GMP QA Document Controller & Compliance Coordinator

The Role & What You Will Be Doing

• Work with the Quality systems owner to coordinate, review, and manage the site control of GMP documents.
• Perform a detailed review of document changes prior to final approval.
• Manage the distribution of new documents and or retrieval of old documents (internally & externally).
• Coordinate the archiving of quality records.
• Assist in the preparation, revision and review of quality system records.
• Assist in the maintenance and delivery of quality related training applicable to your job role.
• Assist in the management of the incident report, CAPA, change control and Customer Complaints systems as required.
• Prepare weekly/monthly/quarterly/annual KPI/Management review data as required.
• Perform other duties as assigned.

Minimum qualifications for this role are:

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

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.