Job Detail

Introduction

ALTEN, the European leader in engineering and technology consulting, provides support for its clients’ development strategies in the fields of innovation, R&D and it systems. Its 28.000 top engineers carry out studies and conception projects for the technical and information systems divisions of large corporate clients in the industrial, telecommunications and services sectors. In a fast globalising world, ALTEN integrates with the R&D strategy of its clients to support performance and partner them in breaking into new markets. ALTEN is active in 20 countries, covers the whole development cycle and offers a choice of service levels, from technology consulting to full-blown project outsourcing. It is the technology partner of choice for Europe’s leading companies.

Due to the growth of the business activity, from the International Talent Acquisition Department, we are now looking for a QA Systems Engineer to join our team in the Life and Science Industry in the French speaking part of Switzerland.

We are looking forward to getting to know you and your ambitions!

Responsibilities

• Support the International Project Leads in coordinate activities and task related to the projects


• Follow up of project actions


• Support with communication about project progress to the different organization groups


• Help with the mapping and verification of documents


• Coordinate logistics related to system users training


• Review and update GMP/GDP documentation as per project needs


• In collaboration with the different sites and departments ensure appropriate document categorizations and attributes definition


• Prepare monthly training metrics and presentation for management review for Sites and Affiliates


• Contribute to the metrics optimization for Documentation and Training


• Follow up on Training Compliance of International GPDO employees


• Ensure Compliance of documentation periodic review process

Skills

• Economic or administrative degree or equivalent training/education


• A minimum of 5 years of working experience in a pharmaceutical company or other related industry


• Experience in handling of GMP/GDP/Quality documentation


• Knowledge in Electronic Documentation Systems is an asset


• Fluent in French and English


• Ability to work independently and to be operational very quickly