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Quality Assurance Associate

Job in Covington, Kenton County, Kentucky, 41011, USA
Listing for: ProQuality Network
Full Time position Listed on 2026-11-13
Job specializations:
Salary/Wage Range or Industry Benchmark: 52000 - 70000 USD Yearly USD 52000.00 70000.00 YEAR

Job Description & How to Apply Below

Job Title: Quality Assurance Associate (Biotechnology Industry) –  / 3556776

Location: Kentucky, U.S. (Open to local residents)

Positions Available: 1

Work Arrangement: Onsite

Shift: Monday – Friday | 2:00 PM – 10:30 PM

Position Summary:

Pro Quality Network is seeking a Quality Assurance Associate to support our client in the biotechnology industry. This is a contract-to-hire opportunity designed to assist with quality operations in a regulated GMP environment
. The selected candidate will be responsible for reviewing analytical documentation and ensuring compliance with established regulatory requirements and internal quality systems.

The ideal candidate will demonstrate strong critical thinking, attention to detail, and organizational skills
, along with the ability to make sound decisions based on applicable GMP regulations
. Professional, effective, and proactive communication with peers, management, and cross-functional teams is essential to support quality and compliance across operations.

Key Responsibilities:

  • Review analytical release and stability data to ensure compliance with GMP and internal quality standards.
  • Perform review and approval of controlled documents
    , including protocols, test methods, and specifications.
  • Evaluate analytical documentation such as test methods, protocols, and stability/release data with minimal supervision.
  • Ensure documentation accuracy, completeness, and compliance with regulatory and quality system requirements.
  • Collaborate with cross-functional teams to support quality objectives and maintain regulatory compliance.

Education and Experience:

  • Bachelor’s degree in a scientific discipline
    , preferably Chemistry or Biochemistry
    .
  • Minimum of 3 years of GMP industry experience
    .
  • Relevant experience in analytical laboratories, Quality Control (QC), manufacturing, or Quality Assurance (QA) within regulated environments.

Position Requirements

10+ Years work experience
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