Senior Program Manager - Medical Devices

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.

Some of your 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.

Performance Related Bonus: When you have an impact, you can reap the rewards.

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.

*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.

Minnetonka, MN

Jeffersonville, IN

On-Site

Freudenberg Medical LLC

payments The expected salary range for this position is $110,000 to $150,000 annually, depending on skills, experience, and qualifications.

You support our team as

Senior Program Manager - Medical Devices

Responsibilities

• Provide leadership, goal-setting, communications, and facilitation skills to guide and motivate project personnel in a matrixed environment.
• Be able to lead project teams on a variety of complex projects such as concept development, design and process development, design transfers, and manufacturing transfers.
• Manage external contractors and vendors to ensure completion of projects per the agreed upon milestones and within budget.
• Responsible for tracking, monitoring and managing project schedules.
• Track and manage project budget to plan and identify and improve processes to reduce costs.
• Identify and manage resolution of potential deviations from the quote/contract, Project Master Plan or other project documents along with performing and managing project risk relative to the client and Freudenberg Medical.
• Identify and recommend appropriate resource allocations from all areas to support the project requirements and monitor their utilization/efficiency.
• Manage billing/invoicing activities on a monthly basis and provide monthly revenue estimates.
• Work with manufacturing team to develop the transfer cost of goods sold (TCOGS).
• Communicate with clients on a regular basis (as required) and provide monthly updates to Freudenberg Medical Management.
• Document project and team meetings minutes and distribute to appropriate management. Ensure client issues/deviations are resolved and documented in a timely manner.
• Communicate variances in project budgets, plans and schedules with clients, Business Development and Management. Negotiate necessary changes with clients.
• Assist Business Development to evaluate new business opportunities along with coordinating/developing quotes to close deals.
• Support contract development for product development and manufacturing projects.
• Coach and mentor Product Development Staff, providing feedback to managers and supervisors as needed.
  
  

Qualifications

• Bachelor of Science engineering degree, BSME or BSBME (or related discipline) and experience in the medical device field.
• 6 - 10 years’ experience in a program manager position for a manufacturing company in medical device industry.
• Demonstrated experience leading large complex programs with external and internal customers.
• Technical product development experience, e.g. design, process, or quality engineering.
• Working knowledge of MDR, FDA, and CE design controls
• Strong technical writing ability.
• Leadership ability and organizational skills.
• Strong team oriented professional with good interpersonal skills who is hands-on with a high energy approach to work.
• Proficiency in the use of PC and programs, particularly Project, Excel, Word, PowerPoint.
• Ability to communicate ideas and information clearly, effectively, and frequently (oral and written) both to senior management, customers and associates.
• Execute tasks in a timely manner without direct supervision.
• Thorough understanding and working knowledge of ISO13485.
• Ability to prioritize tasks.
• Applies decision making & analysis tools to align stakeholders, document rationale and achieve optimum outcomes.
• Embedded utilization of Lean tools as necessary for new programs and continuous improvement.
  
  

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.