Senior Manager Downstream BMF

CSL Behring
AU - broadmeadows
June 14, 2024

The Opportunity

An exciting opportunity has become available in our Biotechnology Manufacturing Facility (BMF) for a Senior Manufacturing Manager - Downstream.
Reporting to the Director - Biotechnology Manufacturing Facility and based at our Broadmeadows site, you will be a member of the management team and collaborate in the general management of the facility.
You will lead the Downstream Manufacturing operations in manufacturing CSL's clinical human therapeutic products.

The BMF facility uses mammalian cells and DNA technology to manufacture drugs that will be used to treat life-threatening diseases.
The facility works with Process Development, Quality, and other technical and business functions to ensure efficient and safe drug substance manufacturing processes to produce multiple recombinant proteins.

The Role

Manage production activities to ensure completion of operations following the project schedule and the global project production schedule.
Ensure that all production deviations are reported and participate in the evaluation of all deviations; plan, lead and execute activities relating to the investigation of critical deviations.
Contribute to validation projects and risk assessments for the processes, facility and equipment and develop risk management strategies.
Participate in various BMF project activities and partner with other functional groups involved in technical transfer of manufacturing processes to the BMF.
Recommend modifications to operational procedures to improve operational integrity, increase the facility capacity and capability, reduce operating and GMP risks and improve operating safety and success.

Your skills and experience

Tertiary qualifications in Biological Sciences, Biotechnology, or Chemical Process or Science Engineering.
5+ years of experience in relevant production and quality environments.
Significant experience in a relevant pharmaceutical production environment.
Demonstrated understanding of cGMP, regulatory requirements and relevant environmental, health and safety requirements in manufacturing areas.
Demonstrated ability to co-ordinate project activities and liaise across functional groups to meet project targets and objectives

Apply now for a role with a varied remit in an organisation that is going through considerable investment and change.

Applications close 5pm AEST on 1 July 2024.

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 diversity and inclusion.
Learn more about Diversity & Inclusion at CSL.

Do work that matters at CSL Behring!

Read the full job description and apply online on the recuiter's web-site

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