Technical Sourcing Engineer III - OEM

About the role

The Staff Technical Sourcing Engineer (TSE) plays a pivotal role in our Global Value Assurance Organization. You will determine strategies for cost savings, cost avoidance, and revenue generation, while strictly ensuring risk mitigation and supplier quality. Your contributions will enable us to continue delivering world-class solutions that make the world healthier, cleaner, and safer.

Responsibilities

• Collaborate with R&D, product development, quality, procurement, and strategic sourcing to align the global sourcing strategy.
• Successfully conduct cost reduction and manufacturing scale-up initiatives at OEM suppliers.
• Resolve supplier quality issues to maintain our detailed production standards.
• Focus primarily on OEM Instruments and Equipment.
• Travel up to 20% globally to support and coordinate supplier activities and projects.

Requirements

• Education: Bachelor’s or Master’s in Mechanical Engineering, Mechatronics, Electrical Engineering, or Physics. Equivalent field are also acceptable.
• Experience: BS with 5+ years experience, or, MS with 3+ years’ experience: hands on product design, product development, and manufacturing experience.
• Expertise: In Mechanical assembly design or cast, machined, and sheet-metal part design.
• Skills: Strong project management skills with a consistent track record. Experience working directly with OEM suppliers and contract manufacturers. Experience leading vendors, contract manufacturers, and design firms. Proficiency in value engineering, process development, should-cost modeling, and DFA/DFM/DFx methodologies. Demonstrated ability to manage electromechanical suppliers and contract manufacturers. Knowledgeable in regulatory standards such as FDA, NSF, CSA, UL, ISO 13485 in the medical products industry. Skilled in CAD Design software such as SolidWorks, Pro/e, or equivalent. Understanding of phase gate development processes across diverse teams is helpful. Medical devices experience is helpful.

Qualifications

• Knowledge: Expertise in building should-cost models for sourced materials.
• Abilities: Ability to work independently under ambiguous demands within a global organization. Demonstrated technical writing skills for producing detailed reports and documents.

Skills

• Expertise in value engineering, process development, should-cost modeling, and DFA/DFM/DFx methodologies.
• Understanding of regulatory standards such as FDA, NSF, CSA, UL, ISO 13485 in the medical products industry.
• Proficiency in CAD Design software such as SolidWorks, Pro/e, or equivalent.
• Understanding of phase gate development processes across diverse teams is helpful.
• Medical devices experience is helpful.

Benefits

Not specified.

Pay

Not specified.

Schedule

Standard (Mon-Fri).

Environmental Conditions

Office.