×
Register Here to Apply for Jobs or Post Jobs. X

Supplier Quality Engineer

Job in Hackensack, Bergen County, New Jersey, 07601, USA
Listing for: GForce Life Sciences
Full Time position
Listed on 2026-02-14
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Biomedical Engineer
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Consultant, Medical Device, Supplier Quality Engineer Summary

Our client, a growing medical device company, has engaged GForce Life Sciences, to identify a Supplier Quality Engineer to assist with ongoing baseline business.

Duties / Expectations of Role

The Supplier Quality Engineer should be familiar with quality functions, process flows, control plans, build instructions, process verification and validations (IQ/OQ/PQ), and quality inspection.

  • Manager Supplier Change requests and initiate Supplier Change Control Processes
  • Track CRF Responses
  • Validating document testing, process flow and document regulations
  • Work on supplier quality contracts
  • Prepare draft Quality and Technical Agreements for existing and new suppliers
  • Work closely with other HCL team working on ECRO process, used to archive the Supplier Quality contract in SAP system.
  • Manage Change requests impacting supplier quality contracts
  • Assisting with Supplier Selection and Qualitfication
  • Assisting with SCARs, Audits, and Supplier Performance
  • Support the Approved Supplier List maintenance/updates
  • Ensure suppliers are compliant via objective evidence/documentation gathered over the course of the project using Client supplier qualification process such as SPPA/PPAP.
Mandatory Requirements
  • Bachelor of Science in Engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE).
  • 3-7+ years of experience in a Quality Engineering role within Medical Device
  • Experience working in a Supplier Quality or Continuity environment
  • Working understanding of QSR/ISO regulations, design assurance, FMEA, Process Flow, and product testing methods.
  • Experience in process validations: creating, reviewing, and approving protocols and reports, and execution of protocols.
  • Experience with PPAP and Gage R&R
  • Experience to include all components of production and process controls including, IQ, OQ, PQ, PPQ, manufacturing equipment software (CSV), and TMV/MSA.
Term & Start
  • 3+ months contract
  • Start in April
  • Onsite/Hybrid in NJ preferred
  • Benefits included (Medical, Dental, Vision, 401k)
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary