Senior Validation Engineer Lifecore Biomedical Inc.
THIS JOB HAS EXPIRED Job Description:
This individual will define, execute, review, approve and summarize equipment, process, facility, and sterilization (EtO, gamma) validation documentation, including investigation into failures. They will use quality engineering concepts to monitor, support, and critically review changes or issues to existing product lines and/or critical processes; review and approve appropriate controlled documentation (ex. validation protocols and reports, product related documents, nonconformances, etc.). They willl insure data is reviewed and trends are investigated in a manner to ensure product quality.
BS in Life Sciences or Engineering with 5-8 years of Validation or Quality Engineering experience. Background in pharmaceutical, biotechnology and/or chemistry production preferred. Certified Quality Engineer or Professional Engineer preferred. Experience in the medical device, drug and/or API equipment and process validation activities. Experience leading sterilization process (EtO, gamma), equipment and process validation activities. Risk assessment (FMEA, FTA, etc.) experience.
Medical and Dental Coverage
Flexible Spending Accounts
Short and Long Term Disability
Generous Paid Time Off
Employee Assistance Program
Hours: 4 1/2 or 5 day work week
||Chaska, MN |
THIS JOB HAS EXPIRED