Biotechnology Production Technician

RoShay Services; Cohasset (MN); On-site; USD 52,000 - 76,000; Full time

Job summary

RoShay Services is seeking a Production Technician to support cGMP biopharmaceutical manufacturing in a highly regulated environment in Minnesota. You will operate and monitor production equipment, execute batch steps, and maintain accurate documentation to ensure regulatory compliance.

Collaboration with engineers, scientists, and quality teams is essential to troubleshoot, improve processes, and ensure consistent, reliable production of innovative therapies while maintaining strict safety and

Qualifications

• Strong understanding of cGMP expectations and quality documentation practices.
• Ability to perform equipment operations, sampling, and routine analytical tasks.
• Detail-oriented mindset with a focus on compliance, safety, and contamination control.
• Effective teamwork and communication to support issue resolution and continuous improvement.

Responsibilities

• Operate and monitor production equipment used in cGMP manufacturing.
• Execute batch steps according to standard operating procedures (SOPs).
• Maintain accurate, complete documentation to support regulatory compliance.
• Perform in-process sampling and basic analytical checks as required.
• Follow strict safety, quality, and contamination-control practices.
• Collaborate with engineers, scientists, and quality teams to support troubleshooting and process improvements.
• Contribute to consistent, reliable production of innovative therapies.

Skills

cGMP knowledge

Documentation

Equipment operation

Teamwork

Job description

Production Technician supporting cGMP biopharmaceutical manufacturing in a highly regulated environment.

Key Responsibilities

• Operate and monitor production equipment used in cGMP manufacturing.
• Execute batch steps according to standard operating procedures (SOPs).
• Maintain accurate, complete documentation to support regulatory compliance.
• Perform in-process sampling and basic analytical checks as required.
• Follow strict safety, quality, and contamination-control practices.
• Collaborate with engineers, scientists, and quality teams to support troubleshooting and process improvements.
• Contribute to consistent, reliable production of innovative therapies.

Qualifications & Skills

• Strong understanding of cGMP expectations and quality documentation practices.
• Ability to perform equipment operations, sampling, and routine analytical tasks.
• Detail-oriented mindset with a focus on compliance, safety, and contamination control.
• Effective teamwork and communication to support issue resolution and continuous improvement.