Supplier Quality Engineer
Job in
Hackensack, Bergen County, New Jersey, 07601, USA
Listed on 2026-02-14
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
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 RoleThe 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.
- 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.
- 3+ months contract
- Start in April
- Onsite/Hybrid in NJ preferred
- Benefits included (Medical, Dental, Vision, 401k)
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