▷ (2/6/2025 A) Senior Validation Engineer

5 hours ago


Dublin, Ireland PE Global (UK) Full time

PE Global is currently recruiting for a Downstream Bioprocess Associate for a leading multi-national Biotech client based in Dublin North.

This is an initial 11-month contract 4 Cycle Shift role – 7 to 7, working 2 days 2 nights followed by 4 rest days.

ROLE:

- Work with the manufacturing operations group, project design team, the CQV team, the Automation/CSV reps to facilitate the development and validation of the facility manufacturing facility.
- Support Equipment Design/ HAZOP and Room programming reviews as per requirements.
- 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.
- Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
- Generate SOPS/Electronic Batch Records for start-up.
- Adhere to Right First-Time principles.
- Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
- Escalate issues as appropriate to Process Lead.
- Maintain a high level of personal expertise and working knowledge of all aspects of the manufacturing process and process equipment through continuous training and development.
- Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan.

REQUIREMENTS:

- Minimum of a Level 7 qualification in a science or engineering discipline.
- A level 6 with a minimum of 3 years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.

Interested candidates should submit an updated CV.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.***

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