20,265 Jobs in Melbourne

Your Opportunity

At CSL Behring, we are driven by our promise to save lives and protect the health of people around the world. As a global biotechnology leader, we deliver innovative therapies that help people with rare and serious diseases live full lives.

We are currently recruiting for a Lifecycle Project Coordinator to join our Lifecycle Management team at Broadmeadows site on a 2-year fixed term contract .

Reporting to the Head of Lifecycle Management , you will manage product introductions, discontinuations, and packaging projects. This role is pivotal in ensuring that printed packaging materials meet regulatory, quality, customer, and manufacturing standards. You will collaborate across global and local teams including Regulatory, Quality, Procurement, Planning, Production, Logistics, and Engineering, to deliver compliant, timely, and cost-effective outcomes.

Your Role

• Manage New Product Introductions (NPIs) and End-of-Lifecycle (De-Launch) processes

• Oversee printed packaging materials (cartons, labels, leaflets) throughout their lifecycle

• Act as SME for printed materials during audits and investigations

• Drive continuous improvement and contribute to global initiatives

• Support vendor changes and resolve supply chain issues

• Coach and mentor Lifecycle Associates

Your Skills & Experience

• Tertiary qualification in business or relevant discipline

• Strong project management and organisational skills

• Experience in pharmaceutical or regulated environment (preferred)

• Excellent interpersonal and stakeholder engagement abilities

• Knowledge of GMP, change control systems, and regulatory labelling requirements (highly desirable)

How to Apply

Please submit your application including your resume in one document.

Apply now to join a team that’s making real change in the lives of patients worldwide.

#LI-Onsite

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL.

The Opportunity

Join a dynamic and collaborative finance team as an Accounts Receivable Analyst at CSL. Reporting to the Accounts Receivable Manager, you'll help manage the full AR process in a small, agile team. This is a unique opportunity to take ownership of end-to-end AR responsibilities while working closely with company stakeholders across Sales, Customer Service, and Business Partners.

The Role

• You will manage end-to-end accounts receivable processes including collections, cash applications, and credit management.

• You will investigate and resolve

Your Role

CSL are hiring a Senior Automation Engineer (internally referred to as the Senior Value Steam Recipe Owner) to manage the implementation, maintenance and ownership of PCS/MES and PLC process recipes.

This role will also include coordinating the definition of the required hardware with the Platform Owner, including the development of the software, and system coordination, to enable Commissioning and Validation of the Process Systems.

This position is offered as a 2 year contract.

Your Responsibilities

Reporting to the Execution Systems Lead you will:

• Be the Technical subject matter expert including oversight & review of contractors/integrators work during design, construction, commissioning, and validation
• Ensure the overall recipe design and implementation meets Engineering and Manufacturing requirements for the operation of the plant
• Ensure installation and configuration to the ISA-S88/S95 standard during the following Project phases: Requirements definition, detailed design generation, software configuration, system integration and Qualification testing
• Participate in the creation of the Execution System validation strategy together with the Global and Site CSV & Quality representatives and ensure strong contribution to audit inspection
• Perform the Project Manager Role on an interim basis. Ensuring that project work is completed within budget and on schedule

Your Experience

• Bachelor of Science in an Engineering or other relevant Science discipline i.e. Computer Science or Management Information Systems
• At least 5 years' practical experience in pharmaceutical industry including direct management experience in Manufacturing, Engineering or Execution Systems/Automation
• Specific experience in process automation, MES and batch manufacturing industry standards (ISA S88 &S95)
• Hands on experience in Recipe and Workflow Authoring, configuring master data and equipment in MES would be an advantage
• Direct experience designing, building, deploying and supporting automation and execution systems in a process-based manufacturing environment

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL.

Your Role

CSL are hiring a Senior Automation Engineer (internally referred to as the Senior Value Stream Platform Owner) to manage the technical installation & setup,

The Position:

The R&D Advanced Analytics, Automation, and AI Lead is responsible for executing the R&D digital acceleration roadmap, with a primary focus on delivering business value through advanced and emerging technologies. In close collaboration with I&T, this role oversees the design, development, and deployment of analytics, automation, and AI/ML solutions across the R&D value chain. The leader partners with RDLT, TES LT, I&T, and external innovation ecosystems to identify and apply disruptive technologies that enable measurable transformation. Acting as a strategic bridge between R&D and I&T, this role ensures digital acceleration initiatives are technically robust, operationally impactful, and fully aligned with enterprise architecture and capabilities.

Responsibilities:

• Lead the development and execution of the R&D digital acceleration roadmap focused on automation, AI, and advanced analytics
• Identify disruptive technologies and use cases (e.g., generative AI, intelligent automation, simulation, digital twins)
• Partner with business stakeholders to develop scalable, production-ready digital solutions
• Lead agile teams to develop models, tools, and platforms aligned with R&D needs
• Drive rapid experimentation and innovation, ensuring feasibility, compliance, and user adoption
• Establish metrics to measure the impact of digital interventions on cycle times, quality, and outcomes
• Oversee partnerships with AI/ML vendors, academic collaborators, and industry consortia
• Build internal capabilities and talent pipelines for digital and analytics functions
• Ensure that all AI, automation, and advanced analytics solutions are implemented in a compliant manner, supporting readiness for regulatory audits and inspections involving emerging technologies
• Provide thought leadership in AI, including the development and implementation of AI governance frameworks, ethical AI practices, and active engagement with industry consortia such as Pistoia Alliance, CIOMS, TransCelerate, and other relevant forums to shape standards and best practices

Education & Requirements:

• Master’s or PhD in Data Science, Engineering, Computer Science, or related fields
• 15+ years of experience in digital leadership or advanced analytics/AI roles within R&D-driven pharmaceutical industry
• Deep knowledge of life sciences and experience applying AI/ML and automation in scientific or regulatory domains
• Demonstrated ability to deliver AI-enabled tools in regulated environments
• Strong cross-functional collaboration and change leadership skills
• Expertise in digital product lifecycle, from experimentation to scale
• Experience supporting regulatory audits and inspections involving emerging technologies, including AI and automation, in a GxP or highly regulated environment

CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL has many benefits to help achieve your goals.

Please take the time to review our benefits site to see what’s available to you as a CSL employee.

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL.

The Opportunity

CSL Behring is seeking a Senior Associate, Quality Assurance Compliance to join our Quality team at Broadmeadows on a fixed-term contract (approximately 13 months). Reporting to the Manager, QA Compliance , you’ll play a key role in maintaining audit readiness and supporting compliance across the site. You’ll work closely with a small, collaborative team and engage with multiple departments across the business.

Your Role

• Support the Self-Inspection Program , including scheduling, conducting audits, and managing CAPAs.

• Prepare for and participate in Regulatory Authority and Internal Audits , including TGA and FDA inspections.

• Ensure audit findings are addressed and closed out in alignment with regulatory expectations.

• Maintain and update documentation in electronic quality systems (e.g., TrackWise, Veeva).

• Collaborate with cross-functional teams to ensure compliance with global regulatory standards.

• Support the Quality Management System and contribute to continuous improvement initiatives.

Your Skills and Experience

• Bachelor’s degree in Science, Engineering, or a related discipline.

• 3–5 years’ experience in pharmaceutical manufacturing or a highly regulated industry.

• Experience conducting audits or supporting regulatory inspections.

• Familiarity with GMP and regulatory frameworks (e.g., FDA, TGA, EMA).

• Preferred familiarity in electronic quality systems such as TrackWise, Veeva, or similar.

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL.

Your Role

CSL Seqirus are hiring multiple Instrumentation Technicians at our new state of the art site in Tullamarine, Melbourne. This world class 28,400 square metre facility includes clean-rooms, office and manufacturing space to support the production of influenza vaccines and critical antivenoms for Australia and other markets.

You will manage fault correction, calibration, preventative maintenance, and overhaul of instrumentation and control equipment.

Initially you will be employed under a 10-day fortnight to take part in the commissioning of the facility on day shift then transitioning to a rotating 12hr shift pattern including both day and night shifts to support production.

Your Responsibilities

Reporting into the Electrical Engineer – Electrical & Instrumentation you will:

• Shut down, isolate and test run machines and equipment as required for maintenance purposes

• Diagnose faults in, repair and calibrate control and monitoring loop elements, electronic systems and sub-assemblies

• Diagnose faults on interconnected and non-interconnected electrical circuits and systems

• Perform routine calibration of process instruments, both in-situ and in the workshop

• Perform preventive maintenance tasks

• Interpret control system and electrical/electronic circuit diagrams and engineering drawings and prepare sketches of system and circuits/circuit modifications

• Maintain workshop equipment and any reference calibration instruments in a state to be used in a GMP environment

• Other tasks include assisting in maintaining the integrity of the SAP Computerized Maintenance Management System (CMMS), engineering stores and perform tasks including work planning (scope, setup, isolation, and risk assessments), scheduled servicing, breakdowns, shutdowns, commissioning, and test running machines and equipment

Your Experience

• Relevant Trade Qualification (Cert III-Cert IV or equivalent) as an Electrical OR Instrumentation technician

• Experience across a wide range of technical instrumentation in a pharmaceutical, FMCG, oil and gas or similar industry

• Sound understanding of calibration methods and experience in conducting non-conformance investigations

• Computer literacy – knowledge of SAP or another CMMS system

• A commitment to the safety of yourself and your team

• Fault-finding and problem-solving skills

CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus.

CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

We want CSL Seqirus to reflect the world around us

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL.

Watch our ‘On the Front Line’ video to learn more about CSL Seqirus

The Opportunity

Join CSL’s Site Exit Engineering team as a Project Engineer – Decommissioning on a fixed-term contract. You’ll be part of a small, focused team of three, reporting to the Site Exit Engineering Lead, working alongside another Project Engineer. This role supports the decommissioning of CSL’s historic Parkville site as operations transition to Tullamarine and Elizabeth Street.

The Role

• Execute decommissioning activities for equipment, utilities, systems, and facilities in a compliant and structured manner.

• Prepare and manage detailed decommissioning documentation aligned with GMP standards.

• Support medium to large-scale projects, including planning and coordination of plant shutdowns.

• Raise and manage purchase orders for goods and services related to decommissioning.

• Assist in construction activities and ensure safety and compliance throughout project execution.

• Contribute to project management documentation and reporting.

Your Skills and Experience

• Bachelor’s degree in Engineering (Mechanical, Electrical, or related field).

• 3–5 years’ experience in a regulated manufacturing environment (pharmaceutical, food & beverage, etc.).

• Hands-on experience with commissioning or decommissioning of equipment and systems.

• Familiarity with GMP documentation processes and systems such as Veeva or TrackWise.

• Understanding of cGMP, EHS, and Quality Management Systems.

CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus.

CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

We want CSL Seqirus to reflect the world around us

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL.

Watch our ‘On the Front Line’ video to learn more about CSL Seqirus

Your Role

Join CSL Behring , a global leader in plasma-derived therapies, as an Engineering Data Support specialist. In this critical role, you’ll be the custodian of engineering master data in SAP, supporting preventive maintenance, calibration, and materials management across our manufacturing site.

You’ll work closely with engineering, validation, and production teams to ensure data integrity, regulatory compliance, and operational efficiency.

Your Responsibilities

• Manage and maintain engineering master data in SAP (Assets, PM schedules, Calibration, Materials).

• Perform data cleansing, transformation, and uploads using tools like LSMW.

• Respond to service requests and troubleshoot system issues.

• Conduct system testing and support upgrades or fixes.

• Generate reports and dashboards using Excel and Power BI to support decision-making.

• Deliver training to new users and support continuous improvement.

• Ensure data quality and compliance with GMP and regulatory standards (TGA, FDA, EMEA).

Your Experience

• Tertiary qualification in Engineering or Science, or 3+ years in a similar technical role.

• 2–5 years’ experience in engineering data, maintenance systems, or pharmaceutical manufacturing.

• Strong SAP experience (S/4HANA preferred); LSMW desirable.

• Advanced Excel and familiarity with Power BI, Tableau, or QlikSense.

• Understanding of GMP/cGMP and quality systems in regulated environments.

• Excellent attention to detail, problem-solving, and stakeholder communication.

Why Join Us?

• Be part of a purpose-driven team saving lives through innovation.

• Enjoy flexible work arrangements and a collaborative culture.

• Work with cutting-edge systems and contribute to high-impact projects.

Apply now to join Australia's largest pharmaceutical manufacturer. Our passion is to save lives and protect health in people everywhere. At the core of our DNA is a resolve to always be innovating for our patients!

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Learn more Inclusion and Belonging | CSL.