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Validation Engineer
Eingestellt von Leap 29
Gesuchte Skills: Engineer, Consultant, Engineering
Projektbeschreibung
Validation Engineer
My client is an international pharmaceutical company that develops innovative medicines to treat many of the world's most serious and widespread illnesses. They are in need of validation engineers to work on the development of new facilities.
In this role, you will be working on a new Biotech facility in Ireland. Initially the consultant will produce the plan and protocols for validation. Once the commissioning phase of the pharmaceutical facility is completed, the consultant will begin carrying out the validation activities.
To be suitable for the Validation Engineer position you will need to have the following background:
*Minimum of degree qualification in relevant science and/or engineering discipline
*Minimum 10 years' experience of validation in a regulated Pharmaceutical environment
*Strong knowledge of Pharmaceutical facilities and equipment
*Experience of working in compliance with cGMP Standards
*Technical writing experience
Key responsibilities of the Validation Engineer:
*Develop and approve Validation Plans and procedures.
*Provide guidance on the Validation strategy.
*Writing and review of the Validation Protocols (Facility, Process, Clean, Equipment etc.)
*Writing and review of the Validation reports
*Resolve and close out of issues identified during qualification execution.
*Ensure that change requests are compliant with all applicable procedures.
In return, the Validation Engineer will be rewarded with a highly attractive hourly rate and a long term contract.
If you feel that you have the relevant skills and pharmaceutical experience then please apply by following the relevant links provided.
My client is an international pharmaceutical company that develops innovative medicines to treat many of the world's most serious and widespread illnesses. They are in need of validation engineers to work on the development of new facilities.
In this role, you will be working on a new Biotech facility in Ireland. Initially the consultant will produce the plan and protocols for validation. Once the commissioning phase of the pharmaceutical facility is completed, the consultant will begin carrying out the validation activities.
To be suitable for the Validation Engineer position you will need to have the following background:
*Minimum of degree qualification in relevant science and/or engineering discipline
*Minimum 10 years' experience of validation in a regulated Pharmaceutical environment
*Strong knowledge of Pharmaceutical facilities and equipment
*Experience of working in compliance with cGMP Standards
*Technical writing experience
Key responsibilities of the Validation Engineer:
*Develop and approve Validation Plans and procedures.
*Provide guidance on the Validation strategy.
*Writing and review of the Validation Protocols (Facility, Process, Clean, Equipment etc.)
*Writing and review of the Validation reports
*Resolve and close out of issues identified during qualification execution.
*Ensure that change requests are compliant with all applicable procedures.
In return, the Validation Engineer will be rewarded with a highly attractive hourly rate and a long term contract.
If you feel that you have the relevant skills and pharmaceutical experience then please apply by following the relevant links provided.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Organisation/Management