With operations in 35+ nations and ~ 27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma , one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

The Opportunity:

We currently have an exciting permanent full time opportunity for an experienced R&D Quality Associate to join our team in Parkville. In this position, you will perform QA review of batch documentation for R&D pre-clinical and clinical product batch release to meet the R&D product release timelines for use in clinical studies sponsored by CSL or collaborators. Collation and distribution of Quality data to support Quality Management Reviews.

Duties Include:

• Review of R&D batch release documentation
  
• Conduct visual examination of non GMP products
  
• Support the QA team through collation and distribution of compliance data
  
• Liaison with R&D departments regarding quality related issues
  
• Update of QA Documents
  
• Support R&D Quality system updates
  
  

Skills and Experience

• Relevant tertiary qualification is desirable, with at least 1-2 years' experience in either manufacturing under GMP, quality assurance or process development.
  
• Understanding of GMP requirements in the pharmaceutical industry
  
• Working knowledge of Australian codes of GxP's
  
• Good interpersonal, negotiation and influencing skills
  
• Strong customer service focus
  
• Ability to work well independently and to self-motivate
  
• Well-developed organisational and time management skills
  
• PC skills (Microsoft Office)
  
• Strong oral and written communication skills
  
• Team orientated
  
  

How to Apply:

Applications must address the selection criteria above and include a current CV and covering letter.

Worker Type:
Employee

Worker Sub Type:
Regular