Quality Assurance Documentation Controller

Job Responsibilities

• Work with the Quality systems owner to coordinate, review, and manage the site control of GMP documents.
• Support batch documentation issuance and reconciliation for the manufacturing records.
• Perform a detailed review of document changes prior to final approval.
• Manage the distribution of new documents and/or retrieval of old documents, both internally and externally.
• Coordinate the archiving of quality records.
• Assist in the preparation, revision, and review of quality system records.
• Manage the My University curricula for the QA team and coordinate training with SMEs.
• Support the management of material master data.
• Collate and report performance metrics within the QA group.

Qualifications

• Minimum of a Bachelor's degree (or equivalent) in a science related discipline.
• Experience within a pharmaceutical or medical device company is desirable but not essential; a combination of experience and education will be considered.
• Excellent attention to detail, written and oral communication, and interpersonal skills.
• Ability to handle multiple tasks in a fast paced environment with strong organisational and time management skills.
• Experience with various IT systems and software packages, including a strong working knowledge of Microsoft Office (Word, Excel, PowerPoint, etc.).
• Experience with electronic document management systems is desirable but not essential.

Benefits

• Competitive salary and benefits package.
• Career progression opportunities.
• Work life balance initiatives.
• Bonus scheme.
• Health insurance.
• Pension.
• Diversity and inclusion initiatives.

Equal Opportunity Employer

Viatris is an Equal Opportunity Employer.