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QA Associate
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Support, Client
Projektbeschreibung
For our client in ROTKREUZ we are looking for a QA ASSOCIATE for a 7-MONTH project.
DURATION: 01/06/2018 TO 31/12/2018
LOCATION: ROTKREUZ
WORKLOAD: 50%
ABOUT THE ROLE:
Support the head of quality on daily activities. Ensure that products are received, stored, handled, released, distributed and transported according to labelled regulatory and GxP requirements.
MAJOR ACTIVITIES:
. Timely and compliant handling and approval of product returns
. Support QA Head on product release
. Ensure compliant archiving of GxP Documents
. Ensure trainings of the CH associates are completed on time
. Gather maintaining and report Key Quality Indicators in accordance with division quality requirements
. Is obligated to report any complaint (eg, Adverse Event or Quality complaint) within 24h from the receipt to the Regulatory Affairs department in accordance to the valid local SOPs.
Ideal Background:
Education (minimum/desirable):
. BS degree in scientific discipline or equivalent experience in pharmaceutical environment
Languages:
. Fluent in German and English
Experience/Professional requirement:
. At least 3 years in a pharmaceutical environment, preferably in QA. Experience in batch release. Experience in medical devices requirement is a plus
For further details please contact Beata Arciszewska.
DURATION: 01/06/2018 TO 31/12/2018
LOCATION: ROTKREUZ
WORKLOAD: 50%
ABOUT THE ROLE:
Support the head of quality on daily activities. Ensure that products are received, stored, handled, released, distributed and transported according to labelled regulatory and GxP requirements.
MAJOR ACTIVITIES:
. Timely and compliant handling and approval of product returns
. Support QA Head on product release
. Ensure compliant archiving of GxP Documents
. Ensure trainings of the CH associates are completed on time
. Gather maintaining and report Key Quality Indicators in accordance with division quality requirements
. Is obligated to report any complaint (eg, Adverse Event or Quality complaint) within 24h from the receipt to the Regulatory Affairs department in accordance to the valid local SOPs.
Ideal Background:
Education (minimum/desirable):
. BS degree in scientific discipline or equivalent experience in pharmaceutical environment
Languages:
. Fluent in German and English
Experience/Professional requirement:
. At least 3 years in a pharmaceutical environment, preferably in QA. Experience in batch release. Experience in medical devices requirement is a plus
For further details please contact Beata Arciszewska.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges