Validation Consultant - Medical Devices

Solothurn  ‐ Onsite
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Description

Our client is currently looking on an experienced quality engineer to support a project related to validation and verification activities.
RESPONSIBILITIES:
  • Strong engineering skills with working knowledge of Process validation/verification activities
    * Ability to use Quality Engineering principles, tools, and practices to develop and optimize systems and processes that are aligned with the overall business and quality.
    * Problem solving techniques including 8D, root cause analysis and cause and effect analysis. Experience in CAPA execution and management.
    * experience is required, preferably within a regulated environment (e.g. FDA, ISO 13485 regulated), ideally in Med-tech.
    * Experience in Change Control, Manufacturing/Product Transfers, Outsourcing Initiatives
    * Experience with project management.
    EXPERIENCE REQUIREMENTS:
  • Degree in Engineering, or in a related technical/scientific discipline is required.
    * Ability to work independently and partner with a cross-functional team (supplier, R&D, Regulatory, Manufacturing, and Purchasing etc).
    * Excellent written and oral communication skills.
    * Ability to provide regular updates to project leader and team at various forums
    * Organizational talent, reliability, dependability, personal initiative, customer / service orientation.
    * Working knowledge of Microsoft office products (Word, Excel, Access, and Project etc).
    * Language: English and German mandatory


Please contact Serena:

Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Start date
07/2019
Duration
12 months
From
Michael Bailey Associates
Published at
01.06.2019
Project ID:
1778959
Contract type
Freelance
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