Pharma Tech Ops Specialist: cGMP & Process Improvement

ADP, Inc.; Clinton (TN); On-site; USD 65,000 - 90,000; Full time

Job summary

Tjoapack is seeking a Technical Operations Specialist to support cGMP manufacturing, troubleshoot production issues, and ensure reliable support for both commercial and clinical operations. The role oversees CPV activities, maintains process performance, and drives cross-functional alignment.

The specialist collaborates with Technical Services, Operations, Quality, Engineering, and EHS; manages documentation routing; and mentors team members to develop capabilities in a fast-paced pharmaceutical

Qualifications

• Must have at least 2 years of experience in a pharmaceutical cGMP Manufacturing setting.
• Related bachelor's degree preferred.
• At least 1 year of experience in Technical Writing (deviations, SOPs, Batch Records, etc.).
• Demonstrated leadership and training experience.
• Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint) preferred.

Responsibilities

• Support cGMP manufacturing operations using data analysis to identify improvements.
• Troubleshoot manufacturing events and author investigations for timely closure.
• Provide ongoing technical support to manufacturing teams.
• Coordinate cross-functional activities to align docs and processes.
• Train manufacturing staff on procedures and batch records.

Skills

Leadership

Communication

Microsoft Office

Technical Writing

Education

Bachelor's degree

Tools

Microsoft Office Suite

Job description

Tjoapack is seeking a Technical Operations Specialist to support cGMP manufacturing, troubleshoot production issues, and ensure reliable support for both commercial and clinical operations. The role oversees CPV activities, maintains process performance, and drives cross-functional alignment.

The specialist collaborates with Technical Services, Operations, Quality, Engineering, and EHS; manages documentation routing; and mentors team members to develop capabilities in a fast-paced pharmaceutical