite assignment. The role focuses on integrating quality processes for medical devices, with pay of $45/hour on W2. You will support regulatory compliance (FDA/ISO 13485, 14971), risk management, and documentation such as VMPs, DIRA, and inspection...RegulatoryMedical device
- Actalent in Minnesota seeks a Medical Device Laboratory Technician to join a high-performance team. The role involves routine particulate... ...assist in audit readiness while maintaining compliance with regulatory standards. The ideal candidate has an AA degree or equivalent...RegulatoryMedical device
- Actalent seeks a Labeling Specialist to develop and manage medical device labeling using BarTender in a regulated environment. You will own... ..., author labeling content, and collaborate with packaging, regulatory, QA, and document control to ensure regulatory and packaging...RegulatoryMedical device
- ...Abbott Vascular Devices PositionThis position works out of our St... ...the production of high quality medical device hardware and systems.... ...Management Systems (EMS), and other regulatory requirements.• Complies with... ...engage others to accomplish projects. Strong verbal and written...RegulatoryMedical deviceFor contractors
- ...delivering innovative solutions in the medical device industry. Must Have Previous experience... ...Knowledgeable on Medical Device Regulatory Requirements Experience with Quality... .... Formulates, delivers, and/or manages projects assigned and works with other stakeholders...RegulatoryMedical device
$30 per hour
Our client, a medical device technology organization, is seeking an Entry Level Medical Device... ...relevant internships, laboratory, or project experience are encouraged). Strong foundation... ..., Mechanical, Systems, Quality, and Regulatory Engineering. Develop stronger...RegulatoryMedical deviceInternship- ...commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide... ...technical expertise in Quality, Regulatory Compliance and Manufacturing Science... ...Supply Chain, and Marketing to ensure project success. Identifies and implements improvements...RegulatoryMedical deviceContract workTemporary workDay shift
- ...Regulation (QSR 21 CFR 820), Canadian Medical Device Regulation (CMDR), EU Medical... ...release readiness. Support project deliverables, supply risk... ...to New Product Development (NPD) working in partnership with... ...industry standards, regulatory requirements, and customer requirements...RegulatoryMedical device
- Quality Engineer I — Medical Device (Onsite — Arden Hills, MN) Possible Contract Extension Saint Paul, United States | Posted on 04/20/20... ...with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our...RegulatoryMedical deviceContract work
- ...manufacturing, risk assessments, and quality system activities. The role emphasizes risk-based decision-making and regulatory readiness within a regulated medical device environment. The candidate will collaborate with Manufacturing, Quality, Regulatory Affairs, and external...RegulatoryMedical deviceContract work
- ...Paralegal serves as Forj Medical's primary internal... ...insurance, product liability, regulatory compliance, and... ...with long-lead-time, project-based contracts (e.g.,... ...comfortable engaging senior leaders and a sales... ...experience in medical device, contract manufacturing...RegulatoryMedical deviceContract workWork at officeLocal area
- ...Quality Engineering experience in a regulated industry (Medical Device preferred). ~ Supplier qualification, supplier... ...Control Plans, and receiving inspection. ~ Knowledge of NPD, quality systems, and regulatory requirements. Key Responsibilities: Qualify and...RegulatoryMedical device
$18.75 per hour
...Medical AssemblerLocation: St. Paul, MN1st shift: 7am-3:30pm, M-FPay Rate: $18.75 per hourResponsibilitiesEnsure... ...and utilize appropriate safety devices when performing all... ...Environmental Management Systems (EMS), and other regulatory requirementsRequired Qualifications6...RegulatoryMedical deviceShift work- ...experience in materials engineering, preferably within a regulated medical device environment. Materials Behavior & Failure Analysis:... ...experience with standard materials characterization lab methods. Regulatory Knowledge: Deep understanding of domestic and international...RegulatoryMedical device
- ...processes to improve accuracy, efficiency, and on-time delivery. The role is on-site in Woodbury, MN, with responsibilities spanning domestic and international shipping, RMA handling, and collaboration with Quality and Finance to meet regulatory requirements. #J-18808-LjbffrRegulatoryMedical device
- ...works across manufacturing, engineering, regulatory affairs, and supplier quality teams to... ...supporting quality systems within the medical device, pharmaceutical, biotechnology, or combination... ...review, organizational, and project prioritization skills.Ability to travel...RegulatoryMedical device
- ...controls processes, ensuring compliance to Medical Device regulations and BSC Quality System... ...include:Leadership of cross functional project teamsProviding continuous and rigorous... ...experienceMedical device manufacturing, quality or regulatory/compliance environmentPrevious...RegulatoryMedical deviceWork at officeLocal areaRelocation package3 days per week
$32 - $34 per hour
...Approximately half of their time will be spent on project work, 20% on meetings and documentation... ...with cross-functional teams and regulatory groups. During the first 90 days,... ...are looking for a recent grad. Medical device or pharmaceutical industry experience is...RegulatoryMedical deviceWork at office- ...support for contract manufactured devices, acquisition activities, new product development projects, microbiological risk... ...Manufacturing, Quality, Supplier Quality, Regulatory Affairs, Research &... ...Preferred Qualifications Medical device industry experience strongly...RegulatoryMedical deviceContract workShift workDay shift
$59 per hour
...Industry: Medical Device / Life Sciences Pay Rate: Up to $59.00 per hour Travel: Approximately... ..., Quality, Supplier Quality, Regulatory Affairs, Research & Development, and external... ...integration, and manufacturing transfer projects. Collaborate with Engineering, Manufacturing...RegulatoryMedical deviceHourly payContract work- ...experience in design and development of Medical Devices Software systems using C/C++, J2EE or .... ...knowledge of FDA and other Medical regulatory submission requirements • At least 4 years... ...and driving an independent project from an architectural standpoint. • At...RegulatoryMedical device
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