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Program Manager - Medical Device

Job in Beverly, Essex County, Massachusetts, 01915, USA
Listing for: Freudenberg Medical
Full Time position
Listed on 2026-07-10
Job specializations:
  • Management
    Operations Management, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 120000 - 140000 USD Yearly USD 120000.00 140000.00 YEAR
Job Description & How to Apply Below

Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.

Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner, delivering high‑quality solutions from ideation and market launch to volume production for medical device and pharmaceutical companies. With proven expertise in materials and technologies, Freudenberg Medical offers an extensive range of vertically integrated capabilities: precision molding and extrusions, complex catheters, hypotubes, and coatings.

Benefits
  • 401K Match:
    Save for retirement with the company's help.
  • Diversity & Inclusion:
    We focus on providing an inclusive environment and recognize our diversity contributes to our success.
  • Sustainability & Social Commitment:
    We support social and sustainable projects and encourage employee involvement.
  • Corporate Events:
    We celebrate success as a team, because only together can we achieve our goals.
  • Personal Development:
    We offer a variety of trainings to ensure you can develop in your career.

* Candidates must be legally authorized to work in the United States without current or future visa sponsorship*

We offer a comprehensive benefits package that includes medical, dental, and vision coverage, retirement savings with company match and paid time‑off. Additional details will be shared during the recruitment process.

Locations:
Beverly, MA and Baldwin Park, CA (On‑Site). Freudenberg Medical LLC.

Expected salary range for this position is $120,000 to $140,000 annually, depending on skills, experience, and qualifications.

Responsibilities
  • Direct cross‑functional internal teams, external vendors, suppliers, and strategic partners; assess resource needs, utilization, and development. May manage direct reports. Build team ownership and commitment to projects and assign clear authority, accountability, and deliverables.
  • Drive all phases of the product development cycle, including feasibility, concept, validation, production transfer, and sustaining manufacturing, guide specification development, tooling, and test methodologies.
  • Develop and monitor project budgets, internal billing, and transfer cost of goods sold (TCOGS); communicate financial variances and negotiate adjustments with customers and stakeholders.
  • Maintain alignment with clinicians, customers, internal teams, and FM key stakeholders through timely updates, product deliverables, issue resolution, and structured project communications.
  • Identify constraints and risks, maintain credible schedules, align with CCPM/PCE practices, and ensure communication of updates to project timelines and along with any mitigation strategies.
  • Measure, report and improve program KPIs, demonstrate cost reduction through process optimization, and encourage positive behaviors and teamwork norms for high‑performance culture.
  • Develop and maintain compliant design/process documentation; oversee test and measurement fixture identification and ensure quality documentation for regulatory and operational readiness.
  • Mentor and support engineering staff development while fostering a high‑performing, collaborative project culture.
  • Oversee multiple related projects or a full customer program with business‑level accountability, using Program Management best practices through entire corporate PDP.
  • Managing efforts for compliance ensure design control, DMR/DHF compliance, risk analysis, and alignment with ISO standards, country‑specific (FDA, MDR, Health Canada, PMDA, etc.), GMP regulations, and customer requirements.
  • Provide technical and project‑management leadership, set priorities, allocate tasks, mentor team members, and foster a culture of efficiency, innovation, and regulatory excellence across the organization.
  • Evaluate new business opportunities and lead quoting and proposal development and collaborate with Sales to close deals aligned with strategic goals.
  • Maintain project documentation in line with internal procedures and…
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