Medical Device Project Analyst - Data & Compliance (Hybrid)
Pharmavise Corporation
A leading medical device company is seeking a Project Specialist II for their Interventional Spine Team in Maple Grove, MN. This role involves managing vendor processes, leading market research, and generating data analytics from Salesforce and Tableau. The ideal candidate has a bachelor's degree, experience in market research, and advanced PowerPoint skills. This hybrid position requires 3 days onsite per week. Join us to make a meaningful impact in patient health and safety. #J-18808-Ljbffr Pharmavise Corporation
- ...A leading medical device company is seeking a Project Specialist II for their Interventional Spine Team in Maple... ...leading market research, and generating data analytics from Salesforce and... ...and advanced PowerPoint skills. This hybrid position requires 3 days onsite per...Medical device3 days per week
- ...firm is seeking a Quality Engineer for a hybrid role in Maple Grove, MN. This mid-... ...design history documentation, and ensuring compliance with regulatory standards. The ideal... ...design quality assurance, particularly in medical device development. Strong communication and...Medical device
- ...design controls, risk management, and quality systems for a medical device in a hybrid work setting. You will collaborate with cross-functional... ...maintain DHF, perform V&V, and lead continuous improvement in compliance and product lifecycle. This role requires a BS in...Medical deviceLocal area
- Project Specialist II — Medical Device (Hybrid — Maple Grove, MN) Possible Temp-to-Hire Maple Grove... ...solutions to complex compliance issues. We collaborate... ...This dual-role position (Analyst / Project Specialist) is... ...priorities in a fast-paced, data-driven environment. Key...Medical deviceTemporary work3 days per week
- A leading medical device company in Maple Grove, MN is seeking a Marketing... ...expertise in industry compliance. The role demands at least 2... ...medical device sector and strong project management skills. You'll be... ...is a contract position with hybrid flexibility. #J-18808-Ljbffr...Medical deviceContract work
- Marketing Communications Specialist II — Medical Device (Hybrid — Arbor Lakes, MN) Possible Temp-to-... ...to ensure the highest level of compliance, performance and efficiency. Supports... ...efficient compliance to LAR process. Project manage various processes with cross-functional...Medical deviceContract workTemporary work
- ...Senior Software Business Analyst Our Fortune 500 Medical Device client has an exciting opportunity for a Senior... ...understanding of regulatory and compliance requirements specific to healthcare... ...8:00 AM - 04:30 PM CST Work Setup: Hybrid at Maple Grove, MN Contract Length:...Medical deviceContract work
- ...is seeking a Design Assurance Engineer in Maple Grove, MN. This hybrid role requires expertise in quality systems and design control,... ...The position involves collaborating within cross-functional teams to ensure product safety and compliance. #J-18808-Ljbffr REQ SolutionsMedical device
- A medical device company in Maple Grove, MN is seeking a Sustaining Systems Design Quality Engineer II to ensure product safety and compliance. This hybrid role involves managing design change projects and working with cross-functional teams. Required qualifications include...Medical deviceFull timeContract workRemote work
- ...and managing submissions for Class II medical devices, ensuring compliance with both US and EU regulations. The ideal... ...7 years of relevant experience, with proven project management and technical writing skills. The position follows a hybrid work model. #J-18808-Ljbffr...Medical device
- ...A global medical technology leader is seeking a Principal Regulatory... ...role, you will review and ensure compliance of advertising and promotional materials for medical devices. The position requires a... ...feedback. This role follows a hybrid work model, requiring onsite presence...Medical device3 days per week
- ...in Maple Grove, Minnesota, is seeking a qualified Quality Assurance Specialist to ensure production and process control compliance in medical device manufacturing. Responsibilities include monitoring production staff, performing Device History Record reviews, and providing...Medical device
- Integrated Resources, Inc (IRI) is seeking a Recruiter for a hybrid position based in Maple Grove, MN. This role involves high-volume recruiting for Medical Assembler positions, where the candidate will develop sourcing strategies, conduct structured interviews, and prepare...Medical deviceContract workTemporary work
- Medical Engineering Consultants (MEC) seeks a Mid-Level Quality Engineer on a contract basis to support design assurance for the TheraSphere... ...-functional teams to ensure safety, quality, and regulatory compliance by reviewing design control deliverables and maintaining risk...Medical deviceContract work
- ...Design History File (DHF) Remediation activities for sustaining medical device products. Perform gap assessments, evidence collection,... ...documentation. Support audit/inspection readiness and regulatory compliance. Collaborate with R&D, Manufacturing, Regulatory Affairs (...Medical device
- ...submissions to FDA and EU, supporting new product development and compliance. The ideal candidate will have at least 7 years of experience... ...a Bachelor's degree in a scientific or engineering field. A hybrid work model is offered, requiring in-office attendance three days...Medical deviceWork at office3 days per week
- ...documenting processes, managing nonconformances, and supporting compliance with regulatory standards. Candidates should have a Bachelor's Degree in life sciences and significant experience in medical device development. Benefits include health care plans, retirement...Medical device
$102.1k - $194k
...Maple Grove, Minnesota (US-MN) Work model: Hybrid – employees are required to work in the... ...transfers and continuous improvement projects. Develop U.S. and EU regulatory... ...strategies and prepare submissions for Class II medical devices. Create innovative regulatory pathways...Medical deviceWork at officeLocal areaOverseas3 days per week$35 - $37 per hour
Data Analyst Contract role located in Maple Grove, MN (Hybrid). Rate Range $35/hour to $37/hour, negotiable... ...annotate, and prepare medical images to support... ...and clinicians. Ensure compliance with data governance standards... ...life‑changing medical devices through data‑driven...Medical deviceHourly payContract workTemporary workInternshipLocal area$74k - $106k
...our Plymouth, MN or Boston, MA office on a hybrid schedule. This job is responsible for... ...support to the actuarial function through data gathering, data analysis. and data presentation... ...but not limited to: Comprehensive medical, dental and vision insurance with no waiting...Full timeWork at officeFlexible hours- ...Maple Grove, MN. This hybrid role supports design quality assurance for medical electrical equipment/systems... ...product safety, compliance, and continuous improvement... ...manage design change projects including scoping, assessment... ...within the medical device industry. Strong...Medical deviceFull timeContract workRemote work
- ...the office and collaboration across Finance, Underwriting, and Product Development teams. The role supports financial modeling and data analysis, with opportunities to advance through actuarial exams and professional development within a collaborative, data-driven environment...Work at office3 days per week
- ...office. This role will create and update labeling and product information for medical devices, manage data, and drive the labeling change process to support patient safety and regulatory compliance. The candidate will collaborate with Regulatory Affairs, Quality, R&D,...Medical deviceWork at office
- ...passion for cutting‑edge medical technologies, join our... ...the life: The Senior Compliance Specialist plays a critical... ...Monitor complaint data to identify trends, potential... ...office conditions – hybrid work environment... ...background in medical devices, healthcare or a related...Medical deviceWork at officeLocal areaFlexible hours
$102.1k
...training materials for medical devices used in interventional... ...position follows a hybrid work model requiring employees... ...edits to strengthen compliance while supporting... ...statements, testimonials and data visualizations for... ...to manage multiple projects and meet deadlines in...Medical deviceWork at officeLocal area3 days per week- ...Global Trade Compliance Director Work mode: Hybrid Onsite Location(s): Quincy, MA, US, 02171 Additional Location... ..., maintenance and governance of data supporting free trade agreement... ...regulated industry, such as medical device, pharmaceutical, aerospace or a similar...Medical deviceWork at officeLocal areaRelocationRelocation package3 days per week
- ...product development and ongoing compliance for a broad ablation... ...synergy. This role follows a hybrid work model requiring employees... ...and continuous improvement projects.Develop U.S. and EU regulatory... ...prepare submissions for Class II medical devices.Create innovative regulatory...Medical deviceHourly payWork at officeLocal areaWorldwideShift work3 days per week
- ...Clinical monitoring Field clinical education Global regulatory compliance Clinical trial management within the medical device industry Roles in Clinical & Regulatory Affairs include: Clinical Project Manager Clinical Research Associate Clinical Research Scientist...Medical deviceTemporary workLocal areaWorldwideFlexible hours
- ...Production And Process Control Compliance This position is responsible for ensuring production and process control compliance during the development and manufacturing of medical devices at the Nextern Maple Grove facility. This position may also involve quality assurance...Medical device
- ...collaboration and innovation, offering a competitive compensation package, health and wellness benefits, and career development opportunities. Candidates with experience in Class III medical devices are especially encouraged to apply. #J-18808-Ljbffr Anteris TechnologiesMedical device
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