Project Manager - Medical Device - Dover, NH

The Project Manager is a key contributor in driving medical device manufacturing and product development projects from concept to completion. In this role you will provide hands-on support for designs of components, evaluate processes and tooling, ensure accurate process documentation, and strengthen project execution.

Client Details

My client is a leading contract manufacture in the Medical Device Manufacturing industry. They offer a collaborative work environment, diverse technical challenges, and strong opportunities for professional growth in a rapidly expanding industry.

Description

The Project Manager will:

• Lead and manage new product development and manufacturing transfer projects from initiation through production.
• Design products and tooling using SolidWorks and other CAD tools.
• Act as the primary point of contact between internal teams and customers to ensure alignment on project goals and timelines.
• Create and maintain detailed project documentation including schedules, budgets, resource plans, and risk assessments.
• Coordinate cross-functional efforts across R&D, Quality, Regulatory, Manufacturing, Marketing, and Supply Chain.
• Oversee the launch of new production lines, including procedure development, line clearance, and operator training.
• Provide hands-on support for manufacturing processes and ensure compliance with FDA QSR and ISO 13485 standards.
• Ensure accurate completion of Work Orders and manufacturing documentation per work instructions.
• Support validation activities such as IQ/OQ/PQ/PPQ, TMV, and process characterization.
• Drive continuous improvement in project execution, documentation, and quality systems.
• Mentor junior engineers and contribute to team development in project management and engineering practices.
• Identify cost-saving initiatives through process optimization, automation, and lean manufacturing.
• Promote and ensure compliance with environmental, health, and safety (EHS) standards.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

Profile

A successful Project Manager should have the following qualifications:

• Bachelor's degree in Mechanical, Biomedical, Materials Science, or related engineering field.
• Minimum 6 years of experience in regulated medical device manufacturing or product development.
• Demonstrated success in managing complex projects or programs.
• Proficiency in Microsoft Office and project management tools.
• Skilled in SolidWorks and other design technologies.
• Strong organizational, documentation, and communication abilities.
• Knowledge of FDA regulations, ISO 13485, and GMP standards.

Job Offer

• Competitive compensation
• Comprehensive benefits package
• Opportunities for professional growth and development
• Supportive company culture that values innovation and collaboration.
• Paid time off and other perks to maintain work-life balance.

If you're ready to take the next step in your career and contribute to impactful projects, apply now!

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.