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Quality Control Analyst


Work for CSL Parkville! 12 month assignment – ASAP start. $39ph + super Quality Control Analyst. Role involves animal handling – please apply if you have animal handling experience and knowledge of ethics and regulations regarding animal handling.

CSL Validation Associate


Validation Associate Working for world renowned Biopharma Company CSL 12 month temp assignment – potential to extend ASAP Start Must haves: * 3yrs experience in Validation (Not doing method validation) Looking for someone with experience in validation of QC Equipment – Not QC ops or production equipment * Able to resolve issues independently * Person must be a self starter and be able to solve problems * Engineering or Science degree with 3-4 years ideally in validation experience

Quality Compliance Business Partner


Quality Compliance Business Partner, 12 month Assignment with possible extension. CSL, Parkville. Must haves: – 5+ yrs experience in a similar role – Pharmaceutical experience and Pharma Industry background – Exposure to quality systems – Experience with quality management and quality systems – Experience with a manufacturing site

Regulatory Affairs Manager


Position Title: Regulatory Affairs Manager Number of Vacancies: 2 Start Date: ASAP (earliest November; latest 1 Jan) End Date: 6 months (extension possible) CSL – Melbourne CBD

QC Analytical Technology Scientists x 3


Currently recruiting 3 x QC Analytical Technology Scientists – 1 in Biochemistry, 1 in Chemistry and 1 in Microbiology for 12 month, full-time assignments with CSL Location: Broadmeadows.

Senior R&D QA Associate, Procedural Document Specialist


This position exists as a member of the Global R&D QA department assisting the R&D QA Quality Systems organization with management of the Document Management Systems (DMS) activities to support the R&D Quality Management System. The Senior R&D QA Associate will be responsible for the overall content and maintenance of the DMS system on behalf R&D Quality and will coordinate document management workflow activities for personnel supported by the R&D Quality Systems organisation.

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