CSL Behring has an exciting prospect for Manufacturing Assistant to join our dynamic team within the Manufacturing function (Base Fractionation – Facility F).
Based at Broadmeadows and reporting to the Facility F Supervisor, you will support the execution of daily manufacturing process operations in a protected, GMP-compliant, and cost-efficient manner.You will contribute to routine manufacturing activities by applying your knowledge of processes, procedures, and equipment to ensure the weekly manufacturing schedule is achieved.
The role focuses on hands-on operations involving live process and product while maintaining strict adherence to established methods of manufacture (BMPs) and regulatory standards.Multiple roles are available as 12-month fixed-term opportunities.Shift Details:11-hour rotating shifts between day (5am or 7am starts) and night (5pm or 7pm starts), working a rotating roster of three days on / three days off.The RoleReporting to the Facility F Supervisor, your responsibilities will include:Execute routine manufacturing activities in accordance with SOPs and standard work instructionsEnsure all activities are performed in compliance with cGMP, regulatory requirements, and CSL policiesSupport safe, efficient, and compliant operation of the Facility F manufacturing environmentPerform routine process tasks including:Plasma intermediate handling and transportEquipment and solution preparationClean-in-place (CIP)
supportBuffer preparation (weighing and dispensing materials)Facility cleaning and housekeepingOperation, assembly, disassembly, cleaning, and basic maintenance of equipmentMonitor and meet the weekly manufacturing schedule, escalating risks to delivery promptlyComplete documentation accurately and in a timely manner to support product quality and complianceMaintain stock levels of consumables and cleanroom garments within the manufacturing areaContribute to continuous improvement initiatives to enhance safety, quality, compliance, and efficiencySupport investigation activities as a subject matter contributor where requiredAssist in preparation for regulatory inspections (e.g. TGA, FDA)Work collaboratively with internal stakeholders to ensure manufacturing targets are achievedTo Be SuccessfulStrong attention to detail with the ability to follow documented processes preciselyExperience working in a structured, process-driven manufacturing environment (pharmaceutical, FMCG, food or similar preferred)A proactive team player with good communication and problem-solving skillsDemonstrated ability to work safely with a strong focus on quality and complianceAbility to manage routine operational tasks to meet schedule requirementsFlexibility to work rotating shifts aligned to manufacturing operationsStrong written and verbal communication skillsAlignment with CSL values and behavioursPlease submit your application (cover letter and resume) in one document.
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