Senior Process Engineer

Location: California
** Our Ambition & Vision
** Our vision is to create an
** intelligent, connected, and reliable supply chain**—transparent, data-driven, and always improving. By combining
** collaboration, innovation, and operational excellence**, we’re building a network that’s
** agile, sustainable, and ready for the future**.
** Let’s talk about Responsibilities
**** Process & Equipment Development
*** Design, develop, and optimize motor manufacturing processes and tooling to meet quality, performance, and cost targets.
* Lead
** process validation** (IQ, OQ, PQ) to ensure compliance with
** FDA QSR**,
** ISO 13485**, and
** GMP
* * requirements.
* Apply
** Design for Manufacture (DFM)
** and
** Design for Assembly (DFA)
** principles to ensure scalable, robust production.
* Develop and enhance automation, test systems, and fixtures using
** Solid Works
* * or equivalent tools.
** Continuous Improvement
*** Analyze production data using
** Lean, Six Sigma**, and
** DOE
* * techniques to identify improvement opportunities.
* Implement corrective and preventive actions (CAPA) to improve yield, reduce waste, and enhance reliability.

Our ambition is to build a
** next-generation, best-in-class supply chain
** that gives Res Med a true
** competitive advantage
** through outstanding
** value, quality, and availability**. We strive to be a
** trusted partner
** that connects technology, people, and purpose to deliver exceptional outcomes for our customers and patients around the world.
** About the Role
** As a
** Senior Process Engineer** ****–
** Motors Engineering**, you’ll play a key role in shaping how our products are made. You’ll design, refine, and optimize motor manufacturing processes that deliver exceptional
** safety, quality, and efficiency**. You’ll work across engineering, production, and quality teams to ensure smooth transitions from design to high-volume manufacturing—helping Res Med continue to deliver life-changing technology with precision and purpose.

Your success will be measured through your ability to
** build reliable, compliant, and efficient manufacturing processes
** that drive measurable impact:
Minimum two improvement projects per year delivering measurable cost, quality, or efficiency benefits.
* Zero recordable safety incidents or audit findings related to manufacturing processes.
* 100% compliance with GMP, ISO 13485, and EHS audit standards.
** Collaboration & Growth
*** Positive stakeholder feedback across Engineering, Quality, and Operations.
* Demonstrated mentorship and technical leadership within the team.
** Let’s talk about Qualifications and Experience**
* *
* Education:

** Bachelor’s degree in Mechanical, Mechatronics, Manufacturing, or Industrial Engineering.
* *
* Experience:

** 5–8 years in manufacturing or process engineering, ideally within medical devices or precision manufacturing.
* *
* Skills:

**  + Expertise in process validation, DFM/DFA, and continuous improvement.  + Proficiency in
** Solid Works**,
** Minitab**, and DOE methodology.  + Working knowledge of
** GMP**,
** ISO 13485**, and regulatory compliance.  + Experience in applying functional knowledge and existing methodologies to solve complex problems or execute specialized projects. (moved from preferred)  + Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results. (moved from preferred)  + Strong experience in Design of Experiments (DOE) for process optimization and validation. (edit of original line)
* ** Preferred**  + Hands-on experience with PLC programming and automation systems for process control (re-worded)  + Demonstrates aptitude in developing new methodologies and procedures for New Product Introduction (NPI) tasks.  +

Experience with coordinating with and managed external vendors for equipment design/delivery.
* ** Mindset:
** Hands-on, data-driven, and collaborative — passionate about building processes that improve lives.
** Why Join Us
** At Res Med, we believe in **“Do it Best, Do it Together.”
** You’ll join a forward-thinking team driving innovation in medical device manufacturing — where engineering precision meets purpose. Together, we’re creating smarter, safer, and more…