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
Qualifications & Experience Requirements
Are you interested? We are looking forward to receiving your online application.
CSL 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 https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.
Our Benefits
For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.
You Belong at CSL
At 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 https://www.csl.com/careers/inclusion-and-belonging
Equal Opportunity Employer
CSL 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 https://www.csl.com/accessibility-statement.