CSV Lead – London – Competitive Package

I am working closely with a biopharmaceutical company who are actively looking to onboard a CSV Lead. This will be on an initial 12-month FTC, with the potential to be onboarded on a permanent basis after this period.

You will be responsible for:

• Line management of 1 QA/CSV Associate.
• Ensuring CSV systems are implemented and maintained to high quality standards.
• Supporting with QMS activities as and when required.
• Providing support regarding data integrity requirements.

You will bring the following:

• Broad and proven experience working across a GxP setting with particular focus on computer system validation and IT Compliance.
• Good working knowledge of GMP and MHRA regulatory guidelines.
• Line management background or skills would be advantageous.

If this role is for you or someone that you know then then please get in touch by reaching out to me on: dixie.rowley@biotalent.com