Production Technician/ Operator I (Night Shift)

About AbbVie

Qualifications

• High school diploma or GED required, technical certificate or degree preferred. Previous general manufacturing experience required, preferably 2-3 years cGMP manufacturing (i.e. food, chemical, petrochemical, consumer products)
• Strong technical aptitude. The ability to troubleshoot and communicate issues to the appropriate operations engineer and mechanical teams.
• Basic computer skills and ability to learn new programs and applications required.
• A demonstrated understanding of the importance of maintaining the highest level of quality and ensuring compliance to site level policies and procedures.
• Demonstrated understanding of HMI controls, vision inspection systems, and product serialization systems.
• Ability to train fellow technicians preferred.
• Understanding and experience with systems such as POMs, SAP, and MAXIMO.
• Requires standing up to 8-12hs per day and lifting up to 25 pounds.

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.