Quality Engineer - Katalyst Healthcares & Life Sciences
South Plainfield, NJ 07080
About the Job
Responsibilities:
- The client has deliverables coming up and needs a consultant to help hit specific deadlines.
- This role is a combo device position, the consultant is required to have experience with prefilled syringes, Class II/III devices, and sterilization.
- There are 3 medical device products, one is already on the market, one will be approved, and they will be launching in Q4 and the last they are filing for shortly.
- The consultant is required to act as the primary QA contact for medical device vendors (packaging and manufacturing), DHF remediation, author and approve DHF documentation, assist with maintaining the QA programs, policies, and procedures and ensure 21 CFR part 820, 210-11 and ISO 13485 compliance of commercial material.
- The consultant will also be required to have experience with investigations with packaging/manufacturing, troubleshooting, gap assessment, and risk assessments.
- The ideal candidate will have experience with combo devices, pre-filled syringes, DHF remediation and documentation.
- Experience over Education.
- Combo device, DHF remediation, pre-filled syringes, QA oversight.
Source : Katalyst Healthcares & Life Sciences