QA Associate I – cGMP Lab & Documentation

Colorado State University; Fort Collins (CO); On-site; USD 50,000 - 65,000; Full time

Benefits offered by this job

Comprehensive benefits package

Work-life balance initiatives

Job summary

A prominent educational institution in Fort Collins is seeking a QA Associate I to assist with laboratory activities related to cGMP biological material for early Phase Clinical trials. Responsibilities include reviewing documentation, ensuring compliance with regulatory requirements, and maintaining quality management systems. The ideal candidate will have a Bachelor's degree and experience in a regulated environment, with a salary range of $50,000 – $65,000. Background checks are part of the employment process.

Qualifications

• Ability to assist in QA documentation and policy updates.
• Willingness to work under BSL-3 conditions.
• Basic knowledge of safety and biosafety practices.

Responsibilities

• Review cGMP documentation for completeness.
• Issue documents needed for operations and projects.
• Participate in the Quality management system.

Skills

Attention to detail

Understanding of cGMP systems

Documentation compliance

Education

Bachelor’s degree in Science

Bachelor’s degree in an unrelated field with 1-2 years of experience

Job description

A prominent educational institution in Fort Collins is seeking a QA Associate I to assist with laboratory activities related to cGMP biological material for early Phase Clinical trials. Responsibilities include reviewing documentation, ensuring compliance with regulatory requirements, and maintaining quality management systems. The ideal candidate will have a Bachelor's degree and experience in a regulated environment, with a salary range of $50,000 – $65,000. Background checks are part of the employment process.