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...