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CSL Behring

  • United States

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. We meet patients’ needs to develop and deliver innovative therapies that are used to treat coagulation disorders, primary immune deficiencies, hereditary angioedema, respiratory disease, and neurological disorders. CSL Behring’s products are also used in cardiac surgery, burn treatment and to prevent hemolytic disease of the newborn.

The company operates one of the world’s largest plasma collection networks, CSL Plasma. The parent company, CSL Limited, headquartered in Melbourne, Australia, employs more than 27,000 people, and delivers its life-saving therapies to people across the globe.

We are looking for people who want to live their Promising FUTURES and fulfill their individual career aspirations at a purpose-driven company with a strong values-based culture.

We want CSL to reflect the world around us

Tackling some of the world's toughest health challenges requires a diverse approach to problem solving. As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. It’s the foundation of who we are. We believe that by harnessing and honoring the unique capabilities, experiences, and perspectives of our people, we are better able to serve our patients.

Join us! Together we’ll discover innovative solutions to better serve patients with rare diseases and protect public health around the world.

Jan 23, 2025
Full Time
Senior Regulatory Strategy Expert
CSL Behring Koto City, Tokyo, Japan
Responsibilities:• Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals it needs to conduct its current and future business activities; and produce, sell, and distribute its goods and services.Qualifications:• Bachelor, Advanced degree in a Life Science (PhD, MD) or Business (MBA) preferred.• 7+ years regulatory experience in the pharmaceutical industry. Biologics Regulatory experience preferred.Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.Our BenefitsWe 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 BehringCSL 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...
Jan 23, 2025
Full Time
Senior Director, Quality
CSL Behring Broadmeadows VIC 3047, Australia
CSL is undergoing extensive change as we expand and grow. In addition to contributing to Australia's export economy, CSL has invested and continues to invest in substantial new infrastructure to support CSL's global strategy and provide the network with crucial supply of product sourced from our Broadmeadows facility.As the Senior Director, Quality for Australia's largest pharmaceutical manufacturing site, you will be a key member of CSL Behring Australia's leadership group. Your leadership of the Quality function for CSL Behring Australia will support the growth trajectory of our successful Australian business.Your responsibilities will include:Ensure product and system complianceLiaise with the Therapeutic Goods Administration Laboratories, their GMP Compliance Branch and the relevant FDA departments to strengthen relationships in order to understand and anticipate legislative requirements or changes.Leadership of your team to ensure alignment of strategies, policies and...
Jan 23, 2025
Full Time
Medical Representative, Assistant Mgr
CSL Behring Koto City, Tokyo, Japan
Position Purpose: ・HZ/PGのブランドプラン・エリアセールスプランに則り、Highポテンシャルである脳神経内科・血液内科・小児科において、CIDP・SID・PIDに対する適正使用および症例獲得の最大化を目指す。・Ig BU Area Sales Managerと連携し、Ig BUのターゲット施設でのMRプランを策定し、実行する。Reporting Relationships: Reporting to Ig BU Area Sales ManagerMain Responsibilities and Accountabilities: ・Area Sales Plan作成にArea Teamのメンバーとして貢献する・ブランドプランに則り、自身のエリアの深い分析を行い、MRプランを立案し戦術を実行する・ブランドプラン、エリアプランに則り、ターゲットDrにCIDP、SID、PID（顧客・患者ごとに対して）の提案を実施する・顧客エンゲージメントを高めるためにC360 Veevaを使用して顧客分析および戦略を策定する・マルチチャネル(デジタルを含む)を顧客毎に効果的に活用し、情報提供を実施する・コンプライアンスを遵守し、適正使用情報を推進するPosition Qualifications and Experience Requirements: Education 学士卒以上Experience・主要な大学病院を担当し、MRとして重要なKOLを担当した経験を持つCompetencies・ブランドプランを理解し、実行することが出来る・効果的な施設プランを策定し、実施することが出来る・KOLに対し、物おじすることなく、治療提案が出来る・常に最新の医学情報を仕入れ、自己学習を怠らない・常にCSL Valuesを意識し行動している・デジタルリテラシーがあること・セルフスターターであること・Wining mindset、Selling skilを持つ・（可能であれば）脳神経内科、血液内科、小児科領域の経験を持つOur Value: Patient Focus, Innovation, Integrity, Collaboration, Superior Performance.Our BenefitsWe encourage you to make...
Jan 22, 2025
Full Time
Head of Execution Systems - APAC
CSL Behring Broadmeadows VIC 3047, Australia
Your RoleThe Head of Execution Systems - APAC is responsible for overseeing the Manufacturing Operational Technology (OT) applications, systems, and software used to support the production of commercial materials.  This includes direct oversight of the Manufacturing systems including but not limited to Manufacturing Execution Systems (MES), and Distributed or Process Control Systems (DCS/PCS). You will also provide strategic direction to the APAC teams responsible for the design/development, implementation, and operational support of manufacturing execution philosophy and associated standards for batch processing activities.  Your Responsibilities Reporting to the Global Execution Systems Head you will:Lead/provide the strategy for implementation, improvement, qualification, lifecycle and sustainability of APAC region Manufacturing Execution SystemsBe responsible for leading a regional group accountable for the development, implementation (Opex & Capex) and operational support...
Jan 22, 2025
Full Time
Key Account Executive / Manager (Two years contract), CSL Malaysia
CSL Behring
Are you ready to make a meaningful impact in the biotechnology field? Join us where you’ll play a key role in bringing life-changing therapies to those who need them most.Your mission will be to maximise budget results in Southern Malaysia. You will manage existing sales while seeking out new opportunities, always aligning your efforts with our strategic goals across various Therapeutic Areas.We are counting on you to drive the success of our products, achieving both qualitative and quantitative objectives set in collaboration with your Line Manager. As a vital bridge between CSL Behring and our valued customers, you will help project our company as a trusted leader in biotechnology.This opportunity is for a full-time, Contract employee under the payroll of a local pharmaceutical partner for 2 yearsJob Title: Key Account Executive / ManagerLocation: Southern (Malacca/ JB)Position Type: Full-TimeResponsibilities:Key Account Management:Develop and maintain strong relationships with...
Jan 22, 2025
Full Time
Head of Finance, FBP, Japan
CSL Behring Koto City, Tokyo, Japan
Position Purpose:The Affiliate Head of Finance is responsible for overseeing all financial operations, strategy, and governance for the affiliate, ensuring alignment with corporate objectives and compliance with local regulations. The role supports decision-making delivering insights on growth strategies, opportunities and risks, fosters strong partnership with cross-functional leaders, and drives financial discipline. The role has fiduciary responsibility for accounting, tax, and treasury, ensuring accurate financial reporting, efficient cash management, and adherence to tax obligations.Serving as a trusted business partner to affiliate and regional leadership, the Affiliate Head of Finance ensures precision in financial planning, reporting, and analysis while offering insights on growth strategies, opportunities and risks. driving operational efficiency and contributing to the company’s long-term success.The Head of Finance / FBP is responsible for delivering strategic finance...
Jan 20, 2025
Full Time
PV Manager
CSL Behring Shanghai, China
Responsibilities:• Ensures compliance with standard operating procedures, regulatory safety and pharmacovigilance in compliance with national and international regulations, such as the Food and Drug Administration (FDA), MHRA, PEI, EMA, PMDA, World Health Organization, country and regional regulations for the reporting of adverse events to regulatory agencies.• Develops and implements pharmacovigilance guidelines and ensures the uniform and timely processing of adverse event data on all marketed products in development.• Acts as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements.• Develops and prepares reports for company management as well as external regulatory agencies.• May provide medical evaluation of adverse event reports.• Assists in the preparation of new drug application safety updates, investigational new drug safety reports, investigator communications, product labeling/package inserts and...