APAC/LATAM Regulatory Affairs Hematology Lead
vor 1 Tag
CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.Main Responsibilities and Accountabilities: The position holder is accountable for driving and implementing Innovative Regional Regulatory TA Strategies for the APAC/ LATAM TA. Driving and executing comprehensive, commercially and globally aligned regional regulatory activities across APAC/ LATAM Region for the TA. Accountable for CSL relationship with HA in the Region.Drive empowerment and capability-building initiatives for the TA team of RRL's, fostering informed decision-making and strong regional ownership.Establish and enhance effective communication channels and knowledge-sharing frameworks across local and global stakeholders.Represent Global Regulatory in regional or global health authority inspections and strategic meetingQualifications & Experience RequirementsAdvanced degree in Life Science or Business with a post graduate qualification (PhD, MD, MBA or other).15+ years' experience in the pharmaceutical industry, at least 10 years' experience in Global Regulatory Affairs; biologics regulatory experience preferred.10+ years' leadership experience, including managing global regulatory teams.Different qualifications or responsibilities may apply based on local legal and/or educational requirements.About CSL BehringCSL 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.To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at Our BenefitsFor more information on CSL benefits visit How CSL Supports Your Well-being | CSL.You Belong at CSLAt 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. To learn more about inclusion and belonging visit Equal Opportunity EmployerCSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit
-
APAC/LATAM Regulatory Affairs Hematology Lead
Vor 6 Tagen
EMEA, CH, Glattbrugg, CSL Behring CSL VollzeitCSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference...
-
Glattbrugg, Schweiz CSL VollzeitCSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference...
-
Sr. Dir., Global Regulatory Team Leader – Hematology
vor 11 Stunden
Glattbrugg, Schweiz CSL VollzeitSr. Dir., Global Regulatory Team Leader – Hematology & LCM Europe 1 week ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team...
-
EMEA, CH, Glattbrugg, CSL Behring CSL VollzeitCSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference...
-
Global Regulatory Affairs Clinical Solutions
Vor 4 Tagen
Glattbrugg, Schweiz Vifor Pharma Vollzeit-CSL Vifor is a world leading Nephrology, Iron Deficiency and Cardio-Renal pharmaceutical company, we are experiencing rapid growth due to pipeline realization, optimization and innovative alliance partnerships on a global basis. A position has arisen within the Global Regulatory Affairs function in our Clinical Solutions Team for Manager to focus on...
-
Regulatory Affairs Manager
vor 3 Wochen
Glattbrugg, Opfikon, ZH, Schweiz Coopers Group AG VollzeitRegulatory Affairs Manager m/f/d, Zürich This role supports regulatory activities for the development, registration, and life-cycle management of vaccine candidates across Europe. The position manages assigned regulatory projects, including preparation and maintenance of dossier and Marketing Authorization Application (MAA) submissions, ensuring all filings...
-
Regulatory Affairs Manager
vor 3 Wochen
Glattbrugg, Opfikon, ZH, Schweiz Coopers Group AG VollzeitRegulatory Affairs Manager m/f/d, Zürich This role supports regulatory activities for the development, registration, and life-cycle management of vaccine candidates across Europe. The position manages assigned regulatory projects, including preparation and maintenance of dossier and Marketing Authorization Application (MAA) submissions, ensuring all filings...
-
Pharmacovigilance Quality Management Lead
vor 1 Woche
Glattbrugg, Schweiz Vifor Pharma VollzeitVifor Pharma is experiencing rapid pipeline optimization and growth in Nephrology, Cardio-Renal and Rare diseases. A position has arisen in the Pharmacovigilance Quality Assurance (GPvP) group in a leadership role to manage a talented team of PV Quality Auditors and take responsibility for all PV Quality Assurance related topics within the wider Clinical and...
-
Aviation Compliance Engineer — Regulatory
vor 2 Wochen
Glattbrugg, Schweiz SR Technics Holding VollzeitA leading engine MRO service provider in Zurich is seeking a Compliance Engineer to ensure regulatory compliance and update standards and procedures. The ideal candidate has a technical degree in aerospace or mechanical engineering and experience in compliance audits. Fluent English is required, and knowledge of civil aviation regulations is preferred. This...
-
Medical Communications Lead
vor 2 Wochen
Glattbrugg, Schweiz Experis Vollzeit**Medical Communication Lead** **Contact**:Francesca De Chirico **Start Date: ASAP** **Duration**:6** months - **chance to have further contract extension** **Location**:Glattbrugg** **Workload percentage**:100%** **Key Responsibilities**: - Lead EUCAN (Europe & Canada) Medical Education initiatives and publications to support Rare Disease portfolio...