Quality Control Associate

Payrate: $22.00 – $24.00/hr.

Under general supervision, this position performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good Manufacturing Practices (cGMP), safety guidelines, and regulatory requirements while supporting analytical testing, documentation, and laboratory operations.

• Perform routine laboratory procedures and analytical testing in a regulated QC environment
• Document, calculate, compile, interpret, and enter laboratory data accurately and in a timely manner
• Operate, maintain, and troubleshoot laboratory instruments and specialized equipment as required.
• Maintain laboratory reagents and maintain an inspection ready area
• Maintain complete and compliant laboratory documentation, including logbooks, worksheets, and electronic records
• Follow all applicable safety guidelines, cGMPs, and CFR requirements
• Maintain training records and comply with written procedures and laboratory systems
• Support controlled document updates and change implementation activities
• Identify and escalation compliance, safety, or data integrity issues as appropriate
• May recommend and implement improvements related to routine job functions

• The ideal candidate is a motivated, reliable individual who is eager to grow in a regulated Quality Control laboratory environment. This role is well-suited for:
• Recent graduates or early-career professionals with a Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related scientific field
• Candidates with hands-on QC GMP laboratory experience, even if a degree is not held
• Individuals who are highly trainable and enthusiastic about learning analytical testing techniques
• Team-oriented professionals with strong time management, reliability, and organizational skills
• Candidates comfortable working with basic computer systems and laboratory documentation
• Familiarity with GMP principles is preferred but not required

• Ability to follow regulatory requirements, written procedures, and safety guidelines
• Ability to review and evaluate data and documentation in accordance with company and regulatory standards
• Strong organizational skills with the ability to manage multiple priorities and meet deadlines
• Excellent attention to detail
• Strong written and verbal communication skills
• Flexibility and adaptability in a fast-paced, regulated environment
• Understanding of when and how to appropriately escalate issues
• Ability to identify, recommend, and implement improvements related to routine job functions
• Commitment to continuous learning and compliance with cGMP and safety requirements

• cGMP Compliance & Documentation
• Laboratory Execution & Analytical Skills
• Reliability, Organization & Time Management

The typical base pay for this role across the U.S. is: $22.00 – $24.00/hr final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.