Description
Job Purpose:Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation.
Ensures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing associate is detail-oriented with strong understanding of automated systems and process controls. Individual will maintain training to the required level and support other functions on site.
Main Responsibilities:
- Actively participates in training activities, managing their individual training plan. Trains other associates as required.
- Executes validation protocols
- Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation
- Perform troubleshooting/investigation of equipment and process issues
- Capable of leading shift when supervisor is absent, and actively leads or participates in shift exchanges. Coordinates activities and daily schedules with cross-functional areas.
- Revises documents as instructed, Capable of equipment and/or process changes
Qualifications
- Solid understanding of the requirements within correct and timely documentation within a cGMP environment.
- Industry or process operator or technical craftsman.
- Must be trained and skilled in all operational and regulatory procedures of manufacturing department
- Relevant education from chemical industry, food industry, pharmaceutical or biotech industry.
- The employee should occasionally be able to make routine decisions based on gained experience.
- Must be able to follow and comply with procedures and protocols.
Michael Bailey International is acting as an Employment Agency in relation to this vacancy.