Staff Process Development Engineer
Dexcom, Inc

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 we're 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 we've 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. We've already changed millions of lives and we're 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. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've 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:

We are seeking a highly skilled Staff Process Development Engineer with exceptional project leadership capabilities and technical expertise in equipment, test design, statistics, and process development. As a key member of our Engineering team, you will play a pivotal role in leading, developing, and optimizing manufacturing processes for medical devices, ensuring robustness, efficiency, and compliance with regulatory standards.

Where you come in:

• Lead and manage process development projects from concept through commercialization, adhering to timelines and regulatory constraints.
  
• Design and optimize manufacturing processes for new and existing medical devices, focusing on scalability, efficiency, and quality improvement.
  
• Gather and analyze data using statistics, Measurement Systems Analysis, and Design Of Experiments efforts and their associated analysis tools
  
• Utilize statistical tools and methods to analyze process data, conduct capability studies, and implement process controls.
  
• Collaborate cross-functionally with R&D, Quality Assurance, Regulatory Affairs, and Manufacturing teams to ensure seamless roll out of processes into production.
  
• Provide technical expertise in equipment selection, qualification, and validation, ensuring equipment meets performance and regulatory requirements.
  
• Develop and execute test methods and protocols to validate process performance and product quality.
  
• Plan, design, develop, and execute production cost and/or quality improvement projects including all necessary documentation.
  
• Develop and provide status presentations from the technical team up through executive leadership
  
• Mentor and guide junior engineers, fostering a culture of continuous learning and development within the team.
  
• Develop and execute testing and verification, and documentation activities.
  
• Follow design, quality, and safety guidelines based on GMP, FDA, and ISO guidelines and related Quality and Safety Standards and Practices.
  
• Other duties as assigned
  

What makes you successful:

• Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or related field; Master's degree preferred.
  
• Relevant experience within the medical device industry, with demonstrated proficiency in project leadership.
  
• Proven expertise in equipment design, test method development, statistical analysis, and process development.
  
• Experience in at least 1 of the following areas; plastic component assembly, needles, adhesives, epoxies and packaging (sterile barrier, secondary, tertiary).
  
• Experience with statistics, Measurement Systems Analysis, and Design Of Experiments efforts and their associated analysis tools
  
• Strong understanding of regulatory requirements (FDA, ISO, etc.) and experience in developing processes compliant with these standards.
  
• Excellent problem-solving skills and the ability to apply engineering principles to resolve complex technical challenges.
  
• Effective communicator with the ability to present technical information to diverse audiences and stakeholders.
  
• Experience with CAD software (e.g., SolidWorks) and statistical analysis software (e.g., JMP, Minitab) is highly desirable.
  
• Project management certification (PMP) or Six Sigma certification (e.g., Black Belt) is a plus.
  
• Experience with Databases and queries for data collection, aggregation, and analysis
  

What you'll 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.
  

Experience and Education:

• Typically requires a Bachelor's degree in a technical discipline, and a minimum of 8-12 years related experience or Master's degree and 5-7 years equivalent industry experience or a PhD and 2-4 years of experience.
  

Travel Required:

• 25-50%
  

Flex Workplace: Your primary location will be a home office. You will not have an assigned workstation and will work with your manager to determine office visit needs. You must live within commuting distance of your assigned Dexcom site (typically 75 miles/120km).

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. Dexcom's AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com.

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 talentacquisition@dexcom.com.

View the OFCCP's Pay Transparency Non Discrimination Provision at this link.

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: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true

To 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:
$111,100.00 - $185,100.00

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