Scott Collins is Director of Laboratory Operations and Compliance at QPharma, Inc.  He has over 25 years’ experience in the pharmaceutical and medical device industries in the areas of Validation, Quality Control, Quality Assurance, Auditing, Manufacturing and Project Management.  Scott has been involved with remediation efforts associated with 483s, Warning Letters and Consent Decrees, being responsible for the management of the projects and their deliverables.  He has validated and been responsible for validating laboratory and manufacturing equipment and systems, as well as developing Quality Systems.  For several years, Scott held the position of Adjunct Instructor at NJIT teaching Validation and Regulatory Compliance Issues in the Pharmaceutical Industry.