Description
We are currently working with a World leader in Medical Devices who are looking to bring on a Validation Engineer on a 12 month Contract ASAP. The successful candidate will play a key role in the planning and execution of validation activities related to new product introductions, product transfers and process changes. Provide support for the Validation activities associated with equipment & processes ensuring that all compliance issues & requirements of Company validation policies and procedures are addressed. Below is a list of the Successful Candidates duties.- Act as Subject matter Expert on the validation process for the site
- Contribute to the planning and execution of validation activities related to new product introductions, product transfers and process changes.
- Works as an integral member of project teams to provide guidance and support in establishing optimal validation approach and/or strategy.
- Provide technical assistance to carry out problem solving analysis/ root causing investigation.
- Create, execute and review validation related documents, including but not limited to: Protocols, Reports, Change controls, Validation Plans, etc.
Key competencies required
- Excellent communications skills
- Pro-active approach to work
- Crossfunctional Team Player
- Flexible & Adaptable
- Highly computer literate
- High attention to detail
- High Work standards
Essential Experience
- Degree Engineering/Science discipline
- Minimum 3-5 year's experience in quality assurance/engineering (a minimum of 2 years of which has been spent carrying out validation
- Experience in generation of pFMEA
- Understanding of Statistical techniques for assessment of process capability
- Ability to interpret Engineering drawings/specifications
- Familiarity in areas of various inspection techniques
- Excellent interpersonal & communication skills
For more information on this role please contact Jamie McLaren on
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