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Job Details
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CSV Specialist - Take your career to the next level



Business Type: Healthcare - Management Consultancy, Internet - IT Services
Job Type: Quality Assurance - Control, Validation, Information Technology, Consultant
Job Level: Experienced (non manager)
Position: Full Time
Salary: CHF120000 - CHF135000 per annum
Location: Switzerland
Reference: EM/CSV/07
Closing Date: 15/02/19
Job Details:

My client is well known in it''s market for the outstanding professionalism and and ethical approach to business. Simply put, they employ the best talent in the field and thus get the best projects.

The best projects getting completed successfully by you and your team means that you have a golden opportunity to expand your network with some of the most important names in the industry.

Their employees come first as they recognise that through them, they keep the client satisfied and thus business grows. As a result, they work with flat hierarchies.

If you feel that so far this is the place for you, here''s what you can expect from the role and what they expect from you:

Your tasks

Management / implementation of demanding and diversified consulting projects in information technology (Efficient IT and CSV / cGxP) for our customers in the life science industry
Development and implementation of individual IT / CSV consulting concepts
Technical support of our customers in ongoing validation projects, in particular in IT system validation (eg for ERP, MES, LIMS systems or laboratory / analytical equipment)
Professional support in the creation of life-cycle documents
Active assistance in the acquisition of new customers and projects
Participation in the professional development of the department
your profile
completed scientific or engineering studies (pharmaceutical, process engineering, chemistry or equivalent) or business informatics
Practical experience and very good knowledge in quality management and / or validation of ERP, MES, LIMS and other IT systems (eg SAP, Microsoft Dynamics, Infor M3, GUS-OS, WinLIMS etc.)
Practical knowledge of GAMP 5 ©, 21 CFR Part 11/210/820, FDA, EU GMP, Annex 11/15, as well as ISO9000ff, ISO13485 and others.
Willingness to international travelling and participation in international teams
German and English language skills (oral and written).



Posted: 08/02/2019 | NPJ Ref: 230215
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