Senior Product Engineer
3 days ago
Solventum is a leading company in the healthcare industry, dedicated to creating innovative solutions that improve lives. We are committed to maintaining the highest standards of integrity and professionalism in our recruitment process.
Job DescriptionWe are seeking a highly skilled Senior Product Engineer to join our team. As a Senior Product Engineer, you will be responsible for maintaining the design for a specific set of commercialized drug products under Solventum's Medical Surgical business.
Key Responsibilities- Maintain the design for a specific set of commercialized drug products under Solventum's Medical Surgical business.
- Lead, execute, and support projects that positively impact quality, performance, service, and cost for assigned product portfolios.
- Collaborate with cross-functional global teams composed of members from manufacturing, regulatory, application engineering, business, clinical, and multiple other functions to drive results.
- Leverage Product and Process Understanding (PPU) initiatives to identify product improvements, then execute change control tasks to implement these changes.
- Collaborate with manufacturing sites and suppliers to address non-conformances, maintain supply continuity, and enhance the customer experience.
- Integrate new products into sustained operations by consulting with New Project Introduction (NPI) teams during Scale Up through design ownership transfer.
- Bachelor's degree or higher in a science or engineering discipline (completed and verified prior to start) from an accredited institution AND (3) years of experience developing, supporting, and/or maintaining commercialized products in a private, public, government, or military environment.
- OR High School Diploma/GED (completed and verified prior to start) AND (7) years of experience developing, supporting, and/or maintaining commercialized products in a private, public, government, or military environment.
- Strong background designing and/or maintaining commercialized drug products under ISO 13485:2016 and FDA 21 CFR part 820 compliance.
- Elevated project management certifications or experiences, including PMP, Scrum, Agile, etc.
- Proven examples of successfully collaborating with laboratory, quality, regulatory, and manufacturing functions on past projects.
- Statistical knowledge and practice of using data to drive product improvements [e.g., Design of Experiments (DOE), sampling, Statistical Process Control (SPC), Product and Process Understanding (PPU), Lean Six Sigma, etc.].
- Strong communication skills (written, oral, and presentation) and Microsoft systems proficiency.
- Competitive compensation package, including base pay and variable incentive pay, if eligible.
- A range of benefits, including Medical, Dental, and Vision, Health Savings Accounts, Health Care and Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and Retirement Benefits.
- Opportunities for professional growth and development.
Please submit your application, including your education and work history, either by uploading a resume or entering the information into the application fields directly. We are an equal opportunity employer and welcome applications from diverse candidates.
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