Senior Supplier Quality Engineer - Electronics (PCB, PCBA)
Senior Supplier Quality Engineer - Electronics (PCB, PCBA)
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$ 87000 - 145000
1 Vacancy
Job Description
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:
TheSenior level Supplier Quality Engineer engages suppliers in three fundamental means:
Supplier evaluation to drive supplier assessments to determine supplier abilities to meet Dexcom requirements.
Material qualification to drive material assessments to determine conformance to requirements.
Supplier development to improve capabilities of key suppliers and/or materials.
In this particular role we are seeking a Senior Supplier Quality Engineer with deep expertise in electronics (PCBs) manufacturing and assembly.
Where you come in:
Maintain the supplier quality management system according to written policies and procedures. Will provide key input on compliance and continuous improvement of business processes.
Provide quality guidance to other departments.
Perform supplier qualification audits monitor supplier performance provide information for supplier program metrics and periodic reports and assist in management of the supplier corrective action system.
Maintains the Supplier Audit Schedule and ensures compliance with this schedule.
May attend and support internal audits by regulatory and other outside agencies.
Establishes and maintains supplier Quality Agreements where needed and any joint periodic supplier business reviews. Reviews and approves supplier documentation (protocols reports specifications etc.) as defined in the Quality Agreements.
May 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.
Have a working knowledge of techniques like six sigma lean manufacturing sampling plans and statistics.
Provides training and guidance to lower level quality engineers and new hires.
Takes the initiative to improve systems and processes that: increase product safety; increase product consistency and conformance to requirements; improve production efficiency and communication; reduce operating and scrap costs.
Reads writes and understands specifications and inspection criteria.
Reads schematics and mechanical drawings and provides input into revisions as needed.
Works and communicates effectively and professionally in a team environment with minimal supervision.
Applies proficient computer skills in the use of Microsoft Office and database applications (such as Oracle Agile and MiniTab).
Has understanding of Design and Process Failure Mode Effect Analysis (DFMEA) and Process Failure Mode Effect Analysis (PFMEA).
Possess knowledge of the Quality Systems Regulations 21CFR Part 820 and international quality systems and medical device standards (e.g. ISO 13485).
Certified or trained to perform quality audits is highly desired.
Experience with supplier quality systems development is highly desired.
Possesses knowledge of techniques like six sigma Gage R&D studies process capability measurement tools (Cpk) lean manufacturing sampling plans and statistics.
Assesses quality performance issues of assigned suppliers using multiple input data streams from Dexcom and the suppliers process to drive / support supplier development activities.
Performs process evaluation of key processes of assigned suppliers to drive / support supplier development activities.
Works cross-functionally to track and trend supplier improvements.
Conducts failure investigations as needed
Travels as needed within in the U.S. and internationally.
Assumes and performs other duties as assigned.
What makes you successful:
Must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Possess deep expertise and manufacturing experience in Electronics (PCB and PCBA manufacturing)
Knowledge in other areas helpful; injection molding extrusion stamping wire manufacturing etc.
Possess continual improvement background (6 sigma Lean Manufacturing etc.).
Excellent communications and excellent collaboration with expected internal and external interfaces. (Internal examples: Supplier Quality Quality Engineering Manufacturing Regulatory Affairs Receiving Inspection. External examples: Suppliers).
Possess and exercise good business acumen.
Ability to manage work with a positive attitude while working in a fast-paced manufacturing environment.
Ability to manage shifting priorities with minimal difficulties.
Previous medical device experience
Previous supplier quality engineering or quality engineering experience
Education and Experience:
Typically requires a Bachelors degree in a technical discipline and a minimum of 5-8 years related experience or Masters degree and 2-5 years equivalent industry experience or a PHD and 0-2 years experience.
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:
25-50%
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:
$87000.00 - $145000.00Required Experience:
Senior IC
Employment Type
Full-Time
