Validation Specialist - Contract - wide work responsibility.

If you enjoy working with validation and risk assessment, then this can be for you. I am currently working with a client who is looking to fill a 12 month contract for a Validation Specialist role. As past of your role you will be working with computerization system validation, risk assessment and summary reports of the different projects that the company is undergoing. This width of your work responsibilities will give you the chance of expanding your knowledge, which can open up for more possibilities when applying for you next job.

You will be working with a well known company who are working in innovative ways in order to give you opportunities for future applications. Because this is a global company and they invest in their employees, there can be opportunities for relocation depending on your preferences. Their investment in you means that you can feel secure during your time working with my client. You will gain much experience, and be able to develop yourself as much, opining up different opportunities for when you apply in the future.

Requirements:
* 2 years Validation experience
* FDA knowledge,
* GMP, 21 CFR, and USP 1058 knowledge.
* Technical report writing skills.

If you are interested in the Validation area and would like to hear more about this opportunity to do hesitate to call me Maren Asheim on +41 435080816 or send me an email for when you are most available on M.Asheim@nonstop-recruitment.com.