Validation Associate, Facilities and Operations

The Validation Associate is responsible for supporting validation activities associated with pharmaceutical manufacturing equipment, utilities, computerized systems, facilities, and processes. This position crucial role in maintaining, scheduling, and executing qualification and validation activities for the manufacturing of tablets, capsules and spray drying dispersion for the use of clinical FDA trials. The successful candidate will support all facets of the validation life cycle including design, operation, continuous improvement, and decommissioning. Preference will be given to candidates with pharmaceutical industry experience within a GMP environment to best inform decisions and provide direction for the assurance of product quality.