Document Lead/Manager

Summary: The Document Lead/Manager oversees the control, organization, and lifecycle of project documentation to ensure compliance with regulatory standards and internal procedures in the pharmaceutical environment.

Responsibilities

Develop, implement, and maintain document control systems and procedures.Manage the creation, review, approval, revision, and archiving of all project documents.Ensure timely distribution and accessibility of controlled documents to authorized personnel.Train team members on document management processes and regulatory requirements.Audit document control practices to identify and address gaps or compliance issues.Experience:Bachelor’s degree in Life Sciences, Information Management, or related field.7+ years’ experience in document control or management, preferably in the pharmaceutical or regulated industry.Proficient with electronic document management systems (EDMS).Strong organizational, communication, and auditing skills.