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