Manufacturing Support Technician

Job Description

We are recruiting a Manufacturing Support Technician to join a brand new team on our site in Ballytivnan, Sligo. You will work as a team member to support biologics operations in pharma operations in line with all safety, regulatory and organizational requirements.

This role will require shift work.

Responsibilities:

• To work as a team member to support biologics operations in pharma operations in line with all safety, regulatory and organizational requirements.
• Manufacturing Support Technician will be assigned to the daily production operations operating different equipment.
• Documentation of all activities in line with cGMP requirements.
• Efficiently operate all biologics processes minimizing material loss.
• Perform product intermediary packaging, as applicable.
• Assemble and inspect equipment in the manufacturing area to confirm its operational status.
• Perform all in process testing methods.
• Monitor Process Alarms.
• Material receipt from warehouse, verifying all pertinent documentation.
• Transfer of final material to warehouse inventory.
• Perform process tests and participate in qualification and validation activities as required. Ensure all manufacturing documentation is completed on a timely manner without errors, following cGMP's.
• Diagnose and resolve events or exceptions of production equipment and processes.
• Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulations following the procedures and policies of the plant, division, and the corporation.
• Keep detailed records, manual or electronic, of the operations carried out during the work shift.
• Active Participation in Factory Acceptance testing, Site Acceptance Testing and commissioning and qualification of equipment.
• Adhering to all relevant policies relating to Quality & Safety.
• Ensure successful external inspections, and Division and Corporate audits.
• Active participant in the development of batch records and electronic batch records for the site. Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures.

Qualifications

• 3rd level qualification in a relevant Science discipline OR 2 years of experience in a GMP Environment
• Previous experience in a GMP environment (med device or Pharma)
• Flexibility, great concentration & attention to detail

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 only - to learn more, visit

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: