The Validation Technician is responsible for coordinating and collecting samples in support of cleaning trials, cleaning validations, and deviations. The incumbent will work with Operations and R&D to determine sampling requirements and timelines. The incumbent will also be responsible for coordinating support for swab events on second/third/weekend shifts. Additional responsibilities include leading swab training and participating/leading continuous improvement projects.
Strong demonstrated Analytical Skills
Experience in the interpretation and applications of FDA requirements and cGMP.
The incumbent must have demonstrated the ability to organize multiple tasks and changing priorities to meet deadlines.
Excellent oral and written communication skills and excellent interpersonal skills are essential.
One or more years of pharmaceutical experience, experience writing technical documents, and ability to perform statistical data analyses preferred.
Minimum of Associate’s degree in Science or related field, with industry experience and an understanding of FDA requirements and cGMP preferred.
Website : http://www.perrigo.com
Headquartered in Ireland, Perrigo Company plc is a leading global healthcare supplier that develops, manufactures and distributes over-the-counter (OTC) and generic prescription (Rx) pharmaceuticals, infant formulas, nutritional products, animal health, dietary supplements, active pharmaceutical ingredients (API), and medical diagnostic products and receives royalties from Multiple Sclerosis drug Tysabri®.