Pharma Manufacturing Technician: cGMP & Automated Ops

AbbVie; Sligo; On-site; EUR 35,000 - 45,000; Full time

Job summary

AbbVie is seeking a Pharmaceutical Technician on site in Manorhamilton Road, Sligo for a 12 month fixed-term contract. This role involves rotational shift work and responsibilities in producing drug product materials while adhering to compliance requirements.

Your duties will include coordinating team activities, documenting processes in line with cGMP, and participating in continuous improvement programs. A 3rd level qualification in Engineering or Science is preferred, or 2+ years experience in a GMP environment is acceptable.

Qualifications

• 3rd level qualification, preferably in Engineering or Science related fields OR 2+ years in a GMP regulated environment.
• Experience of operating in a highly automated environment.
• Good I.T. skills are required.

Responsibilities

• Pharmaceutical processing activities in our manufacturing building and support locations.
• Team co-ordination to maximise the effectiveness of the team members.
• Documentation of all activities in line with cGMP requirements.
• Cross training within the team and training of new team members.
• Participation in continuous improvement programs.
• Execution of commissioning and validation protocols.
• Maintaining the overall cGMP of the pharmaceutical processing areas.
• Adheres to and supports all EHS & E standards, procedures, and policies.

Skills

Good I.T. skills

Experience in automated environment

Education

3rd level qualification in Engineering or Science

Job description

AbbVie is seeking a Pharmaceutical Technician on site in Manorhamilton Road, Sligo for a 12 month fixed-term contract. This role involves rotational shift work and responsibilities in producing drug product materials while adhering to compliance requirements.

Your duties will include coordinating team activities, documenting processes in line with cGMP, and participating in continuous improvement programs. A 3rd level qualification in Engineering or Science is preferred, or 2+ years experience in a GMP environment is acceptable.