Production Technician l

Allergan; Tempe (AZ); On-site; USD 42,000 - 65,000; Full time

Job summary

AbbVie in Tempe, AZ seeks a Production Technician I to execute manufacturing processes in formulation, encapsulation, and packaging under GMP with supervision.

You will set up equipment, operate multiple unit operations, perform quality checks, and troubleshoot while following ALCOA and safety. The role offers 1st-4th shifts with differential; strong teamwork required.

Applicants should have a high school diploma or GED, 2–3 years in cGMP manufacturing, and ability to train others.

Qualifications

• High school diploma or GED; technical certificate or degree preferred.
• 2–3 years of cGMP manufacturing experience.
• Ability to troubleshoot and communicate issues clearly.
• Understanding of GMP, ALCOA, and safety procedures.

Responsibilities

• Set up, run, blow, clean, and clear equipment per batch records.
• Perform in-process quality checks and minor repairs.
• Monitor production line and communicate issues to appropriate resources.
• Train colleagues on equipment and processes.
• Maintain audit-ready production area and ensure compliance with policies.
• Adhere to safety and quality guidelines throughout operations.

Skills

GMP knowledge

Troubleshooting

Technical aptitude

Teamwork

Training others

Electrical/Mechanical

Education

High school diploma or GED

Technical certificate or degree

Tools

SAP

MAXIMO

POMs

Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

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.

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.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term incentive programs.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html