For our Biopharmaceutical Product Development (BPD) division, we are looking for a

Associate Director/ Head of Analytical TT Strategy Recombinant (m/f/x)

R-248368

Fulltime / permanent/ non-tariff

The Head of Analytical TT Strategy (Recombinant) is responsible for supporting the Marburg and Melbourne BPD Recombinant early and late clinical phase Portfolio. Working with key BPD stakeholders, this role will refine and manage the BPD Recombinant Analytical outsourcing and TT Strategy. The role reports to the Director, Analytical Tech Transfer Strategy & Technical Project Management.

The Opportunity

Key point of contact and Management of strategic partners for Contract Analytical Services including forecasting, reporting and oversight of budgets.Management of Biopharmaceutical Pharmaceutical Product Development (BPD, Recombinant) Analytical Outsourcing and Tech Transfer Strategy Executing Analytical strategic plans for BPD projects (Recombinants).Leading Tech Transfer of BPD analytical activities projects internally and externallyEnsuring project requirements, both internal and external stakeholders are met with respect to quality, cost and timelines. Participate in due diligence activities for New Product OpportunitiesUtilise insights from the product development pathway and global biopharmaceutical trends to guide R&D policy, support preparation of regulator packages and identify new opportunities for cost savings and process efficiencies.

Your Skills and Experience

Post graduate qualification in a relevant branch of Chemistry or Biological ScienceAt least 10 years hands-on experience in Analytical Development and related process development activities.Understanding of and experience in the production and technology transfer of protein therapeutics including, chromatographic separation/fractionation of proteins and other methods of protein purification, formulation activities and associated analytics (in-process, characterization and GMP release methods), from bench-scale to clinical manufacturing scaleUnderstanding of the regulatory requirements and compliance standards (FDA, EMA, JP, TGA) associated with GMP production of proteins for clinical development programs, process validation & characterisation required for BLA applications.

What we offer

Excellent income potential and extended benefits Up to two additional leave days for your personal wellbeingFamily services such as psychological support, legal advice, family care services and more for you and your direct familyHybrid working models

For more information, please check out our global benefits below

We are looking forward to your application. Please ensure to apply online with your, cover letter, CV and certifications as well as your salary expectation.

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!