Job Information
AbbVie Contamination Control Operator in Westport, Ireland
Company Description
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 Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description
We are currently looking for a Contamination Control Operator for a 6 month position at our site in Westport, Co Mayo.(shift position)
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.
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.
Qualifications
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.
Additional Information
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.