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Production operator

Dublin
Life Science Recruitment
Production operator
Posted: 27 July
Offer description

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Production Operator
11 Months
AS22481

We're currently recruiting for 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.
The role will be responsible for the preparation, operation and monitoring of equipment, use of business systems and carrying out tasks including but not limited to the cleaning, validation, in-process testing and basic maintenance of equipment in accordance with current Good Manufacturing Practices (cGMPs).

Duties: 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.Production Operator
11 Months
AS22481

We're currently recruiting for 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.
The role will be responsible for the preparation, operation and monitoring of equipment, use of business systems and carrying out tasks including but not limited to the cleaning, validation, in-process testing and basic maintenance of equipment in accordance with current Good Manufacturing Practices (cGMPs).

Duties: 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.Education and Experience: Experience in a GMP Manufacturing environment required.Level 7 qualification in a science or engineering discipline.Understanding of Drug Substance Manufacturing Operations beneficial.If interested in this posting please feel free to contact Avishek Singh at ****** or 0872827991 for further information.
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