Job Description

Job Description The Manufacturing Associate I performs and documents cGMP activities to support upstream or downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed.

Lifting to 40 lbs., unassisted may be required at times.

Frequent standing and walking is required, as this role requires presence on the manufacturing floor.

Shift work and weekend work is required.

Key Responsibilities include but are not limited to:

• Performs Processing Steps and/or Manufacturing Support activities, monitoring process against the batch record.

• Documents/Records cGMP data and information for processing steps and/or equipment activities, following standard operating procedures. Key documentation includes batch records and equipment logbooks.

• Understa...