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 793 994 or Maria Julienne on 0491 694 371. NB - Only shortlisted candidates will be contacted.
