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Quality Manager, Teamleader QA
Eingestellt von Experis AG
Gesuchte Skills: Support, Client
Projektbeschreibung
QUALITY MANAGER - STEIN - 100%
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based in Zuchwil, Experis is currently looking for a Quality Manager for a project until March 2018.
General information:
Start date: 02/10/2017
End date: 31/03/2018
Work location: Stein
Workload: 100%
Tasks & Responsibilities:
* Supervision of routine and stability testing for sterility, bioburden and bacterial endotoxin tests as microbiological analyses of sterile/low bioburden drug products and drug substances in time and in accordance to cGMP rules, QMs, SOPs and analytical test procedures.
* Supervision of routine and stability testing for microbial enumeration test as microbiological analyses of non-sterile drug products and drug substances in time and in accordance to cGMP rules, QMs, SOPs and analytical test procedures.
* Supervision of microbiological method validation/suitability studies.
* Ensure correct and timely investigation of microbiological deviations and other deviations (or OOE/OOS results) which influence the microbiological release of sterile/none sterile drug products and drug substances.
* Provides direct support to his/her team and decision making and oversight to ensure compliance to all standard operating procedures and documents.
* Preparation and support of authority inspections and participation as a microbiological expert.
* Manage the administrative aspects of the group by ensuring the preparation of job descriptions, performance management plans and conducting employee performance reviews.
* Collaboration on local projects.
You bring for this role the following qualifications:
* University or academic degree in microbiology, biochemistry, pharmacy or equivalent
* Minimum of 5 years relevant experience in the pharmaceutical manufacturing industry with at least 3 years in a leadership or supervision position
* Experienced understanding of cGMPs and other regulatory guidelines applicable to the pharmaceutical industry
* Fluent in German and English (spoken and written)
Interested in this opportunity?
Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Even though this position may not be the perfect fit for you, please reach out to us, as we have hundreds of open positions at Experis IT across Switzerland.
Experis is the global leader in professional resourcing and project-based workforce solutions. Our suite of services range from interim and permanent recruitment to managed services and consulting, enabling businesses to achieve their goals. We accelerate organisational growth by attracting, assessing and placing specialised professional talent.
For our international client based in Zuchwil, Experis is currently looking for a Quality Manager for a project until March 2018.
General information:
Start date: 02/10/2017
End date: 31/03/2018
Work location: Stein
Workload: 100%
Tasks & Responsibilities:
* Supervision of routine and stability testing for sterility, bioburden and bacterial endotoxin tests as microbiological analyses of sterile/low bioburden drug products and drug substances in time and in accordance to cGMP rules, QMs, SOPs and analytical test procedures.
* Supervision of routine and stability testing for microbial enumeration test as microbiological analyses of non-sterile drug products and drug substances in time and in accordance to cGMP rules, QMs, SOPs and analytical test procedures.
* Supervision of microbiological method validation/suitability studies.
* Ensure correct and timely investigation of microbiological deviations and other deviations (or OOE/OOS results) which influence the microbiological release of sterile/none sterile drug products and drug substances.
* Provides direct support to his/her team and decision making and oversight to ensure compliance to all standard operating procedures and documents.
* Preparation and support of authority inspections and participation as a microbiological expert.
* Manage the administrative aspects of the group by ensuring the preparation of job descriptions, performance management plans and conducting employee performance reviews.
* Collaboration on local projects.
You bring for this role the following qualifications:
* University or academic degree in microbiology, biochemistry, pharmacy or equivalent
* Minimum of 5 years relevant experience in the pharmaceutical manufacturing industry with at least 3 years in a leadership or supervision position
* Experienced understanding of cGMPs and other regulatory guidelines applicable to the pharmaceutical industry
* Fluent in German and English (spoken and written)
Interested in this opportunity?
Kindly send us your CV today through the link in the advert. However should you have any questions please contact Stéphanie Vogt.
Even though this position may not be the perfect fit for you, please reach out to us, as we have hundreds of open positions at Experis IT across Switzerland.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges