• A Bachelor’s degree (BS or BA) in Chemistry or related technical/physical science from an accredited college/university is required. A master’s degree in a field of study relevant to the position is preferred.
• Not less than (NLT) five (5) years of relevant experience in QA auditing across GMP functions.
• Experience working in Rx pharmaceutical manufacturing environments is preferred.
• Preference will be given to candidates with ASQ certification(s) in areas related to Pharmaceutical auditing, vendor auditing, self-inspection, etc. and candidates that are Six-sigma certified.
• Solid project management skills and experience is required.
• NLT five (5) years relevant experience directing work in a group setting.
• Proficiently speak English as a first or second language.
• Proficiently communicate and understand (read and write) scientific / regulatory based ‘work” in English.
• Bi-lingual in the Spanish language (speaking, writing, interoperating and translation) is preferred.
• Have excellent organization, learning and teaching skills required to work in teams.
• Ability to understand and analyze complex data sets.
• Know how to use Microsoft Office programs and other scientific based software.