1 month ago
Stoke Stoke-on-Trent Competitive Permanent
Fancy taking full validation ownership of an expanding site for a global biopharmaceutical company?
Being 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 over recent 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 seeing the results of your work.
There will also be some flexibility for hybrid working.
· Degree level qualification in scientific subject
· Pharmaceutical / Biopharmaceutical validation experience across equipment, cleaning, process and CSV (don’t worry, you don’t need all of them!)
· Understanding of quality systems (i.e. CAPA, deviations, change control etc.)
· Any previous line management or supervisory experience would be valuable
Validation, IQ, OQ, PQ, equipment, process, CSV, computer, systems, quality, assurance, QA, CAPA, deviation, change, control
Harris Lord is acting as a recruitment agency for this role