Research & Development Project Manager - Minneapolis, United States - Vital Path

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    Description
    Join VitalPath in New Hope as a Research & Development Project Manager
    About VitalPath

    VitalPath is a trusted partner in the catheter design and manufacturing of custom medical devices that save lives and restore patient health and vital function.

    Were excited about this important work and bring vital energy to our customer partnerships.

    In our growing organization its important that we continue to offer a small-company, family-oriented environment with competitive pay and benefits.

    If you want to make a difference in peoples lives and be a part of a friendly, fun place to work with people that value diversity, come join our team
    About the Position
    The Research & Development (R&D) Project Manager will be responsible for leading development projects.

    This position will serve as the primary customer contact throughout the duration of the project, act as a key technical team member while also driving a cross-functional team to successfully meet project requirement on schedule and within budget.

    This position is responsible for ensuring that all deliverables within the scope of the project are completed in accordance with VitalPaths Quality Management System (QMS) and are compliant with FDA QSR (21 CFR 820), and applicable ISO 13485 requirements.

    Responsibilities
    Manage the scope, schedule and budget of moderate complexity, technically challenging customer facing projects based on the definition of agreed upon customer quotes/proposals
    Effectively manage multiple projects and customers, generally of medium size and complexity
    Establish and maintain excellent customer relationships through regular communication including but not limited to reoccurring project meetings, project health reports and emailed status updates
    Identify creative opportunities to add value to individual customers programs and products and provide value for VitalPath, beyond defined project scope and constraints when necessary
    Partner with business development in evaluating new project opportunities, including defining realistic project requirements to support the development of accurate quotes/proposals
    Participate in technical design reviews and phase reviews
    Identify project and business risks and define and implement agreed upon risk mitigation plans
    Ensure compliance with Product Development Process in accordance with internal and customer Quality Management Systems (QMS)
    Drive the impeccable documentation of design control documents and project decisions to create comprehensive Design History Files for projects
    Serve as an additional technical, engineering resource for projects as required; Mitigate project risk by identifying and proposing solutions to technical challenges
    Collaborate with management to execute resources planning and communicate expected revenue targets based on project goals and schedules
    Other duties as assigned
    Requirements
    Bachelors Degree in relevant engineering or other technical discipline required
    Minimum 5 years experience in product development of relevant medical devices and 1 year of project leadership
    Demonstrated ability to communicate complex technical ideas in a concise and effective manner, both written and verbally, to internal and external project stakeholders
    Working knowledge of minimally invasive medical device design, development, and manufacturing processes
    Strong interpersonal skills and ability to lead and motivate team members who are not direct reports
    Experience with project management methodologies and tools including schedule, budget, and resource management techniques
    Proficient with Microsoft Office programs including Word, Excel, PowerPoint, Outlook, and Teams
    Must be able to sit/stand for an extended period of time
    Preferred
    Bachelors Degree in Plastics, Biomedical or Mechanical Engineering preferred
    Demonstrated track record of leading high performing technical teams working on the development of complex medical devices
    Working knowledge of design control and both FDA and ISO regulations
    Formal project management experience
    Experience managing projects through all phases of the product life cycle from initial concept through transfer to manufacturing
    Experience with Microsoft Project or similar software
    Willingness to travel up to 15%
    Benefits
    Comprehensive, Low Cost Health and Dental Insurance Plans Available
    Vision Insurance
    Health Savings Account with company contribution
    Short and Long Term Disability
    Supplemental insurances (short term disability, AD&D, life insurance, and more)
    Paid Time Off
    Paid Holidays
    401K with company match
    Competitive compensation
    Opportunities for career growth and advancement

    VitalPath is an Equal Opportunity Employer.

    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, work related mental or physical disability, veteran status, sexual orientation, gender identity, or genetic information.

    VitalPath participates in E-Verify.
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