Quality Assurance Specialist

Grand River Aseptic Manufacturing Located in: Grand Rapids,  Michigan, Midwest
(Private and Secure - Guaranteed!)

Grand River Aseptic Manufacturing Biotechnology Jobs Pharmaceutical Careers
 

JOB DESCRIPTION

CRITICAL REQUIREMENTS

  • Support the quality systems as they relate to the manufacturing and testing of cGMP drug products. Provide quality oversight for terminal sterilization, visual inspection, labeling and packaging Operations of parenteral drugs. Perform the quality release of incoming materials. Review documentation and quality records. Review and approve quality investigations.

COMPANY INFORMATION

Today, the market for parenteral manufacturing services is growing rapidly primarily due to the number of new biologics in development. These innovative products require a partner that understands the complexities of these therapeutics and has the experience, facilities and flawless quality record to meet your timelines. Grand River Aseptic Manufacturing was founded in 2010 as a joint venture between the Van Andel Institute and Grand Valley State University. Our company supports the life sciences industry’s growing need for high-quality, outsourced sterile parenteral manufacturing. We are privately held, with more than 100 employees in two locations near downtown Grand Rapids, Michigan. With nearly 40,000 square feet of sophisticated cGMP space, GRAM meets a full range of fill/finish needs, from early clinical fills through commercialization. All our equipment and processes are fully qualified and validated to ensure cGMP compliance.

JOB INFORMATION

Seniority Level:
Experienced - Not Management
Function:
  Quality
Preferred Industry Background:
  Pharmaceuticals,  Biotechnology
Managing a team of:
N/A
Required Travel:
Not at all

Base Salary:
Confidential
Bonus:
Benefits:
Competitive Salary Health, Dental, Vision Life Short and Long Term Disability 401(k) with match
Other Compensation: