Scientist, Tech Ops

The Scientist, Tech Ops researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization.  Assesses, monitors and ensures products meet clinical safety standards.  Conducts sophisticated analysis, manages research information systems and technical documentation.  May be involved in providing para-professional laboratory support for product testing after collection. Establishes relationship with regulatory authorities to establish and maintain registration licenses to sell products globally.​

Designs and implements business experimental processes to enable product research and development. Designs related integrated process and candidate / product team activities and directs technical and operational activities to ensure planned project outcomes, and enables portfolio prioritization, resource allocation, and risk management. Provides and contributes to project progression and reports, as required, to project or program committees for decision-making support. Leads teams in the development of program and project strategy, and lifecycle management planning. Develops systems to support dynamic portfolio management. Serves a key role in portfolio evaluation process. Drives initiatives across research and development units to create fully integrated strategies. Monitors and reports on portfolio status and proactively addresses and resolves issues. May design and develop manufacturing processes for new or existing products, taking into consideration problems inherent in the transfer of technology from research to manufacturing. Develops procedures for the economical mass production in cooperation with pilot-plant and production departments. Conducts tests and measurements throughout stages of production to determine control over applicable variables.  As required, will need to operate within the current regulatory and compliance environments.​

Main Responsibilities & Accountabilities​

• 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.​
• Applies practical knowledge of job area typically obtained through advanced education and work experience​
• Works independently with general supervision to achieve operational targets with direct impact on departmental results​
• Problems faced are difficult but typically not complex, sometimes requiring understanding of broader set of issues​
• May influence others within the job area through explanation of facts, policies, and practices​

Qualifications & Experience Requirements​

• Bachelors or postgraduate degree and /or extensive experience in relevant discipline.​
• Minimum 3 years' laboratory experience with training in a relevant technical discipline e.g., molecular and cellular biology, analytical biochemistry etc.​
• Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.​

Are you interested? We are looking forward to receiving your online application.

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Über CSL Behring

CSL Behring ist ein weltweit führendes Unternehmen, das hochwertige Therapeutika für Menschen mit seltenen und ernsten Krankheiten entwickelt und vertreibt. Mit unseren Medikamenten für die Therapiegebiete Immunologie, Hämatologie, Herz-Kreislauf und Stoffwechsel, Atemwegserkrankungen und Transplantationsmedizin halten wir unser Versprechen, die Lebensqualität von Patienten in mehr als 100 Ländern zu verbessern. Erfahren Sie mehr über CSL Behring .

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