Quality Validation Engineers

Proclinical is advertising a vacancy for a Quality Validation Engineer position with a leading pharmaceutical company. The organization is dedicated to ensuring that tens of thousands of people with rare and serious diseases are able to live normal, healthy lives. Based in the company's Illinois office, this is an exciting opportunity to work with a dynamic and innovative company.

Job Responsibilities:

• Inspecting newly installed equipment and software to ensure they reach GMP standards; performing technical interpretations from a quality assurance/validation background to make sure they fit in with site culture and QA standards.
• Reviewing, approving, and signing off on all the work with the company engineers, from a QA perspective.
• Validating the Siemens system to ensure it is up to QA code and fits into QA standards.
• Performing Gap Analysis.
• Ensuring documents meet GMP standards.

Skills and Requirements:

• Experience with QA.
• Experience with Siemens 7.
• Demonstrable understanding of system URS.
• Experienced in ensuring documents meet GMP standards.
• Demonstrable multitasking, project management, and execution skills.
• Good interpersonal skills, including communication, presentation, persuasion, and influence.
• Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
• Proficiency with computer skills, such as MS Office.

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Keri Marshall at +44 207 440 0679 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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