Manufacturing Operator II – Evening Shift
Westport, County Mayo, Ireland · Full Time
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- Experience
- 2+ yrs
- Salary
- —
- Openings
- 1
- Posted
- il y a 6 jours
- Work mode
- In office
- Education
- Leaving Certificate or equivalent
- Resume
- Required to apply
Where you'll work
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Job description
About the Role
Join a world-class team that is passionate about bringing innovative pharmaceutical solutions to market. As a Manufacturing Operator II working the evening shift at AbbVie in Westport, you will play a crucial part in the assembly, inspection, and packaging of pharmaceutical products. Your role will focus on maintaining quality standards while adhering to regulatory and safety requirements in a dynamic production environment.
Key Responsibilities
- Assemble, inspect, and complete manual configurations of product and components to meet Good Manufacturing Practice (GMP) standards.
- Operate semi-automatic production equipment for manufacturing and product finishing.
- Carry out and record quality checks during manufacturing to verify compliance with batch record specifications.
- Transfer materials to and from production lines to support efficiency and correct workflow.
- Follow required safety protocols and utilize appropriate personal protective equipment (PPE).
- Contribute to the maintenance and effectiveness of the quality assurance system.
- Execute manual finishing on pharmaceuticals using both semi-automated and automated machinery.
- Assist with basic activities related to production line changeovers.
- Verify components and testing tools for accurate labeling and packaging of pharmaceuticals.
- Support the setup and closing stages of production orders, including managing end-of-batch clearances.
- Review, audit, and ensure complete and accurate completion of production documentation and data entry.
Qualifications and Requirements
- Completion of Leaving Certificate or equivalent educational qualification.
- A minimum of 2 years' professional experience, ideally within pharmaceutical production.
- Understanding of regulations and standards relevant to pharmaceutical products (such as CFR 210/211, cGMP).
- Prior hands-on experience working in an environment compliant with cGMP is highly desirable.
Additional Information
- Evening shift schedule: Monday to Thursday, 16:00–23:30; Friday, 12:00–18:00.
- This is an initial 6-month contract position.
- AbbVie upholds equal opportunity and is dedicated to integrity, innovation, community involvement, and supporting a diverse workplace.