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
- 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
- ...Minnetonka, MN office. This role involves conducting important data analyses, communicating effectively with third-party administrators... ...analytical and organizational skills. The position offers a hybrid work schedule, competitive pay, and a comprehensive benefits package...SuggestedWork at office
- ...and managing submissions for Class II medical devices, ensuring compliance with both US and EU regulations. The ideal... ...of relevant experience, with proven project management and technical writing skills. The position follows a hybrid work model. #J-18808-Ljbffr Boston...Medical device
- ...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
$65.8k - $125k
Boston Scientific Gruppe seeks a Product Analyst III based in Maple Grove, Minnesota. In... ...and manage regulatory submissions for medical devices. The position requires a Bachelor’s... ...skills are essential. This role follows a hybrid work model. Salary ranges from $65,800...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
$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- 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
- ...training materials for medical devices used in interventional... ...This role 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
- ...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
$137.7k
...Associate Director, Medical Affairs & Clinical Strategy Onsite... ...integrity of clinical data communication. This role is hybrid (3 days onsite) out of... ...pharmaceutical and/or medical device industry 25% domestic and... ...workplace safety in compliance with the applicable law....Medical deviceHourly payWork at officeShift work- ...Product Analyst III At Boston Scientific... ..., you'll write Medical Device Reports (MDR) and... ...III you'll ensure compliance with Good Manufacturing... ...role follows a hybrid work model... ...gathering sufficient data from clinical... ...divisional improvement projects. Provide...Medical deviceWork at officeLocal area3 days per week
$102.1k
...training materials for medical devices used in interventional... .... This role follows a hybrid work model requiring... ...actionable edits to strengthen compliance while supporting... ..., testimonials and data visualizations for cross... ...to manage multiple projects and meet deadlines in...Medical deviceHourly payWork at officeLocal areaShift 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
- ...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
- ...Our client, a growing medical device company, is seeking a Supplier Quality Engineer to support... ...activities and ensure the quality and compliance of externally sourced components and... ...Participate in supplier quality improvement projects. Support risk management and...Medical device
- ...IO&E division. In this position you will work with a cross-functional team to support the commercialized medical device and ensure the safety, quality and compliance of the product by reviewing and maintaining the design control deliverables and risk management...Medical deviceWork at officeRemote work
- Boston Scientific is hiring a Principal Regulatory Affairs Specialist in Maple Grove, MN, to lead regulatory strategy for a broad ablation portfolio. The role involves coordinating IDEs, 510(k)s, and EU MDR submissions, collaborating across R&D, Quality, Operations and ...Medical device
- ...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
- ...complex, clinically driven device programs. You will... .... This role follows a hybrid work model requiring... ...strategies that protect compliance, patient safety and... ...technologies, complex medical devices, clinical evidence... ...up to 20% to support project team collaboration,...Medical deviceWork at officeLocal areaNight shift3 days per week
- ...strategies, handling documentation for market authorizations, and ensuring adherence to compliance standards. The ideal candidate will have 2-5 years of experience in medical devices, strong analytical skills, and proficiency in Microsoft Office. Competitive...Medical deviceWork at office
$88k - $130k
...the product lifecycle and coordinating projects effectively. The role supports the Regulatory... ...changes to commercially distributed medical devices Conduct appropriate research to develop... ...promotional information for regulatory compliance Assist with SOP development and...Medical deviceTemporary workWork at officeFlexible hours- ...platform. Candidates should have at least 10 years of experience, particularly with FDA interactions for complex medical devices. The position operates under a hybrid model, requiring in-office presence three days a week, and offers opportunities for professional growth and...Medical deviceWork at office3 days per week
$65.8k
...role The Product Analyst III operates in a... ...III, you’ll write Medical Device Reports (MDR) and... ...3 you’ll ensure compliance with Good Manufacturing... ...role follows a hybrid work model... ...gathering sufficient data from clinical... ...divisional improvement projects. Provide support...Medical deviceHourly payWork at officeLocal areaRelocation packageShift work3 days per week$105k - $144k
...for an experienced Information Security Assurance Analyst to bolster cybersecurity governance and compliance efforts. You will protect critical systems, contribute... ...$105,000 - $144,000 annually and is eligible for a hybrid schedule in Maple Grove, MN. #J-18808-Ljbffr Duck...$113.03k - $165.77k
...within the United States and International markets and ensure compliance with relevant FDA, EU, ISO, and other regulatory requirements... .... Minimum Experience: 7+ years of US and International medical device regulatory submission/approval experience, to include FDA,...Medical deviceImmediate start$58.8k - $105k
...Advancement, access to data, variety of product... ...hospitals, pharmaceutical and medical device manufacturers, and... ..., AZ and will have a hybrid work arrangement model... ...This Actuarial Analyst position will be supporting... ...other market specific projects Perform pricing of new...Medical deviceMinimum wageFull timeWork experience placementInternshipJanuary startWork at officeLocal areaRelocation
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Medical Device Project Analyst - Data & Compliance (Hybrid). Be the first to apply!
- remote data analyst part time Maple Grove, MN
- medical device Maple Grove, MN
- special projects Maple Grove, MN
- projects Maple Grove, MN
- implementation project manager remote Maple Grove, MN
- software implementation project manager Maple Grove, MN
- senior implementation project manager Maple Grove, MN
- retail project merchandiser part time Maple Grove, MN
- project controls Maple Grove, MN
- project finance Maple Grove, MN

