Sr. Quality Assurance Engineer Lifecore Biomedical Inc.
THIS JOB HAS EXPIRED In this position, you will ensure that new and existing biotechnology processes and systems are validated to comply with regulatory requirements, industry standards, and company policy. You will perform and lead validation activities, manufacturing investigations and create biotechnology process analysis and trending reports. Responsibilities include: review process data trends to proactively identify potential quality problems, investigate root cause and implement effective corrective action; provide knowledge leadership and technical expertise for biotechnology process validations and investigations; insure that validation plan and protocols are comprehensive, clearly written, and technically sound; create validation studies and reports as tools to verify manufacturing controls and process limits; manage process and equipment change to maintain product quality attributes. Requirements: BS in Life Sciences or Engineering (Chemical Engineering Preferred) with 5-8 years of Quality Assurance or Quality Engineering experience. Certified Quality Engineer or Professional Engineer with a background in biology and/or chemistry production processes preferred.
Hours: 4 1/2 or 5 day work week
Lifecore Biomedical's Employee Benefit Program offers employees flexible, comprehensive options and services, allowing an employee to select benefits that are most appropriate to his or her situation.
Medical and Dental Coverage
Flexible Spending Accounts
Short and Long Term Disability
Generous Paid Time Off
Flex Work Week and Time
Employee Assistance Program
||Chaska, MN |
THIS JOB HAS EXPIRED