Validation Manager

Validation Manager  - Contract - North East

Quanta are thrilled to be working with a world leading cGMP Contract Development and Manufacturing Organization (CDMO). 

Supporting their partners in the biopharmaceutical industry with the development and production of their therapeutic candidates. Their mission is to help their customers bring their biologic and vaccine candidates to the clinic and, ultimately, to commercialisation.

They are licensed for the commercial manufacturing of six approved products and due to continued growth, they are looking for a Validation Manager in the UK. 

The UK site is under a large scale CAPEX investment programme covering a mixture of manufacturing facility upgrade and expansion as well as the construction of new office facilities.

Role:

To support this significant investment project, the need for a seasoned Validation Project Manager has been identified – they will be involved in developing and delivery of the validation programme by working in conjunction with departmental heads such as QC and QA.

Skills/Experience: 

• Degree Qualified
• Experience working within a biopharmaceutical or pharmaceutical manufacturing organisation
• Proven backgrounds in managing a team of validation engineers
• Strong validation lifecycle experience to include: URS/Protocol Generation etc..
• Strong project management experience
• Stakeholder management experience

The candidate must have the rights to work in the location stated in the job advert.

Please note, Quanta Consultancy Services does not sponsor Visa applications.

To view Quanta's privacy policy, please visit our website