Thermo Fisher Scientific seeks a Lead Document Control Administrator to oversee daily document management activities, maintain compliance and regulatory standards, and serve as the subject matter expert for document control processes and electronic systems. The role includes mentoring team members and collaborating across departments.
Responsibilities
Coordinate daily document control activities and oversee document lifecycle management
Maintain document accuracy, version control, audit trails, and regulatory compliance
Provide technical guidance to end users and mentor team members on EDMS and procedures
Support internal, customer, and regulatory audits; participate in change control and CAPA initiatives
Generate performance reports and recommend process improvements for document control operations
Requirements
Bachelor's degree in Business Administration, Life Sciences, Engineering, Quality, or related field
3+ years of document control or quality systems experience in regulated industry
Hands-on experience with Electronic Document Management Systems (EDMS)
Knowledge of FDA 21 CFR Part 11 and 21 CFR Part 820 regulations
Thermo Fisher Scientific seeks a Lead Document Control Administrator to oversee daily document management activities, maintain compliance and regulatory standards, and serve as the subject matter expert for document control processes and electronic systems. The role includes mentoring team members and collaborating across ...
... Control Administrator is responsible for coordinating and overseeing daily document control activities to ensure the accuracy, integrity, and compliance of controlled documentation. This role serves as the subject matter expert (SME) for document control processes and electronic document management systems (EDMS), provides ...
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