Senior Automation IS Engineer

Noord-Brabant  ‐ Onsite
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Description

Automation IS Engineer required to join a global pharmaceutical company located in the Netherlands for a 12 month initial contract.

The senior automation IS project engineer will provide support for computerised systems in a GMP (Good Manufacturing Practices) regulated atmosphere and will be responsible for deploying software, incident management, life cycle management, system maintenance including application upgrades, projects, enhancements and security patches. Your proven overall IT and engineering knowledge, communication skills and project Management experience will enable you to liaise effectively with clients, users and IT experts (application, network, database, etc.) locally, as well as with other sites worldwide in order to provide IT solutions for clients.

The Senior automation IS project engineer will co-ordinate small projects or serve as a project member on larger projects. He/she will have the discipline and technical knowledge to work independently and take on responsibilities, as well as design and deploy new innovative solutions to improve the efficiency of business processes and ensure procedures are followed and new systems are implemented in compliance with FDA/EMA and other regulatory requirements. Will work with other IT and engineering experts, vendors and customers to ensure regulatory (eg validation), business, functional and application specific requirements are met.

Functional Responsibilities
  • Maintains in depth knowledge of information systems technology and engineering
  • Mentors and trains department staff members
  • Demonstrates knowledge about IT and Engineering processes.
  • Participates in evaluating business applications and processes. Able to recognise problems and communicate solutions conceptually
  • Collaborates with client representatives to collect and analyse changes required to business applications
  • Responsible for acting as the primary interface with the client to establish all connectivity between organisations
  • Translates requirements into technical solutions that meet business needs
  • Facilitates process mapping sessions for complex business processes
  • Facilitates the implementation of new programs and processes in client area
  • Creates project artefacts according to project requirements
  • Reviews and approves project documentation
  • Maintains knowledge of IS quality and compliance policies, SOPs and associated documents
  • Support, participates in and responds to questions and findings from regulatory and other audits
Requirements:
  • 10 years of Information Systems (IS) experience preferable within the pharmaceutical or biotech industry.
  • 10 years of experience with installing, testing and deploying new IT solutions in an Engineering environment
  • Experience in automation or equipment engineering combined with Information Systems (IS)
  • Experience as a project-manager in implementing IT solutions on an application level
  • Builds, leads, and coaches project teams throughout project life cycles
  • Experience in use of MS Project (project scheduling, time management)
  • Knowledge of change management and validation of computerized systems (eg GAMP5)
  • Experience in developing and executing SOPs, Installation and Operational (IQ, OQ) Protocols
  • Fluent in English (both verbal and written)
Start date
ASAP
Duration
Initially 6 months
From
Quanta Consultancy Services
Published at
19.04.2016
Project ID:
1113641
Contract type
Freelance
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