Responsibilities:
• Under general supervision, carries out fundamental or applied research/processes in support of product development activities, QC assays, and/or patient sample analysis where required and reports results.
• Maintains technical documents, including laboratory notebooks and batch records.
• Develops, validates, and standardizes analytical methods.
• Contributes technology platform capabilities to team in order to achieve designated project objectives.
• Coordinates global and local research and development projects.
• Manages collaboration with different CSL sites and external partners.
Qualifications:
• Bachelors or postgraduate degree and /or extensive experience in relevant discipline
• Minimum 3 years laboratory experience with training in a relevant technical discipline eg. molecular and cellular biology, analytical biochemistry etc.
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Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
About CSL Vifor
CSL Vifor aims to become the global leader in iron deficiency and nephrology.
The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care.
For more information, please visit viforpharma.com
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As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.
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