Job Description
Validation Specialist – London – Competitive Package
I am currently supporting a forward thinking pharmaceutical organisation that operate within the Viral Vector space.
They are looking for a permanent Validation Specialist to join their function and support with all aspects of qualification and validation.
You will be responsible for:
1. Support the development and documentation of the businesses strategies for Equipment, Facility, and PPM to align with EU GMP and regulatory standards.
2. Review and adhere to all necessary SOPs and protocols related to equipment, processes, and systems.
3. Contribute input on validation and qualification methods, strategic priorities, and resource requirements for new projects or re-qualification needs during review cycles.
You will bring the following:
1. Worked a validation position in a pharmaceutical GMP environment.
2. Well versed in equipment validation practices.
3. Good understanding of GMP regulations and requirements.
4. Experience working within a BioPharma/ATMP background would be advantageous.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: dixie.rowley@biotalent.com
Mobile: 03333076496
I look forward to hearing from you!