Sterile QC Technician — Cleanroom & GMP Focus

Actalent; Saint Paul (MN); On-site; USD 56,000 - 69,000; Full time

Benefits offered by this job

Medical, dental, vision, and life

401K with company match up to 4%

Profit sharing

Job summary

Actalent is seeking a Quality Control Technician to support process and product quality by preparing equipment, samples, and materials for testing in a fast-paced, small-company environment. The role emphasizes environmental monitoring in cleanrooms, review of batch records, and collaboration with third-party labs to ensure sterility and regulatory compliance.

The ideal candidate will have at least 2 years in a regulated industry, strong documentation skills, and experience with sterilization

Qualifications

• Experience in regulated industries such as medical device, pharmaceutical, or food.
• Hands-on environmental monitoring in cleanrooms is required.
• Experience with sterilization processes and sterile environments preferred.
• Familiarity with GMP and SOPs; strong attention to documentation.

Responsibilities

• Perform environmental monitoring of cleanrooms and verify pest control measures.
• Collect and submit samples to labs for analysis and ensure timely results.
• Review batch records and sterilization certificates for readiness of product release.
• Prepare chemical formulations and perform in-process QC tasks.
• Maintain accurate equipment maintenance and QC records.
• Support CAPAs and investigations for non-conformances with data analysis.

Skills

Environmental monitoring

GMP knowledge

SOP adherence

Documentation

CAPA investigations

Data analysis

Batch record review

Quality mindset

Education

Associates or Bachelors in science

Job description

Actalent is seeking a Quality Control Technician to support process and product quality by preparing equipment, samples, and materials for testing in a fast-paced, small-company environment. The role emphasizes environmental monitoring in cleanrooms, review of batch records, and collaboration with third-party labs to ensure sterility and regulatory compliance.

The ideal candidate will have at least 2 years in a regulated industry, strong documentation skills, and experience with sterilization