AbbVie

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 to implement improvements in the quality, safety
Execution of commissioning and validation protocols on an ongoing basis.

🎯 Requirements

Leaving Cert or similar
Experience of operating in a highly automated environment.
Good I.T. skills are required.

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