IT Quality Validation Expert - Quality Assurance

Are you a mid-level QA/quality analyst with in-depth knowledge of IT Quality processes and governance (eg GAMP 5 and ISO 13485), experience writing SOPS and designing processes, experience with LEAN processes, and exposure to Electronic Document Management Systems?

Are you fluent in English?

Do you want to work on a highly technical project in a multinational environment in Basel?

Are you available to start work in Basel on or before 15th February and work until 31/07/2016?

If you have answered yes to these 4 questions then we have a contract assignment available within a major pharmaceutical company just for you...

Key tasks:

60% Support the IT Quality Validation & Governance Team in the creation of directives and SOPS across functions
20% Document Librarian. Proofread and prepare documents for approval. Initiate, track and manage document workflows across projects. Initiate training for new team members.
20% Provide support to the Quality Team in organizing, facilitating, and documenting trainings, workshops, and initiatives.
Support for US EST Time Zone is possible, therefore flexible working hours may apply

Essential skills and experience:

Mid-level QA/quality analyst experience with in-depth knowledge of IT Quality processes and governance eg GAMP 5 and ISO 13485
Experience writing SOPS and designing processes in a complex, fast paced environment
Experience in LEAN processes a plus
Experience with Electronic Document Management Systems
Experienced with MS Word, MS Powerpoint, and Visio
Proficient English language skills and experience working on aglobal cross-cultural team
Experience with pharmaceutical environment

If you meet these requirements and are interested in working for a multinational pharmaceutical organisation, please send your CV as soon as possible. Interviews will be taking place on 2nd February so please do not delay.