Opportunity Description
About the company/role:
- Well-established pharmaceutical company seeking a Documentation/Quality Specialist to join their team
- 6-month contract
- Onsite, full-time hours (Mon-Fri)
- Normal business hours
- Based in South Eastern suburbs
Duties, but not limited to:
- Develop and evaluate quality and system procedures to ensure reliability, usability and compliance
- Write procedural documentation such as SOPs, work instructions and forms
- Collaborate with internal teams across departments and liaise with SMEs to extract information
- Review batch release documentation
- Review/approval revalidation and requalification reports and documentation
- Administration and maintenance of Quality Management Systems
- Performing visual inspections on intermediate and finished products
- Assist in the preparation of summary protocols and batch release documentati...
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