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Technical Writer
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Client
Projektbeschreibung
For our medical device client in Bern, we are looking for a Technical Writer for a contract role.
In this position you are responsible for writing and revision of Quality Control process documents such as standard operating procedures, work instructions and job aids as well as test method instructions and protocols.
You will mainly revise existing procedures and instructions thereby implementing the gathered feedback from scientific experts, EHS, QA and QS. A profound knowledge of analytical test methods will help you to challenge the status quo. Improvements shall be implemented to test instructions and the ability for complete and unambiguous documentation on protocols be given. You will profit from your knowledge of cGMP requirements to ensure the compliant definition of QC process. Most importantly you have good writing skills ensuring the clarity of processed documents to the audience.
Your team spirit will allow you to integrate into the team and interact with stakeholders from EHS, QA and QS.
Tasks:
* Revision of existing of test instructions and protocols of analytical methods
* Ensuring the compliance of analytical test methods with EHS, pharmacopeia and cGMP requirements
* Collecting and implementing stakeholder feedback for test methods instruction from scientific experts, EHS, QA and Quality Systems
* Revision of existing and writing of new SOPs for QC processes
* Ensuring the compliance of QC processes with global and local guidelines and procedures as well as with legal and regulatory requirements
* Collecting and implementing stakeholder feedback for QC process documents from EHS, QA and Quality Systems
* Translation of German documents into English and vice versa
Qualifications
* Knowledge of chemical, biochemical and microbiological analytical methods
* Knowledge of cGMP requirements for QC processes
* Laboratory experience in a cGMP regulated environment
* Excellent verbal and written skills in German and English
* Experience in using MS Office software is required
* Experiences in writing document standards and processes instructions is required
* Experience using document management software is required
* Teamplayer and good communication skills
* German and English required
Would you like to apply for this job opportunity?
Please send me your updated CV or feel free to contact me
I am looking forward to hearing from you.
In this position you are responsible for writing and revision of Quality Control process documents such as standard operating procedures, work instructions and job aids as well as test method instructions and protocols.
You will mainly revise existing procedures and instructions thereby implementing the gathered feedback from scientific experts, EHS, QA and QS. A profound knowledge of analytical test methods will help you to challenge the status quo. Improvements shall be implemented to test instructions and the ability for complete and unambiguous documentation on protocols be given. You will profit from your knowledge of cGMP requirements to ensure the compliant definition of QC process. Most importantly you have good writing skills ensuring the clarity of processed documents to the audience.
Your team spirit will allow you to integrate into the team and interact with stakeholders from EHS, QA and QS.
Tasks:
* Revision of existing of test instructions and protocols of analytical methods
* Ensuring the compliance of analytical test methods with EHS, pharmacopeia and cGMP requirements
* Collecting and implementing stakeholder feedback for test methods instruction from scientific experts, EHS, QA and Quality Systems
* Revision of existing and writing of new SOPs for QC processes
* Ensuring the compliance of QC processes with global and local guidelines and procedures as well as with legal and regulatory requirements
* Collecting and implementing stakeholder feedback for QC process documents from EHS, QA and Quality Systems
* Translation of German documents into English and vice versa
Qualifications
* Knowledge of chemical, biochemical and microbiological analytical methods
* Knowledge of cGMP requirements for QC processes
* Laboratory experience in a cGMP regulated environment
* Excellent verbal and written skills in German and English
* Experience in using MS Office software is required
* Experiences in writing document standards and processes instructions is required
* Experience using document management software is required
* Teamplayer and good communication skills
* German and English required
Would you like to apply for this job opportunity?
Please send me your updated CV or feel free to contact me
I am looking forward to hearing from you.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung