Temp QA Compliance Associate I — 1st Shift, On-Site

Tolmar-7; Fort Collins (CO); On-site; USD 52,000 - 66,000; Full time

Job summary

Tolmar is seeking a Temporary Compliance Associate I for the first shift (Mon-Fri 6:00am-2:30pm) on-site in Fort Collins, CO. The role focuses on QA review of batch records to support product release in line with cGMPs and FDA guidelines.

The assignment runs through March 2027, offering hands-on exposure to regulatory compliance processes, documentation control, and cross‑functional collaboration to ensure timely ship schedules.

Qualifications

• Knowledge of cGMPs and regulatory requirements.
• Organized with strong attention to detail.
• Strong written and oral communication.
• Proficient with MS Word, Excel and Access.
• Ability to work independently across departments.

Responsibilities

• Perform batch record compilation, review and maintenance.
• Review batch records for compliance and accuracy.
• Enter data into databases and spreadsheets to support production schedules.
• Investigate deviations and document findings for QA review.
• Coordinate with departments to obtain records and correct batch errors.
• Prepare final batch records for QA release and scanning.

Skills

Batch records review

cGMP knowledge

Attention to detail

MS Word/Excel

Independent work

Education

High School diploma

Associates degree in technical subject

Job description

Tolmar is seeking a Temporary Compliance Associate I for the first shift (Mon-Fri 6:00am-2:30pm) on-site in Fort Collins, CO. The role focuses on QA review of batch records to support product release in line with cGMPs and FDA guidelines.

The assignment runs through March 2027, offering hands-on exposure to regulatory compliance processes, documentation control, and cross‑functional collaboration to ensure timely ship schedules.