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Quality Control Analyst

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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

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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

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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

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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

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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

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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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