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.