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

• 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.