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Technical Writer
Eingestellt von Quanta Consultancy Services
Gesuchte Skills: Engineering
Projektbeschreibung
A global pharmaceutical industry leader is currently seeking an experienced Technical Writer to join their site in Switzerland. The site is currently undergoing a lot of new investment so this is an excellent opportunity and an exciting time to join this site.
Project:
The Technical Writer is required to be responsible for the authoring of SOPs on a global Track and Trace roll-out on all packaging equipment. A number of technical and IT related SOPs will need to be written for each new piece of equipment.
Location: Basel area, Switzerland.
Duration: Two years
Responsibilities will include, but are not limited to:
Write SOPs for each new piece of equipment AND associated IT systems.
Adapt vendor SOPs to fit in with Production site use.
Ensure equipment and instructions are properly handed over to the users in the production department.
Ensure GMP compliance.
Skills and Experience:
Fluent German and English are absolutely essential.
The ideal candidate will come from an equipment engineering or IT (Pharma) Background.
Experience of writing technical documentation
Experience of working compliantly within GMP guidelines.
The successful candidate will be a self-starter and a team player, as well as being methodical, conscientious and thorough.
This is a fantastic long-term opportunity, which offers, for the right candidate, the possibility of home-working. The position is paying a very competitive Hourly Rate.
Project:
The Technical Writer is required to be responsible for the authoring of SOPs on a global Track and Trace roll-out on all packaging equipment. A number of technical and IT related SOPs will need to be written for each new piece of equipment.
Location: Basel area, Switzerland.
Duration: Two years
Responsibilities will include, but are not limited to:
Write SOPs for each new piece of equipment AND associated IT systems.
Adapt vendor SOPs to fit in with Production site use.
Ensure equipment and instructions are properly handed over to the users in the production department.
Ensure GMP compliance.
Skills and Experience:
Fluent German and English are absolutely essential.
The ideal candidate will come from an equipment engineering or IT (Pharma) Background.
Experience of writing technical documentation
Experience of working compliantly within GMP guidelines.
The successful candidate will be a self-starter and a team player, as well as being methodical, conscientious and thorough.
This is a fantastic long-term opportunity, which offers, for the right candidate, the possibility of home-working. The position is paying a very competitive Hourly Rate.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik