Job Summary:

The Vice President, Product Development’s role is to plan, develop, and implement strategy, policies, procedures, and practices for the Development function.

Essential Duties and Responsibilities: 

  • Lead engineering teams including electrical, firmware, software, automated test, and systems engineering, as well as external engineering partners.

  • Develop and implement development strategies to meet corporate goals and objectives.  

  • Collaborate with the Supply Chain, Program Management, Marketing, Manufacturing, Clinical, Regulatory, and Research & Science functions to determine new product development strategy from product inception to market launch.

  • Participate in the short and long-range planning of new product opportunities.

  • Recruit, hire, train, manage, mentor, and develop research and development staff members. 

  • Maintain a safe, clean, and QSR compliant facility.

  • Contribute to the overall intellectual property position of the company by aggressively encouraging and managing invention and patent applications.

  • Manage Design Review process.

  • Participate in the ongoing evaluation of potential markets, new products, and new business opportunities.

  • Plan, schedule, and complete projects in an aggressive manner consistent with corporate objectives.

  • Maintain superior knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to neuromodulation technology products.

  • Maintain regular contact with and gather feedback from key physicians involved in Presidio’s product development programs.

  • Regularly make presentations to senior management and Board of Directors.

  • Participate in executive meetings and planning sessions.

  • Develop and manage departmental budget. Establish quarterly spending strategies to maximize results while managing financial constraints.

  • Procure and oversee outside vendors and consultants as required.

  • Maintain QSR systems, including design control procedures, pre-clinical testing programs, and post production QSR compliance.  Provide support in the prompt resolution of product complaints and/or safety issues.

  • Proactively support company goals and objectives, policies and procedures, the Quality System Regulation, ISO/MDD regulations, and other regulatory requirements.

  • Maintain a professional and credible image with key physicians, consultants, suppliers, and co-workers.

  • Actively work to promote team building and morale within the department.

  • Perform other duties as assigned.

  • Comply with Presidio Medical’s quality system requirements as well as any applicable regulatory requirements.

  • Comply with all health and safety regulations, policies, and work practices.

  • Other duties as assigned.

Qualification Requirements: Experience

  • 15+ years related experience in the medical device industry, in addition to at least eight years management experience or equivalent.

  • Experience in neuromodulation, pain management or related field preferred. 

  • Results oriented with excellent analytical, strategic, business planning, communication, and teamwork/collaboration skills.

  • Strategic thinker who possesses both a solid business acumen and the ability to look beyond the current state and plan strategies that take into consideration the long-term business objectives and the external competitive and business environment.

  • Ability to simplify complex ideas/concepts, synthesize and summarize a complex set of facts and opportunities within the broader strategic context. 

  • Demonstrated ability to effectively communicate ideas and lead others to accomplish challenging goals and objectives. 

  • Demonstrated ability to build, lead, develop and mentor development team.

  • Ability to develop creative solutions to complex problems.

  • Adept at handling multiple projects and tight deadlines in a fast-paced environment.

  • Demonstrated ability to work as part of a team and manage initiatives that require collaboration across multiple functional areas.

  • A desire to be part of a highly innovative company aimed at transforming the lives of people with significant unmet medical needs.

Knowledge/skills/Abilities:

Required

  • Thorough working knowledge of the medical device industry is required as is the ability to exercise sound decision-making and good judgment consistent with a senior level position.

  • Excellent written and verbal communication skills. 

  • Excellent interpersonal skills and a spirit of teamwork.

Education:

  • Bachelor’s Degree in engineering is required. 

  • Master’s Degree is preferred.


Physical Demands:

  • Varied sitting, standing, and walking.

  • Ability to lift and carry 50lbs. or less.


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