Documentation Specialist

Overview In this contract role, you will support quality and regulatory processes by tracking and reviewing change control documentation and assisting with editing quality documents to ensure regulator compliance. You will work in a fast-paced environment requiring accuracy and effective collaboration across teams. The position emphasizes strengthening document quality, SOPs, and validation master plans while leveraging your attention to detail and problem-solving skills. This is a hands-on opportunity to contribute to compliant, well-documented quality systems in a pharmaceutical setting. ResponsibilitiesTracking and reviewing change control documentationAssisting with editing quality documents (SOPs, guidelines, validation master plans) for regulator compliance Key requirements3 to 6 years experienceProficient in Microsoft Office applications/word processingAdobe Acrobat, formattingSME level understanding of functional area electronic business systemsCritical thinking to develop strategies and improve practicesProfessional business communication skills (peer to peer and upward)peer to peer communicationupward communicationteam collaborationMicrosoft OfficeAdobe Acrobatelectronic business systems