Quality Systems Specialist | Remote US
MSI Pharma is supporting CSL Plasma in the search for an experienced
Quality Systems Specialist
to join their Quality organisation on a 6-month contract.
This fully remote opportunity is ideal for a quality professional with strong experience in document control, change control and electronic quality management systems within pharmaceutical, biotech or medical device environments.
Responsibilities
Manage controlled documents through review and approval workflows
Coordinate document reviews with SMEs and process owners
Support change control activities within the eQMS
Track approvals, implementation activities and closure milestones
Maintain audit-ready documentation
Support governance meetings and action tracking
Ensure compliance with GMP and Good Documentation Practices
Requirements
5+ years in Quality Systems, Document Control or Change Control
Pharmaceutical, biotech or medical device experience
Strong Veeva Vault QualityDocs experience
Experience with TrackWise, MasterControl or SharePoint desirable
Knowledge of GMP, GDP and quality systems requirements
Excellent communication and organisational skills