Process Technician

MedPharm•Durham, NC

19h

About The Position

The Manufacturing Operator is responsible for executing a wide range of operations in a cGMP-compliant biopharmaceutical manufacturing environment. This role involves operating, maintaining, and troubleshooting production equipment, performing and documenting complex and critical processes, and supporting equipment validation activities. The operator ensures compliance with standard operating procedures, safety regulations, and documentation standards while contributing to continuous improvement initiatives. Ideal candidates will have an A.A.S. in scientific discipline or equivalent experience, along with 2-4 years of hands-on manufacturing experience. The role also requires strong communication skills, proficiency with MS Office and electronic systems, and the ability to adapt in a dynamic team environment while meeting strict quality and safety standards.

Requirements

A.A.S. in a scientific discipline, or equivalent experience preferred
2-4 years’ experience in a cGMP biopharmaceutical manufacturing environment required
Previous experience as subject matter expert and training others
Existing knowledge of equipment in a manufacturing/production environment
Must be able to work within and adapt to electronic systems
Able to function, with guidance, in a rapidly changing environment while balancing multiple priorities simultaneously
Must be able to be PAPR and Respirator qualified
Able to work independently and as part of a team
Must be able to read, write and converse in English
Must have a good working knowledge of MS Office (Outlook, Word and Excel)

Responsibilities

Operate manufacturing equipment and instruments.
Complete assigned tasks in a timely manner.
Conduct daily activities in an organized, efficient manner.
Perform simple, routine, complex, and critical operations.
Troubleshoot equipment issues, when necessary.
Ensure process equipment is appropriately maintained for operation.
Perform and document operations in accordance with cGMP’s.
Execute equipment qualification protocols and validation protocols.
Recognize and initiate process deviations.
Support continuous improvement initiatives by identifying areas needing improvement, recommending strategies for improvement, and implementing those strategies once approved.
Communicate effectively, both in written and verbal formats.
Maintain training compliance. Ensure a safe working environment for all staff.