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Commissioning and Qualification Engineer
Eingestellt von Leap 29
Gesuchte Skills: Consultant, Engineering, Engineer
Projektbeschreibung
Commissioning and Qualification 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 commissioning and qualification engineers to work on the development of new facilities.
In this role, you will be working on a new Biotech facility. Initially the consultant will produce the protocols for commissioning and qualification. Once construction of the facility is completed, the consultant will begin carrying out the commissioning and qualification activities.
To be suitable for this 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 commissioning in a regulated Pharmaceutical environment
*Strong knowledge of Biotechnology facilities and equipment
*Experience of working in compliance with cGMP Standards
*Technical writing experience
Key responsibilities:
*Ensure the design intent has been achieved
*Work collaboratively with stakeholders, QA, system owners
*Writing and review of protocols and reports
*Start-up, commissioning and qualification (IQ/OQ/PQ) of the new facility
*Documentation development
*C&Q field execution, walk-downs and punch-list
In return you will be rewarded with a highly attractive hourly rate and a long term contract.
If you feel that you have the relevant skills and 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 commissioning and qualification engineers to work on the development of new facilities.
In this role, you will be working on a new Biotech facility. Initially the consultant will produce the protocols for commissioning and qualification. Once construction of the facility is completed, the consultant will begin carrying out the commissioning and qualification activities.
To be suitable for this 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 commissioning in a regulated Pharmaceutical environment
*Strong knowledge of Biotechnology facilities and equipment
*Experience of working in compliance with cGMP Standards
*Technical writing experience
Key responsibilities:
*Ensure the design intent has been achieved
*Work collaboratively with stakeholders, QA, system owners
*Writing and review of protocols and reports
*Start-up, commissioning and qualification (IQ/OQ/PQ) of the new facility
*Documentation development
*C&Q field execution, walk-downs and punch-list
In return you will be rewarded with a highly attractive hourly rate and a long term contract.
If you feel that you have the relevant skills and experience then please apply by following the relevant links provided.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Organisation/Management