Beschreibung
Tasks:
- Supporting the Basel and global IT Organization in compliance and Quality Management, for GxP or non GxP applications and IT Infrastructure.
- The assessment, facilitation and verification of quality standards achieved within IT activity in a designated geographic/operational area in accordance with the requirements of the customers corporately and any external legislative or regulatory requirements.
- Applies the specifications of the corporate and organizational Quality Systems and Quality standards to ensure that the quality of processes and deliverables of both, projects and services continuously meet their specified corporate and regulatory requirements.
- Follow up resolution of identified quality exposures and escalation to line management if critical situations are not resolved in due course.
- Contribute to business decisions in the definition and assessment of IT requirements.
- Support the development and delivery of training in quality matters.
- Drive and facilitate the creation of relevant SOPs.
- Interface with business and IT partners to ensure Novartis practices are aligned with regulatory expectations and industry best practices.
- Prepare, or review and approve major system documentation to ensure consistency with quality standards and quality of deliverables.
- Coordinates documentation, testing, and change management activities to ensure compliance with business and regulatory needs.
Requirements:
- +7 years experience of quality management
- Pharmaceutical industry experience together with a good understanding of processes/organization etc.
- Team work in a challenging IT environment
- Flexibility and experience in prioritizing tasks
- Ability to deal with variable workload
- Experience of GxP practices.
- Experience of ITIL 2 or 3.
Location: Switzerland - Basel
Duration: ASAP - 31.12.2014
Assistance will be provided for obtaining Swiss Work Permit, Housing, and opening Swiss Bank account.
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