CSV Remediation Engineer

Are you interested or looking for your next CSV project in the Pharmaceutical industry. Then look no further as a leading Pharmaceutical company are looking for a CSV Remediation Engineer You will join the PQS Global team that will be allocated to the remediation of identified gaps. This is a 12 month contract working on a very exciting project with the possibility of an extension. In this role, you will be responsible for but not limited to:

• Ensure compliance with regulatory bodies for GMP pharmaceutical regulatory agencies.
• Collaborate with iQMS and other various teams to review and approve documentation.
• Work in conjunction with Global IT teams and cross-functional teams to identify, create, review, and approve documentation.
• Assist in locating, organising, and approving the resources needed to create, evaluate, and approve IT infrastructure documentation.

• 3 + years' experience working with validation and qualification projects within GMP regulated environments.
• Experience in the pharmaceutical industry.
• Hands-On knowledge & understanding of CSV requirements for all aspects of computer systems and infrastructure involved in medicinal product production.
• Excellent interpersonal, communication (written and verbal) and time-management skills.
• Detail-oriented with a commitment to maintaining the highest standards of compliance.

• Consultant | Life Sciences & Engineering Recruitment
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