Validation Consultant - Medical Devices

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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 mandatoryPlease contact Serena: 02077495631Michael Bailey International is acting as an Employment Business in relation to this vacancy.