Aseptic GMP Manufacturing Technician - Weekend Shift

SmartRecruiters, Inc.; Waterford; On-site; EUR 34,000 - 42,000; Full time

Job summary

AbbVie is seeking a Manufacturing Technician for the weekend shift to support GMP-compliant production, CAPA execution, and documentation in a sterile environment. The role requires working in a cleanroom and adhering to safety and quality standards, with cross-functional collaboration across teams.

Strong technical writing skills and the ability to prioritize tasks are essential. The position emphasizes maintaining isolator conditions, using the FMS system for data collection, and following

Qualifications

• 2-3 years working in a manufacturing environment, preferably aseptic/sterile manufacturing.
• Experience working in a cleanroom environment.
• Excellent technical writing skills are required for this role.
• Ability to build strong relationships and work within cross-functional teams.
• Able to work in a fast, dynamic environment, meeting unexpected constraints.

Responsibilities

• Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system.
• Actively manage batch-related CAPAs from review through RCA, approval, batch disposition and corrective actions.
• Accurately completing documentation in a timely and legible manner.
• Maintain and monitor grade A conditions inside isolator; use FMS data collection and glove testing for integrity of RAB units.
• Follow gowning procedures and wear appropriate garbing for tasks within the compounding area.
• Adhere to safety, housekeeping and quality, notifying management of discrepancies.
• Support EHS & standards, procedures, and policies.

Skills

GMP knowledge

Documentation

CAPA handling

Cross-functional collaboration

Regulatory compliance

Adaptability

Education

Bachelor's degree in science or engineering

Third Level qualification in science or engineering

Tools

FMS system

Autoclave

Disinfectants/Biocide protocols

Job description

AbbVie is seeking a Manufacturing Technician for the weekend shift to support GMP-compliant production, CAPA execution, and documentation in a sterile environment. The role requires working in a cleanroom and adhering to safety and quality standards, with cross-functional collaboration across teams.

Strong technical writing skills and the ability to prioritize tasks are essential. The position emphasizes maintaining isolator conditions, using the FMS system for data collection, and following