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Manufacturing Support Technician

AbbVie Inc.
Ballytivnan, Sligo, Ireland
On-site

About this role

About the Role

We are seeking a Manufacturing Support Technician to join a brand new team at AbbVie's Ballytivnan site in Sligo. This onsite role supports biologics operations, with shift work and emphasis on safety, regulatory compliance, and quality in line with cGMP requirements. What You'll Do

  • Work as a team member to support biologics operation in pharma operations in line with all safety, regulatory and organizational requirements.

  • Be assigned to daily production operations, operating different equipment.

  • Document all activities in line with cGMP requirements.

  • Efficiently operate all biologics processes minimizing material loss.

  • Perform intermediary packaging where applicable.

  • Assemble and inspect equipment in the manufacturing area to confirm operational status.

  • Perform in-process testing methods.

  • Monitor process alarms.

  • Receive materials from warehouse, verifying documentation.

  • Transfer final material to warehouse inventory.

  • Perform process tests and participate in qualification and validation activities as required.

  • Ensure manufacturing documentation is completed on time and without errors following cGMP.

  • Diagnose and resolve events or exceptions of production equipment and processes.

  • Dispose of domestic, biomedical, and hazardous waste per regulations and site policies.

  • Maintain detailed records of operations, manually or electronically, for the shift.

  • Participate in Factory Acceptance Testing, Site Acceptance Testing, commissioning and equipment qualification.

  • Adhere to Quality & Safety policies.

  • Support external inspections and internal audits.

  • Assist in developing batch records and electronic batch records.

  • Collaborate with Engineering, Quality and other departments to develop and update SOPs. What We're Looking For

  • 3rd level qualification in a relevant Science discipline OR 2 years of experience in a GMP environment.

  • Previous experience in GMP environment (medical device or Pharma).

  • Flexibility, strong concentration and attention to detail.

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