Senior Manager, Service Product Lifecycle; Aesthetic Medical Device Bothell, WA

Job Location:

Bothell, Washington, USA

Job Requisition

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.

• Develop service and reliability requirements in the product requirements documents in collaboration with Product Support and Field Service Teams
• Support identification and development of service tools required for field service and repair center engineers
• Execute service deliverables for end of production and end of service processes to ensure spare parts supply through support life of products

• Collaborate with R&D leadership, product managers, SMEs, and key stakeholders to revise and continuously drive improvements.
• Partner with the market teams and Product Support Engineering to consolidate failure trends and analytics
• Ensure compliance with safety, quality, and regulatory standards throughout product development and sustaining phases.

• Collaborate with R&D and Manufacturing Engineering to resolve issues and improve processes.
• Support repair centers globally with process and tooling support
• Team participates in the design transfer process from R&D and Manufacturing Engineering to Service functions.
• Work with Service Business Analyst to ensure price books in Service Max are up to date

• Oversee technical documentation for products, including design changes, specifications, assembly instructions, travelers, and service manuals.
• Create and manage service process documents to support product release, product revisions and regulatory updates.
• Maintain end item BOM structures and production routes.
• Lead team to execute master data creation for spare parts release for new products and market expansions
• Maintain global parts cost and pricing data

• Lead field and lab testing to verify and validate product modifications and improvements.
• Develop and execute test plans to evaluate product updates for performance and compliance
• Create process and equipment verification and validation plans and reports.

• Bachelor's degree in Mechanical Engineering, Bio Medical Engineering, Electrical Engineering, or related field.

• 10 Year experience in an engineering management role, with a focus on product support, sustaining engineering, manufacturing engineering, preferably in a medical device capital equipment manufacturing environment or another regulated environment.

• Strong understanding of engineering principles, including design, manufacturing, and product lifecycle.
• Knowledge of lean manufacturing principles and tools such as PFMEA, SPC, and DOE.
• Experience with CAD tools, product testing, and analysis.
• Excellent problem-solving and troubleshooting skills.
• Familiarity with industry standards and regulations related to product safety and quality, including FDA Quality System Regulation (QSR) and ISO 9001.

• Strong PC skills required – Word, Excel, PowerPoint, etc.
• Knowledge of product lifecycle management (PLM) tools and processes.
• Familiarity with statistical analysis and reliability testing.

• Individual must have excellent verbal and written communication skills and a demonstrated ability to communicate clearly and professionally.
• The ideal candidate will have the ability to clearly and professionally read, analyze, and interpret engineering specifications, professional journals, technical procedures, and governmental regulations.

While performing the duties of this job, the employee may be required to perform lifting tasks of up to 70 pounds for short durations. Duties of this job may involve standing and/or walking for extended periods of time. Duties also involve daily keyboard data entry. Specific vision abilities required by this job include close vision.