Description:
We’re currently recruiting for an exciting opportunity with an award-winning Biopharmaceutical organization based in the north Dublin area. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Responsibilities.
- Work with the manufacturing operations group, project design team, the CQV team, the Automation/CSV reps to facilitate the development and validation of the manufacturing facility.
- Support Equipment Design/ HAZOP and Room programming reviews.
- Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g., EHS metrics, Production Plan, OEE, compliance and team training.
- Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.
- Generate SOPS/Electronic Batch Records.
- Adhere to Right First-Time principals.
- Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
- Escalate issues as appropriate to Process Lead
Required Knowledge and Experience:
- Team worker.
- Ability to work cross functionally and with multiple stakeholders.
- Trouble shooting capabilities.
- Understanding of Drug Substance Manufacturing Operations.
- Understanding of GMP requirements in a Bio-pharmaceutical Facility.
- Excellent communication skills.
- Ability to multitask.
- A level 6 with a minimum of 3 years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.
- Minimum of a Level 7 qualification in a science or engineering discipline.