| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| London Jobs |
| Manchester Jobs |
| Liverpool Jobs |
| Nottingham Jobs |
| Birmingham Jobs |
| Cambridge Jobs |
| Glasgow Jobs |
| Bristol Jobs |
| Wales Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | Stoke-on-Trent |
| Education | Not Mentioned |
| Salary | Competitive salary |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent , full-time |
Validation LeadFancy taking full validation ownership of an expanding site for a global biopharmaceutical companyBeing responsible for a small team with high potential, you will have the opportunity to work in a culture that offers true autonomy in order move objectives forwards. As this site has continued expansion of its manufacturing and laboratory facilities overrecent years, you will have a genuine scope for career development and be able to directly influence the validation strategy moving forwards.Despite the fact that this is a global business, this specific site has a long and successful history and culturally still feels like a family business, so you get to experience the benefit of both worlds.Given the scope of the opportunity your experience will be crucial across all areas of validation including equipment, process, cleaning and computer systems/CSV. Despite the size of the company, you need to enjoy working in a hands-on capacity and seeingthe results of your work.There will also be some flexibility for hybrid working.Experience: Degree level qualification in scientific subject Pharmaceutical / Biopharmaceutical validation experience across equipment, cleaning, process and CSV (dont worry, you dont need all of them!) Understanding of quality systems (i.e. CAPA, deviations, change control etc.) Any previous line management or supervisory experience would be valuableKeywordsValidation, IQ, OQ, PQ, equipment, process, CSV, computer, systems, quality, assurance, QA, CAPA, deviation, change, controlHarris Lord is acting as a recruitment agency for this role
Keyskills :
ManagementManufacturingPharmaceuticalSupervisory ExperienceValidation