Senior Associate, Operational Services Bulk
The Opportunity
CSL Behring is seeking a Senior Associate, Operational Services to join our dynamic team at the Broadmeadows facility. Reporting to the Senior Manager or Manager, Operational Services, you'll play a key role in managing deviation investigations and supporting change initiatives within the Bulk Manufacturing area. You'll be part of a collaborative and high-performing team that values diverse technical backgrounds and proactive problem-solving.
Workplace Flexibility: This is primarily an on-site role, (approx. 80%), based in Broadmeadows, with flexibility for occasional work-from-home days. Standard hours are also flexible.
Your Role
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Lead end-to-end investigations of deviations in the Bulk Manufacturing area, including root cause analysis, CAPA definition, and documentation suitable for audit presentation.
-
Coordinate and implement routine changes to manufacturing processes, ensuring alignment with operational goals and compliance standards.
-
Act as change coordinator for GxP-related changes and represent the manufacturing value stream in cross-functional project teams.
-
Manage timelines for deviation closures (within 30 days) and escalate issues to ensure timely resolution.
-
Collaborate with stakeholders across manufacturing, QA, and engineering to drive effective outcomes.
-
Maintain expertise in deviation management, change control, and root cause analysis through continuous learning and application.
Your experience
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5–10 years of experience in pharmaceutical, biotechnology, or biological manufacturing, R&D, Technical Services, or Quality.
-
Tertiary qualifications in Science or Engineering.
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Demonstrated experience managing deviations, including investigation leadership and CAPA development.
-
Familiarity with cGMP, regulatory requirements, and audit preparedness in a manufacturing environment.
-
Experience with change management processes and tools in a GxP setting.
Our Benefits
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.
About CSL Behring
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.
We want CSL to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.
Do work that matters at CSL Behring!
The Opportunity
CSL Behring is seeking a Senior Associate, Operational Services to join our dynamic team at the Broadmeadows facility. Reporting to the Senior Manager or Manager, Operational Services, you'll play a key role in managing deviation investigations and supporting change initiatives within the Bulk Manufacturing area. You'll be part of a collaborative and high-performing team that values diverse technical backgrounds and proactive problem-solving.
Workplace Flexibility: This is primarily an on-site role, (approx. 80%), based in Broadmeadows, with flexibility for occasional work-from-home days. Standard hours are also flexible.
Your Role
-
Lead end-to-end investigations of deviations in the Bulk Manufacturing area, including root cause analysis, CAPA definition, and documentation suitable for audit presentation.
-
Coordinate and implement routine changes to manufacturing processes, ensuring alignment with operational goals and compliance standards.
-
Act as change coordinator for GxP-related changes and represent the manufacturing value stream in cross-functional project teams.
-
Manage timelines for deviation closures (within 30 days) and escalate issues to ensure timely resolution.
-
Collaborate with stakeholders across manufacturing, QA, and engineering to drive effective outcomes.
-
Maintain expertise in deviation management, change control, and root cause analysis through continuous learning and application.
Your experience
-
5–10 years of experience in pharmaceutical, biotechnology, or biological manufacturing, R&D, Technical Services, or Quality.
-
Tertiary qualifications in Science or Engineering.
-
Demonstrated experience managing deviations, including investigation leadership and CAPA development.
-
Familiarity with cGMP, regulatory requirements, and audit preparedness in a manufacturing environment.
-
Experience with change management processes and tools in a GxP setting.
Our Benefits
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.
About CSL Behring
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.
We want CSL to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.
Do work that matters at CSL Behring!
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