About the Company:

Operating as a global pharmaceutical manufacturer with global sites worldwide, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace.

A contract opportunity has now arisen for a QC Support Specialist to support the QC Team ensuring all raw material authorisation documentation is completed for the QC facility.

About the Opportunity: 
  
Key Responsibilities include the following:-

• Review raw material authorisation/release backlog for urgent site operations.
• Route & approve chemical specification revisions in VEEVA to implement reduced testing.
• Raise approval forms for GLIMS software builds.
• Ensure completion raw material qualifications including approval of reports and close outs.
• Assist with OOS, change controls, deviations.

About You:

The successful candidate will have the following skills & experience: 

• Tertiary Qualifications in Science/Pharmaceuticals.
• Previous experience in QC in chemistry. 
• Understanding of Raw Material Specification Documentation.
• GLIMS & VEEVA software experience.
• Maintain quality records within quality environment. 
• Sound report writing skills with attention to detail.
• Able to work independently & quick learner.

Culture & Benefits:

This is an Excellent Contract Opportunity for QC Support Specialist to join global pharmaceutical for QC documentation work within raw material authorisation. 

This is a Contract position requiring a START ASAP. 

How To Apply:

Interested Applicants please CLICK on the LINK below.
  
For further confidential discussion please call Sue Campbell on 1300 793 *** or Maria Julienne on 0491 694 ***.

NB - Only shortlisted candidates will be contacted.
Additional information

• Global Pharmaceutical Manufacturer
• Excellent Contract Opportunity - Start ASAP
• Melbourne Metro - Northern Suburbs