Project Manager – Medical Device Manufacturing

Job description

Schedule:

Monday - Friday, 7:00 AM - 4:00 PM

About the company:

Our client is an industry leader in precision medical device manufacturing, specializing in small, high-precision components such as valves and connectors. They are a mission-driven company focused on quality, innovation, and customer success. The team operates in a state-of-the-art facility with a strong culture of teamwork and professional growth.

About the Role:

We are looking for a client-facing Project Manager to oversee medical device manufacturing projects, ensuring smooth communication between clients, manufacturing teams, tool makers, and machinists. The right candidate will have a strong technical background in mechanical engineering and be able to translate customer requirements into actionable production plans. This role requires a high level of organization, interpersonal skills, and technical expertise to ensure customer satisfaction and production efficiency.

Key Responsibilities:
  • Serve as the primary point of contact for clients, understanding their needs and expectations.
  • Communicate technical requirements to the manufacturing team, including tool makers and machinists.
  • Collaborate with engineering, production, and quality teams to ensure smooth project execution.
  • Manage project timelines, budgets, and deliverables to ensure successful outcomes.
  • Develop and maintain strong client relationships, providing updates and addressing concerns proactively.
  • Ensure projects align with medical device manufacturing standards and regulatory compliance.
  • Identify process improvements to enhance efficiency, quality, and cost-effectiveness

Qualifications & Skills:
  • Bachelor’s degree in Mechanical Engineering or related field.
  • 3+ years of experience in project management within a manufacturing or engineering environment (preferably medical device).
  • Ability to interpret technical drawings and communicate requirements effectively.
  • Strong client relationship management and communication skills.
  • Highly organized, detail-oriented, and skilled at multitasking.
  • Experience working in ISO 13485 / FDA-regulated environments is a plus.

Why Join us?
  • Competitive compensation based on experience.
  • 401(k) with company match.
  • Comprehensive benefits package (medical, dental, vision, life insurance).
  • 10 paid holidays + PTO.
  • Opportunity to lead and impact critical projects in medical device manufacturing.
  • A collaborative, growth-focused work culture.

Sincera Talent Partners is dedicated to fostering a diverse and inclusive environment. We are proud to be an equal opportunity employer, and we only partner with companies that share our commitment to diversity, equity, and inclusion. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We are committed to creating a workplace that values and respects individuals from all backgrounds and experiences.

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