companion, we support you throughout the entire process, from the first contact to the first day on your new job – all this completely free of charge. Register now and look forward to many interesting and
SCHLAGHECK + RADTKE Executive Consultants GmbH sucht in eine/n Scientific Support Specialist w/m/d – LC-MS / MS / HPLC (ID-Nummer: 11545187)
companion, we support you throughout the entire process, from the first contact to the first day on your new job – all this completely free of charge. Register now and look forward to many interesting and
Management of the global IT CoE Quality System: personnel management and financial responsibility for cost centres Determining requirements and advising on IT requirements in the ‘Quality’ area. Support in the
, Financial Controls Manual (FCM) and SOX 404 requirements Support SOX 404 attestation processes Understand business processes; review process documentation and have a good understanding of key risks and
and experience. All aspects of user and license management including new user setup/deactivation, roles, profiles, permissions, public groups User support tickets Identify and gather requirements from
on the dotted line or having your application rejected. Register with us and reap the benefits of interesting job offers that match your skills and experience. Legal support to contracts – 3rd party
and experience. Plan and implement IT technologies to support business processes Manage IT, OT and infrastructure technologies for pharmaceutical manufacturing sites Create operating models for the
companion, we support you throughout the entire process, from the first contact to the first day on your new job – all this completely free of charge. Register now and look forward to many interesting and
and experience. Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility
Development: Establish and maintain process infrastructures to support clinical research activities Process Oversight and Quality Management: Monitor and manage clinical research processes to ensure quality and
for the batch record review e.g. Analysis Reports, Specifications for clinical development, country label approval etc. Support the timely release of GMP batches of labels, primary packed materials and
lab infrastructure and supports order and housekeeping of chemicals and reagents required Requirement is successful completion of a relevant apprenticeship (focus analytics) or university degree in a
and experience. Perform demand analysis for new laboratory space demands in the Divisional portfolio in accordance with our process, and incorporate process improvements to the process Support ongoing