Senior Principal Scientist, Tech Ops (CMC Science) - Recombinant

Posted 3 Days Ago
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41 Locations
Remote
Senior level
Biotech
The Role
Lead technical workstreams in recombinant process science to support product lifecycle management. Provide scientific oversight for process changes, technology transfers, validation, and risk assessments. Collaborate cross-functionally across manufacturing, quality, and regulatory teams, contribute to product strategy, implement continuous improvements, and mentor junior scientists.
Summary Generated by Built In
Senior Principal Scientist, TechOps (CMC Science) – Recombinant

This role is Global and can be based in Bern, CH, Marburg DE, King od Prussia, PA USA or Kankakee IL USA

Job Purpose

The Senior Principal Scientist is a recognized technical expert within the Recombinant Integrated Product Team (IPT), providing advanced scientific expertise and leading complex technical activities to support product lifecycle management.

The role contributes to the execution of product strategies by delivering high-quality scientific input, leading defined technical initiatives, and supporting cross-functional decision-making to ensure robust product performance and continuous improvement.

Main Responsibilities & Accountabilities

1. Technical Expertise and Workstream Leadership

  • Acts as a subject matter expert in recombinant process science, providing advanced technical knowledge to support complex product-related activities.
  • Leads defined technical workstreams or projects within broader product initiatives.
  • Delivers high-quality scientific outcomes in line with project objectives, timelines, and performance expectations.

2. Contribution to Product Strategy and Planning

  • Contributes technical input to the development and refinement of the product technical roadmap.
  • Identifies and evaluates improvement opportunities (e.g., process robustness, yield, compliance) and supports their assessment and implementation.
  • Provides scientific input into business cases and supports data-driven decision-making processes.

3. Cross-Functional Collaboration

  • Works within a global, matrixed IPT environment, collaborating with Manufacturing, MS&T, Quality, and Regulatory functions.
  • Supports alignment of technical activities across sites and functions.
  • Engages with stakeholders to ensure effective execution of product-related initiatives.

4. Scientific Oversight and Technical Support

  • Ensures application of sound scientific principles and compliance in product lifecycle activities, including process changes and technology transfers.
  • Provides input to technical decision-making processes, including change controls, validation strategies, and lifecycle management activities.
  • Supports data analysis, process understanding, and technical risk assessments.

5. Continuous Improvement and Innovation

  • Contributes to the identification and implementation of process improvements and efficiency gains.
  • Applies scientific methodologies and data analysis to improve process consistency and product quality.
  • Supports implementation of best practices and innovative approaches within the IPT.

6. Stakeholder Interaction and Communication

  • Communicates complex technical information clearly to cross-functional stakeholders.
  • Contributes to technical discussions and governance forums as required.
  • Builds effective working relationships to support delivery of product objectives.

7. Coaching and Knowledge Sharing

  • Provides guidance and informal mentoring to junior scientists and team members.
  • Contributes to knowledge sharing and continuous development of technical capabilities within the organization.

Qualifications & Experience Requirements

  • PhD in Biochemistry, Biotechnology, Chemical Engineering, or related Life Sciences discipline.
  • Typically 8–12 years of relevant experience in biopharmaceutical development and/or manufacturing within a GMP environment.
  • Strong expertise in recombinant product process development, manufacturing, and lifecycle management.
  • Experience contributing to complex technical projects in a matrix environment.
  • Solid understanding of process validation, technology transfer, and regulatory requirements.
  • Demonstrates strong project management skills, including planning, coordination, and execution of multiple projects to ensure timely delivery of objectives.

About CSL Behring

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.

Skills Required

  • PhD in Biochemistry, Biotechnology, Chemical Engineering, or related Life Sciences discipline.
  • 8-12 years relevant experience in biopharmaceutical development and/or manufacturing within a GMP environment.
  • Strong expertise in recombinant product process development, manufacturing, and lifecycle management.
  • Experience contributing to complex technical projects in a matrix environment.
  • Solid understanding of process validation, technology transfer, and regulatory requirements.
  • Strong project management skills, including planning, coordination, and execution of multiple projects.
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The Company
HQ: King of Prussia, PA
20,401 Employees

What We Do

CSL is a leading global biotechnology company with a dynamic portfolio of lifesaving medicines, including those that treat haemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency, dialysis and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies. Today, CSL – including our businesses, CSL Behring, CSL Seqirus, CSL Plasma and CSL Vifor – provides lifesaving products to patients in more than 100 countries and employs 32,000 people. Our unique combination of commercial strength, R&D focus and operational excellence enables us to identify, develop and deliver innovations so our patients can live life to the fullest. See our community guidelines: https://bit.ly/3Bs17Ra

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