A detailed plan has to be created for the migration of 133 PC’s in the timeframe 2016-2017. A dedicated team will be installed that has to deliver this plan during Q4 2015 and Q1 2016. The plan has to contain a detailed proposal for each system, if upgrading or migrating is required, if new hardware and/or equipment has to be procured and what qualification/validation approach has to be applied.
Provide detailed assessment of all PCs (guidance doc available)
Establish qualification / validation documentation
Execute compliance testing
Advise in case of non-compliances
Ensure working according to guidelines
Ability to influence and communicate with all levels of the organization
Good communication skills
Proactive and high level of stamina
Experience in project management
Minimum BSc in IT / automation
Knowledge of and experienced in working with GMP equipment
Knowledge of lab automation and/or process automation
Minimum of three years’ experience
Must have a high standard for compliance
Experience with maintaining or implementing software and equipment within a regulated environment (i.e. pharma)
Reactie is prive en alleen zichtbaar voor de opdrachtgever en de plaatser van de reactie.
Je moet inloggen voordat je een reactie kunt plaatsen.