Aseptic GMP Manufacturing Technician

AbbVie; Westport; On-site; EUR 32,000 - 52,000; Full time

Job summary

AbbVie in Westport, Ireland, is seeking a Production Operator to support GMP-driven manufacturing within a busy aseptic/solid dosage environment. You will perform daily tasks, maintain documentation, and contribute to batch release targets.

The role emphasizes CAPA handling, quality adherence, and collaboration with cross-functional teams to ensure timely investigation and closure of issues, while following safety and housekeeping standards.

Qualifications

• Experience working in GMP regulated environments is essential.
• Ability to build strong cross-functional relationships and work in a fast-paced setting.
• Strong adaptability to changing constraints with focus on delivering results.
• High energy, maturity, and ability to work under pressure while prioritising tasks.
• Team player with collaboration skills across departments.
• Knowledge of biologics operations is advantageous.
• Excellent communication skills and sound judgement in decision-making.
• Experience with GTW tools and CAPA/Audit processes is preferred.
• 2–3 years in manufacturing, preferably aseptic/sterile environments.
• Experience in cleanroom environments and related safety practices.

Responsibilities

• Carry out daily tasks as assigned by the Production Manager according to GMP and quality system.
• Active involvement and management of batch related CAPAs from review through RCA, approval, disposition and closure.
• Accurately completing documentation in a timely manner.
• Maintain and monitor Grade A conditions inside isolator; use FMS for data collection and glove testing.
• Adhere to safety, housekeeping and quality standards and escalate discrepancies.
• Competent in surface sanitization and disinfection procedures; proficient in SIP sterilization and autoclave counter-pressure training.
• Deliver KPIs related to Product Flow with emphasis on the 32-day release cycle.
• Follow gowning procedures and appropriate garbing for tasks within the compounding area.
• Support EHS & E standards, procedures, and policies.

Skills

GMP knowledge

Cross-functional collaboration

Adaptability

Drive and energy

Team player

Excellent communication

Time management

Problem solving

Education

Third Level qualification in science or engineering

Tools

GTW system

Job description

AbbVie in Westport, Ireland, is seeking a Production Operator to support GMP-driven manufacturing within a busy aseptic/solid dosage environment. You will perform daily tasks, maintain documentation, and contribute to batch release targets.

The role emphasizes CAPA handling, quality adherence, and collaboration with cross-functional teams to ensure timely investigation and closure of issues, while following safety and housekeeping standards.