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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

AbbVie helps people around the world live better days and better lives each year. And that takes all of us.

We are now recruiting for a Contamination Control Operator to join the Biologics department in AbbVie Westport, on an initial fixed-term contract basis. The Biologics business unit manufactures sterile products in aseptic areas, microbial control is achieved within these areas through defined cleaning and disinfection techniques. The Contamination Control Operator is responsible for the cleaning of the aseptic cores and support areas, and the sterility suites within the B1 and B2 facility. They are also responsible for ensuring the areas are stocked and maintained as required for allowing production to proceed.

PLEASE NOTE: The role is a 12 hour rotational shift pattern, covering days, nights, weekdays and weekends.

Responsibilities:

• Perform cleanroom cleaning of the Biologics manufacturing areas which includes Core 1, Core 2, Core 3, Core 4, PFS and sterility suites.  This includes performing post batch, routine and triple cleans in accordance with the relevant procedures.
• Ensuring the relevant areas are stocked with cleaning disinfectants/gloves/gowns/goggles and removal of waste from the area.
• Complete autoclave cycles and filter testing in compliance with procedures.
• Understand and follow gowning procedures and protocols as assigned to assure consistent, reliable, and timely performance of contamination control responsibility within the team and to ensure minimal contamination of the clean room through inadequate gowning.
• Accurately complete documentation and logbooks on time, accurately and legibly.
• Report equipment issues to relevant departments
• Attend all the relevant training sessions and ensure training is completed in a timely manner.
• Complete eLMS training in a timely manner within due dates
• Ensure compliance with all EHS, Quality and housekeeping standards notifying management of any discrepancies.
• Participate in GEMBA’s and Process Confirmations to identify further improvement opportunities within the department
• Adhere to all policies and procedures in support of achieving site metrics.

Key requirements in for this role:

• Experience in Pharma/Medical Devices/Food Operations
• Strong communication and documentation skills
• High attention to detail and methodical in approach
• Ability to be a strong team player and work with cross-functional teams
• Outstanding organization, flexibility, and time management skills
• Ability to multitask and adapt in a fast-paced environment.

Note: Closing date for applications is the 30th December 2025.

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

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