Document Control Specialist- GMP or pharmaceutical - (Lancaster, SC)

POSITION DETAILS: The position will provide assistance with maintaining GMP documentation system. ROLES AND RESPONSIBILITIES * Assist in implementing details systems for managing document tracking, controlled document distribution (issuance) and records management. * Oversee the issuance and maintenance of logbooks. * Facilitate the final review of production batch records. * Assist in administering the change control system (issuance, tracking, and implementation). * Consult with other QA and site personnel to ensure timely issuance and execution of records in the quality systems. * Maintain accurate records for the location of records generated by quality systems. * Follow all applicable SOPs, policies and other guiding documents that describe document life cycle management. THIS POSITION WILL BE CLOSELY ASSOCIATED AND WORK WITH THE FOLLOWING * * Operation Management and Personnel * Quality Assurance Management