Quality Assurance Specialist

2 weeks ago


Brighton, Michigan, United States Bryllan LLC Full time
Quality Assurance Associate Job Description

Bryllan LLC, a rapidly growing Contract Manufacturing Organization (CMO), is seeking a highly motivated and detail-oriented Quality Assurance Associate to join our team. As a Quality Assurance Associate, you will play a critical role in ensuring the quality and integrity of our pharmaceutical products.

Key Responsibilities:
  • Develop, review, and approve quality-related documents, including batch records, protocols, and reports.
  • Lead quality assurance activities in support of new product and manufacturing operations.
  • Review and approve incoming materials, including active pharmaceutical ingredients, excipients, and packaging materials.
  • Perform quality oversight during manufacturing operations, identifying and implementing process improvements.
  • Develop and implement Standard Operating Procedures (SOPs) related to cGMP quality systems.
Behavioral Expectations:
  • Strong work ethic and ability to accomplish tasks without supervision.
  • Exhibits leadership, both by work and example.
  • Strong organizational skills and ability to focus on multiple projects in a fast-paced environment.
  • Excellent interpersonal skills with the ability to communicate effectively.
Requirements:
  • 5+ years of experience in the pharmaceutical/biotech industry.
  • Demonstrated knowledge and understanding of cGMP and cGMP Quality Systems.
  • 4-year degree in a scientific discipline.
Compensation Package:
  • Salary will be determined by experience, with a range of $58,656 - $65,000.
  • Benefits include paid time off, medical, dental, and vision insurance, and short-term and long-term disability insurance.

Bryllan LLC is an equal opportunity employer and welcomes applications from diverse candidates. All employment offers are contingent upon the successful passage of a pre-employment drug screen and background check, including FDA Debarment verification status.



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