The Production Technician I executes manufacturing processes in formulation, encapsulation, primary and secondary packaging with oversight by Supervision. Sets up equipment for routine processes. Identify and resolve performance related equipment issues in a timely and efficient manner while adhering to GMP guidelines and procedures to meet or exceed target OEE. Execute assigned jobs and maintains operating conditions within the desired range. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout the operations and assists in the implementation of changes both in physical operations and written documents. Displays AbbVie behaviors.
Shifts available:
1st Shift - Days (Sun - Tues every other Wed)
2nd Shift - Nights (Sun - Tues every other Wed) - $1/hr Shift Differential
3rd Shift - Days (Thurs - Sat every other Wed)
4th Shift - Nights (Thurs - Sat every other Wed) - $1/hr Shift Differential
Responsibilities:
- Proficient in Team Member responsibilities or equivalent. Knowledgeable of basic jobs in assigned area of responsibility and Good Manufacturing Practice (GMP) policies. Demonstrates compliance to local and industry quality and safety standards.
- Work directly on the line while executing scheduling priorities, daily assignment, and production expectations for the day. Ability to proficiently operate multiple unit operations across the business. Monitor manufacturing process and communicate any issues that arise with appropriate resources.
- Directly responsible for setting up, running, blowing, cleaning, and clearing equipment according to the BOP/Master batch record.
- Minor troubleshooting on equipment and process related issues and performs repairs. Perform all in process quality checks accurately.
- Trains colleagues on equipment and process for which they are a qualified trainer.
- Demonstrates AbbVie behaviors – good attendance, teamwork, respectful communications, positive attitude.
- Follow all Environmental Health and Safety procedures and guideline policies and participate in safety initiatives.
- Complete batch record steps following ALCOA and GMP processes as needed. Maintain audit ready production area and adhere to all regulations and company policies.