More jobs:
Program Manager
Job in
Beverly, Essex County, Massachusetts, 01915, USA
Listed on 2025-12-31
Listing for:
Freudenberg Medical
Full Time
position Listed on 2025-12-31
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below
Join to apply for the Program Manager role at Freudenberg Medical
.
Beverly, MA – On‑Site.
Expected salary range: $115,000 to $150,000 annually, depending on skills, experience, and qualifications.
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. - Personal Development:
We offer a variety of trainings to ensure you can develop in your career. - 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. - * NO VISA Sponsorship*
- 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.
- Oversees 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 notified‑body expectations, supporting audits and ensuring robust change‑control and traceability. Prepare reports and project summaries to communicate the status of projects on a regular basis.
- Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field.
- 8+ years’ experience in Medical Device or related industry.
- 6+ years’ experience in Project/Program Management in a manufacturing environment, with advanced experience of leading work within a project plan framework, including managing a schedule, budget, scope, progress, reporting, and prototyping through product launch.
- Prior experience with silicone material, plastics, and/or extrusions.
- In‑depth understanding of engineering and manufacturing processes used in medical device production, such as engineering drawings, running equipment, injection molding, extrusion, catheter manufacturing, and assembly, including the materials used.
- Advanced experience with engineering/statistical problem‑solving methodologies (including Design of Experiments [DOE]), critical thinking, and…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×