R&D Senior Systems & Mechanical Engineering Manager
Mentor, OH, US, 44060
At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Position Summary
The R&D Senior Systems & Mechanical Engineering Manager for the Reprocessing business leads an R&D team focused on advanced medical device development. This role serves as a technical authority, shaping the technology vision and integrating innovative solutions into product designs.
Note: “R&D Senior Systems & Mechanical Engineering Manager”, Hybrid role requiring 3 days onsite at STERIS Headquarters in Mentor, Ohio.”
What You'll Do As A R&D Senior Systems & Mechanical Engineering Manager
- Lead an R&D team in Systems and Mechanical Engineering for advanced medical device development, serving as a technical authority and guiding technology vision.
- Integrate cutting-edge solutions into products, oversee patent and technology strategy, and ensure efficient project progress.
- Facilitate clear communication among project teams and stakeholders, standardize execution frameworks, and foster cross-functional collaboration.
- Evaluate strategies, resources, and alternatives to achieve objectives, balancing immediate needs with long-term goals.
- Provide market and competitive insights to inform strategic direction; mentor staff in technical and regulatory matters to enhance value.
- Drive continuous improvement initiatives for R&D, including training, development, and organizational assessment.
- Oversee stakeholder requirements translation, manage adherence to safety, clinical, serviceability, manufacturability, reliability, and quality standards.
- Direct Systems and Mechanical Engineering activities throughout project lifecycles, participating in feasibility studies, design reviews, and risk management.
- Collaborate with Project Management on task definition and scheduling; contribute to system architecture and technology roadmaps.
- Implement best practices, technical assessments, and LEAN initiatives, ensuring regulatory compliance and user satisfaction.
- Guide system integration, verification, validation, and problem resolution; define and oversee testing protocols across products.
- Manage product design, development, and support, including people management, budgeting, and vendor relationships.
- Ensure workplace safety, security training, and compliance with quality systems, FDA regulations, and company policies.
- Administer budgets, monitor risks and dependencies, promote high performance, and optimize processes within the department.
The Experience, Skills, and Abilities Needed.
Required:
- Bachelor’s degree in Mechanical Engineering required
- Minimum of 15 years of related experience required
- Minimum 10 years of experience applying systems engineering in R&D for medical devices
- Minimum 10 years of experience supporting NPD/LCM programs
- Minimum 5 years of experience managing / directing an R&D Team
- 5+ years’ experience developing FDA regulated medical devices
- Ability to work in a highly regulatory environment
- Strong analytical skills
- Exposure to project / program management skills required
- Must have excellent leadership, interpersonal and influencing skills and have a demonstrated ability to lead global, cross-functional, multi-disciplinary teams. Demonstrated leadership skills including conflict resolution, assertiveness and negotiation skills required.
- Demonstrated proficiency in driving continuous improvement for performance, quality, time and cost; strong planning and organization skills required.
- Demonstrated ability to make sound data driven business decisions; Understand, track, drill down and question activities and issues in all functional area. Strong attention to detail, follow-through skills
Sets the standard for timeliness, work ethic, and personal integrity. - Must have excellent written communication skills – reports, presentations
- Working knowledge with Windchill, CREO, and Microsoft Project
- Exceptional team player
- Travel up to 10% including internationally
- Must have the ability to work in a lab environment & the ability to lift up to 50 pounds.
Preferred:
- Masters in Engineering Discipline, MBA
- Experience in more than one of the following functional areas: Operations, Supply Chain, Quality
- Experience in LEAN Methodologies
- Experience with Finite Element Analysis and simulation tools
What STERIS Offers:
We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future.
Here is a brief overview of what we offer:
- Market Competitive Pay
- Extensive Paid Time Off and (9) added Holidays
- Excellent Healthcare, Dental and Vision Benefits
- Long/Short Term Disability Coverage
- 401(k) with a company match
- Maternity and Paternity Leave
- Additional add-on benefits/discounts for programs such as Pet Insurance
- Tuition Reimbursement and continued education programs
- Excellent opportunities for advancement in a stable long-term career.
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Pay rate for this opportunity is $141,737.50 - $175,087.50. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
Mentor, OH, US, 44060
Nearest Major Market: Cleveland
Nearest Secondary Market: Akron
Job Segment:
R&D Engineer, R&D, Medical Device, Medical Device Engineer, Supply Chain Manager, Engineering, Research, Healthcare, Operations