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 GMP QA Documentation Specialist

Details
Country: USA
Location: CO Westminster
Total applied: 20

Career Level: Experienced (Non-Manager)
Salary: From 15.00 to 22.00 USD per hour

GMP QA Documentation Specialist

This is a great foot-in-the door opportunity to join a stable biotech company, located NW of Denver. We have a 6-month temporary position, working in QA - Document Control.

Daily Responsibilities include:
1. Document Control
2. Material Inspection
3. Perform internal audits
4. Technical writing (as needed)

Requirements for this position include:
BS in Chemistry, Biochemistry or related field
GMP experience
2-4 years of laboratory experience
Must also be comfortable handling hazardous chemicals and wearing PPE.

Project management and time management skills are essential. This position is Monday-Friday, 8 a.m.-5 p.m., with occasional overtime.

If interested in this position, please apply online or call 303-427-4140.

Kelly Scientific Resources is recognized as the world leader in the scientific staffing industry. Our experiences staff identifies and employs top-notch talent. Our unique training provides outstanding long-term career development opportunities.Kelly Services is an Equal Opportunity EmployerContact?Information?:.Sheridan Park 2
Westminster?CO?80031

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