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:
The incumbent is responsible for performing the duties of a Supplier Quality Engineer II, as stated in this job description. Performs tasks with moderate oversight from the manager and/or designated senior level supplier QEs.
Will assist senior quality engineers in the performance of their duties and will support, evaluate, revise and implement specific aspects of the quality system, as assigned. The incumbent will be systematic, highly organized and articulate, and work well in a team environment. Also to be proficient computer skills in the use of Microsoft Office and database applications (such as Oracle and Agile).
Job tasks require interfacing with external suppliers, internal manufacturing, engineering, regulatory, quality, materials, operations personnel and senior management. Will provide guidance and training to technical and administrative personnel, incoming new hires, as assigned.
A positive attitude is important while working in a fast-paced manufacturing environment and dealing with shifting priorities.
Where you come in:
You will maintain the supplier quality management system according to written policies and procedures. Will provide input on compliance and continuous improvement of business processes.
You will provide?quality guidance to other departments as required.?
You will participant to the Supplier Review Committee (SRC) meetings and ensures ongoing supplier program transparency and open communication between cross-functional departments.
You will perform global supplier qualification audits,?monitor?supplier performance,?provide?supplier program metrics and periodic reports, manage the supplier corrective action system.?
You will maintain the Supplier Audit Schedule and monitors compliance with this schedule, on an ongoing basis.
You will serve as the supplier quality representative during internal audits and for designated suppliers, as necessary.??
You will ensure Quality Agreements are?established and that any joint periodic business reviews are conducted. You will review and approve supplier documentation (protocols, reports, specifications, etc.), as defined in the Quality Agreement.??
You will work as a member of the design team, as?required.? Some type of activities may include assisting with defining design inputs; designing components and processes; verifying that design outputs satisfy design inputs.
What makes you successful:
You are required a Bachelor's degree in a technical discipline, and a minimum of 2-5 years related experience or Master's degree and 0-2 years' equivalent experience.
You should have an understanding / experience in stamping, grinding, electro-polishing, moulding, plastics commodities
You must have knowledge of techniques like six sigma, lean manufacturing, sampling plans and statistics.
You must bring the ability to take initiative to develop systems and processes that: improve product safety; increase product consistency and conformance to requirements; improve production efficiency; reduce operating and scrap costs.
You can read, write, understand specifications and inspection criteria.?
Candidate must possess understanding of schematics and mechanical drawings and provides input into revisions as needed.
You should have understanding of Design and Process Failure Mode Effect Analysis (DFMEA) and Process Failure Mode Effect Analysis (PFMEA).
You have knowledge of the Quality Systems Regulations 21CFR Part 820 and international quality systems and medical device standards (e.g. ISO 9001 / ISO
Previous training and/or certification to perform quality audits is highly desired.
You must support the training and guidance to lower-level quality engineers and new hires
You can work and communicate effectively and professionally in a team environment with minimal supervision.
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.
Travel Required:
15-25% - Ability to travel to the U.S. and internationally.
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 unsolicitedresumes/applications.