Description
A global pharmaceutical company are looking for a Quality Specialist - 3rd Party Contract Manufacturing for a 12 Month Contract + to be based in Switzerland.You will report to 3rd Party Manufacturing Manager - who manages 3rd party contract manufacturing for development activities
The Role:
-Support the activities related to 3rd party contract manufacturing and labs.
-Audit work - Assist in follow up action investigation - assist in follow up of main audits
-Ideally someone who has experience of working on AQWA or the QARP pharma technology
-This role is about auditing and face to face meetings
Experience
-Experience in Quality Assurance
-Good exposure of working on an international level
-Good understanding of requirements from Regulatory Agencies
-Experience with 3rd party contract manufacturing - will be dealing with contract facilities as well as contract laboratories
-English only
-Some travel maybe required in the future - manager is doing all the travelling
Summary
-Really wants someone who has worked/experienced in the QA realm
-Auditing experience - within follow up
-Experience of working on an international level with 3rd party management
-Clinical and development background / understanding
Please apply for more details.