Pharma Process & Technical Operations Specialist

Tjoapack; Michigan; On-site; USD 90,000 - 120,000; Full time

Job summary

Tjoapack in Clinton, TN is seeking a Technical Operations Specialist to oversee cGMP manufacturing, troubleshoot issues, and support CPV activities across multiple teams. You will help maintain process performance and product quality through data analysis and cross‑functional collaboration.

Responsibilities include document routing, change controls, batch record reviews, and staff training. A minimum of 2 years in pharma cGMP and a related bachelor’s degree is required; MS Office proficiency is

Qualifications

• At least two years of experience in a Pharmaceutical cGMP setting.
• Experience with CPV activities and batch record review.
• Ability to work cross-functionally with Quality, Engineering, and Operations.
• Proficiency with Microsoft Office.

Responsibilities

• Oversee cGMP manufacturing to ensure robust, compliant operations.
• Troubleshoot production issues and author investigations to closure.
• Coordinate CPV activities and monitor process performance.

Skills

Cross-functional leadership

Troubleshooting

Process data analysis

Documentation

Team training

Education

Bachelor's degree in related field

Tools

MS Office

Job description

Tjoapack in Clinton, TN is seeking a Technical Operations Specialist to oversee cGMP manufacturing, troubleshoot issues, and support CPV activities across multiple teams. You will help maintain process performance and product quality through data analysis and cross‑functional collaboration.

Responsibilities include document routing, change controls, batch record reviews, and staff training. A minimum of 2 years in pharma cGMP and a related bachelor’s degree is required; MS Office proficiency is