Chaska Categories:
Senior Quality Assurance Specialist Lifecore Biomedical Inc.
THIS JOB HAS EXPIRED
Job Description:In this position you will provide QA review/approval for batch records, validation documentation and other documentation as required. You will maintain the validation master plan documents ensuring accurate summary of validation documentation supporting each product line and annual review of in-process parameter trending. Lead quality system improvement implementation projects as assigned. Ensure new and existing processes, systems, and methods comply with regulatory requirements, industry standards, and company policy.
Job Requirements:
BA/BS in Life Sciences or Engineering. 5+ years experience in medical device or pharmaceutical industry with 5-8 years of Quality Assurance experience. Preferred Certified Quality Auditor. Technical writing experience and knowledge of basic statistics. Proven ability to provide QA review of batch records, validation documents, and other technical documents. Comprehensive understanding of QSR/ISO/ICH regulations for medical devices and active pharmaceuticals.
Benefits:
Medical and Dental Coverage
Matching 401K
Flexible Spending Accounts
Short and Long Term Disability
Life Insurance
Paid Holidays
Generous Paid Time Off
Employee Assistance Program
Exercise Room
Hours: 4 1/2 or 5 day work week
| Location: | Chaska, MN United States |
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THIS JOB HAS EXPIRED
Lifecore Biomedical Inc.
Investors: Warburg PincusAll Jobs: at Lifecore Biomedical Inc.
| Web Site: | www.lifecore.com |
|---|---|
| Headquarters: | 00000 United States |
| Industry: | Biotechnology |
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