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Associate Director, Project Management, Tech Ops
- Surpierre, Fribourg, Switzerland
- Surpierre, Fribourg, Switzerland
Über
Position Description Summary
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
Supports the team in leveraging technology platform capabilities to contribute to project goals.
Assists in the coordination of local and global research and development activities under guidance.
Participates in collaborative efforts with other CSL sites and external partners, with supervision.
Applies foundational knowledge of relevant scientific disciplines to support laboratory tasks and project execution.
Works under close to moderate supervision to meet operational objectives with limited impact on broader departmental outcomes.
Resolves routine problems and contributes to discussions on more complex issues with support from senior team members.
Communicates effectively within the team, sharing relevant information and adhering to established policies and procedures.
Qualifications & Experience Requirements
Bachelor’s degree in a relevant scientific discipline (e.g., molecular biology, cellular biology, biochemistry, or related field).
Up to 2 years of laboratory or research experience, including internships or academic lab work.
Familiarity with basic laboratory techniques and safety protocols.
Strong willingness to learn and grow within a collaborative research environment.
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 and CSL Plasma at .
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
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 .
Sprachkenntnisse
- English
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