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QA/QC Associate

Location : Edison NJ US 08820
Job Type : Temp/Contract to Direct
Reference Code : 20448-AB1
Compensation : open - 25-35/h
Start Date : 08/10/2021
Hours : Full Time
Required Years of Experience : 2
Required Education : BS Science or Engineering
Travel : No
Relocation : No
Job Industry : Medical Devices

Job Description :

  • Contract to direct position for a QA/QC Associate to conduct pre and final reviews of completed quality documents and records for release of raw materials and components for production and finished goods at a medical device manufacturer.

  • Documents include Batch Records and Incoming Inspection Records.

  • Initiate Quality Issues/Events reporting (Nonconformance, Customer Complaints, CAPA) and assist QA/QC Management in the timely investigation, handling, and completion of these Quality Issues/Events.

  • Assist with quality document creation, revision and filing and other Document Control activities Assist in implementing site product and process changes through established change control process.

  • Conduct QC inspections (Incoming, In-Process and Final Product) using mostly visual inspection and some laboratory equipment including pH meter and micro pipette.

  • Verify product labeling and shipment documentation for completeness and accuracy.

  • Provide recommendations of Quality System improvements/changes.

Required Qualifications :

  • Bachelor's degree in Science or Engineering

  • Minimum 2 years experience in quality documentation review.

  • Experience in QC testing and inspecting.

  • Experience in the medical device or pharmaceutical industry.

  • Knowledge of Microsoft Office (Word and Excel).

  • Detail-oriented, analytical and problem-solving skills with the integrity and interpersonal skills to work in a team-oriented.

Contact: Allan Berman

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