Staff Manufacturing Engineer

The Company

Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later having pioneered an industry. And were just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized actionable insights aimed at solving important health challenges. To continue what weve started: Improving human health.

We are driven by thousands of ambitious passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening serving with integrity thinking big and being dependable. Weve already changed millions of lives and were ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. Well get there by constantly reinventing unique biosensing-technology experiences. Though weve come a long way from our small company days our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.

Meet the team:

Join our Manufacturing Engineering team at the San Diego Innovation Center of Excellence to support the development of products and processes and transfer into operations with a primary focus on advancing our applicator technology.

As a Staff Manufacturing Engineer you will be responsible for day-to-day technical support for pilot plant operations and lead process and equipment enhancements.

Where you come in:

• Lead cross-functional development validation and implementation of manufacturing processes to support new product introductions design changes and commercial production readiness.
• Drive process capability quality and yield improvements through the application of statistical tools such as DOE SPC Gauge R&R and structured root cause analysis.
• Own process validation activities including development and execution of IQ/OQ/PQ protocols validation strategies and supporting documentation required for regulatory compliance.
• Provide technical leadership and project management for complex engineering initiatives coordinating stakeholders across R&D Manufacturing Quality Supply Chain and Operations.
• Assess and mitigate process and product risks by contributing to PFMEAs process specifications validation plans CAPAs and change control activities within a regulated quality system
• Mentor engineers and influence engineering strategy by establishing best practices providing technical guidance and leading long-term process and technology improvement roadmaps.

What makes you successful:

• Expertise in pilot-scale or high-volume manufacturing process validation equipment qualification and measurement systems.
• Project Management leadership in areas focusing on design changes process improvements and other plant efficiency efforts in regulated industries preferably in the medical device.
• Expertise in applying statistical tools used to assist in the development and troubleshooting of products and processes.
• Proven ability to work hands-on in a fast-paced environment multitask prioritize projects maintain timelines and communicate updates to management.
• You have demonstrated the ability to work cross-functionally as a team player with strong critical thinking mentoring and coaching skills.

What youll get:

• 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 we serve.

Travel Required:

• 0-5%

Education and Experience:

• Typically requires a Bachelors degree in a technical discipline and a minimum of 8-12 years related experience or Masters degree and 5-7 years equivalent industry experience or a PhD and 2-4 years experience.

Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may at its discretion assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin or protected veteran status and will not be discriminated against on the basis of disability. Dexcoms AAP may be viewed upon request by contacting Talent Acquisition at

If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process please contact Dexcom Talent Acquisition at

Meritain an Aetna Company creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files please click on the URL provided: all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

Salary: