Manager, Global Document Management

About the role

This role will lead operational priorities where safety, quality, compliance, and execution discipline are central to success. You will collaborate with field leadership, support functions, and cross-functional stakeholders to improve accountability, service delivery, and operational consistency. The position offers the opportunity to influence operational scale, customer outcomes, and organizational performance within a life sciences environment.

Responsibilities

• Support the development and improvement of the Quality System
• Prepare for GxP inspections and respond to regulatory bodies
• Manage global, regional, and local Standard Operating Procedures (SOPs) and Working Practices (WPs)
• Collaborate with key stakeholders for policy revisions and compliance
• Act as project liaison and support project activities as assigned

Qualifications

• Degree in natural science or equivalent experience
• 4+ years in clinical/industry/Regulatory Authority experience related to Quality Management
• Advanced knowledge of regulations in Pharmacovigilance and Clinical Development
• Experience in Monitoring, Quality Assurance, or Good Clinical Practices
• Well-versed in MS Office and strong communication skills

Pay

$107,718 – $161,000 annually

Benefits

• Comprehensive medical, dental, and vision coverage
• Tuition reimbursement and student loan assistance
• Generous 401(k) match with flexible time off
• Paid holidays and paid leave programs
• Company-provided life and disability insurance