Manager - Process Engineering
Job in
San Diego, San Diego County, California, 92189, USA
Listed on 2026-09-25
Listing for:
Dexcom Inc.
Full Time
position Listed on 2026-09-25
Job specializations:
-
Engineering
Quality Engineering, Manufacturing Engineer, Process Engineer
Job Description & How to Apply Below
Meet the team:
Our Manufacturing Process Engineering team is part of the San Diego Innovation Center of Excellence, driving the development, transfer, and scale-up of manufacturing processes and equipment for new products. In the Pilot Manufacturing environment, we focus on bridging R&D product concepts and full-scale production—developing robust processes, characterizing performance, and ensuring compliance with Design Control requirements.
Where you come in:As Process Engineering Manager, you will provide technical leadership to a team of engineers and scientists to:
- Lead process development, process characterization, and support pilot manufacturing, ensuring processes are robust, well-defined, and compliant with Design Controls, ISO 13485, FDA compliance, and regulatory requirements.
- Define and oversee Design of Experiments (DOE) to characterize processes, validate changes, and optimize performance using statistical analysis tools (Gauge R&R, Cp/Cpk, SPC).
- Manage the documentation and execution of experimental requests on pilot manufacturing lines, ensuring proper process controls, traceability, and alignment with product design requirements and Design Development Plans.
- Monitor pilot line performance, identify trends, and drive improvements through data-driven decision-making and continuous improvement strategies.
- Interpret build data and process metrics to assess variability, identify root causes, and implement corrective actions using advanced statistical methods.
- Oversee the transfer and sustaining of processes, test methods, and equipment from development into pilot operations, ensuring product functionality and cost-effectiveness.
- Collaborate cross-functionally with R&D, Quality, and Operations to align on process specifications, risk management (PFMEA), and validation strategies (IQ, OQ, PQ).
- Provide hands‑on technical guidance for manufacturing workflows, specialized equipment, analytical testing tools, and pilot-scale facilities within a regulated environment.
- Champion New Product Introduction (NPI) roadmaps and strategies, driving innovation and operational excellence.
- Select, develop, and mentor engineering talent, fostering a culture of technical rigor and collaboration.
- Ensure compliance with safety, environmental, and quality standards across all pilot manufacturing activities, supporting regulatory submissions as needed.
- Proven experience managing engineers and scientists, with cross functional disciplines, focused on manufacturing processes, product release testing, and investigations.
- Knowledge of DMAIC process, structure problem solving, lean manufacturing and project management with proven success of implementation.
- Proven engineering experience supporting and managing regulated GMP/GLP operations, preferably in medical device, medical diagnostic, and/or pharmaceutical industries.
- Knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO 13485 Quality management systems).
- Excellent written and oral skills, driving efficient and effective communication cross functionally.
- Proven ability to collaborate and drive results in a matrix organization.
- Recommended to have a STEM degree with proven ability to work hands‑on in a fast‑pasted environment with competing priorities.
- A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
- A full and comprehensive benefits program.
- Growth opportunities on a global scale.
- Access to career development through in-house learning programs and/or qualified tuition reimbursement.
- An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities…
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