Key Responsibilities:
* Facilitate the development and validation of manufacturing facilities.
* Support equipment design, HAZOP reviews, and room programming.
* Execute commercial manufacturing processes according to established work instructions and SOPs.
* Generate SOPS and Electronic Batch Records.
About the Role:
This is an exciting opportunity with a pharmaceutical organisation based in Dublin.
The role will be responsible for all procedures and processes associated with the manufacture of Commercial Large-Scale Drug Substance at the manufacturing facility.
Duties include working with the manufacturing operations group, project design team, CQV team, and Automation/CSV reps to facilitate the development and validation of the manufacturing facility.
Required Skills and Qualifications:
* Experience in a GMP Manufacturing environment required.
* Level 7 qualification in a science or engineering discipline.
* Understanding of Drug Substance Manufacturing Operations beneficial.
Benefits:
We're currently recruiting for this exciting opportunity.
If you're interested in this posting, please feel free to contact us for further information.