Scientist III
About the Client
They are a global biotechnology and life sciences organization, operating across multiple continents with a mission to advance health through innovation. Their success is built on the expertise and passion of the people-teams who collaborate to transform scientific breakthroughs into real-world solutions. They empower employees to take ownership of their careers, contribute meaningfully, and grow within a values-driven culture.
Job Opportunity: Scientist III, MSAT (Manufacturing, Sciences, & Technology)
This role offers an exciting opportunity to support the transfer and integration of viral vector bioprocesses into cGMP manufacturing environments. As part of a multidisciplinary team, the MSAT Scientist or Senior Scientist will collaborate closely with internal departments and external clients to ensure process readiness, scalability, and successful manufacturing execution.
Key Responsibilities:
Lead or support the transfer of biologic manufacturing processes by interpreting process flow diagrams, technical documentation, and process development data.
Facilitate the scale-up and technology transfer of upstream (e.g., cell culture, harvesting) and downstream (e.g., purification, formulation) bioprocess operations.
Work cross-functionally to manage and execute process transfers from process development teams or external clients in compliance with regulatory standards.
Oversee the execution of clinical or commercial manufacturing campaigns, troubleshoot process deviations, and guide investigations to determine root causes and corrective actions.
Collaborate with project managers to develop timelines, identify risks, and escalate critical issues as necessary.
Support new product introductions, process improvements, and ongoing manufacturing support by applying scientific and engineering principles.
Contribute to documentation such as bills of materials, material qualifications, and process descriptions to ensure consistent production outcomes.
Apply analytical tools and methodologies to monitor process performance and enhance operational efficiency.
Qualifications:
Bachelor's degree in biology, biochemistry, chemical engineering, biotechnology, or a related field.
Minimum 5 years of hands-on experience in biomanufacturing, preferably with a focus on viral vectors, biologics, or cell therapy products.
Solid understanding of bioprocess unit operations such as bioreactor setup, filtration systems, chromatography, and aseptic processing techniques.
Experience in sterile processing and/or fill-finish operations is a strong asset.
Strong analytical and critical thinking skills with the ability to resolve complex technical issues.
Effective communicator with the ability to convey technical concepts clearly across teams.
Demonstrated leadership in managing projects and coordinating with cross-functional stakeholders.
Familiarity with deviation management tools and root cause analysis methodologies (e.g., Fishbone, DMAIC, FMEA).
Detail-oriented with a high degree of accuracy in scientific documentation and process execution.
Experience with statistical analysis software or tools is a plus.