Contamination Control Supervisor

AbbVie

Westport

On-site

EUR 55,000 - 75,000

Full time

14 days+

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Job summary

AbbVie Westport is seeking a proactive Shift Supervisor to lead the Contamination Control team in our aseptic fill-finish operation. The role requires coordinating day and night shifts on a monthly rotation, ensuring cleanroom sanitisation and GMP-compliant practices within the Biological cores.

You will mentor operators, manage KPI-driven workflows, maintain audit-ready documentation, and collaborate with cross-functional teams to support new product introductions and technology transfers at

Qualifications

  • 3rd level qualification in science or engineering discipline.
  • Strong technical knowledge and application of concepts, practices, and procedure.
  • Excellent interpersonal and communication skills for cross-functional work.

Responsibilities

  • Lead and develop the contamination control team.
  • Coordinate contamination control activities respecting production schedules and KPIs.
  • Ensure audit readiness of areas and documentation.
  • Perform cleanroom sanitisation and autoclave-related tasks per GMP.
  • Maintain supplies and report equipment issues.
  • Complete training and ensure compliance with EHS and quality standards.

Skills

Strong technical knowledge
Good interpersonal communication

Education

3rd level qualification in science or engineering related discipline

Job 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.

Job Description

About the Opportunity

AbbVie Westport is the largest operating facility in the AbbVie global network and a recognised centre of excellence for aseptic fill‑finish operations. Our Westport site is a dynamic, fast‑paced environment with a strong pipeline of new product introductions, technology transfers, and development projects spanning both small and large molecule programmes.

We are looking for a talented and driven Shift Supervisor for our Contamination Control team.

The Contamination Control Supervisor at AbbVie Westport is responsible for leading a team of contamination control operators (CCO) responsible for sanitising cleanrooms, support and ancillary areas in the Biological cores at Abbvie Westport. This is a shift‑based role rotating between days and nights on a monthly basis, so ability to work shifts is essential.

Responsibilities
  • Manage, motivate, and develop the contamination control team through effective communication, performance reviews and coaching.
  • Lead and coordinate all contamination control activities on the assigned shift, ensuring activities are prioritised and executed in line with production requirements, schedules and Key Process Indicators (KPIs).
  • Escalate risks and performance issues in a timely manner to the Contamination Control Manager.
  • Ensure assigned areas and CCO associated documentation is audit ready at all times.
  • Perform cleanroom sanitisation 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 and Good Manufacturing Practices.
  • 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 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 in compliance with Good Documentation Practices.
  • Report equipment issues to relevant departments.
  • Attend all the relevant training sessions and ensure training is completed in a timely manner.
  • Ensure eLMS training is completed 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
  • 3rd level qualification in science or engineering related discipline.
  • Strong technical knowledge and application of concepts, practices, and procedure.
  • Good interpersonal and communication skills essential for working across multi‑functional teams.
Additional Information

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 applicants seeking a reasonable accommodation, click here to learn more:

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