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Job Function:
Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:
Biotherapeutics R&DJob Category:
Scientific/TechnologyAll Job Posting Locations:
Spring House Pennsylvania United States of AmericaJob Description:
We are searching for the best talent for our Associate Scientist Lentivirus Upstream Process Development position to be located in Spring House PA.
Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.
Learn more at Research & Development the Discovery Product Development & Supply (DPDS) organization is responsible for the development clinical supply marketed product support and life cycle management of Biotherapeutics. Within DPDS the API CGT group supports product development of novel cell and gene therapies for unmet medical needs.
We are seeking a motivated Associate Scientist to join our Lentivirus Small Scale Process Development team supporting upstream cell culture process development for lentiviral vectorbased cell and gene therapy products within DPDS API.
In this role you will integrate into the upstream development team and support the execution of experiments under the guidance of senior scientists and team leads. Responsibilities will focus on performing maintaining and monitoring cell cultures while collaborating closely with project teams to achieve development objectives.
The Associate Scientist will support experimental activities related to scaling viral vectorbased processes from shake flasks to bioreactor systems assist in identifying process parameters perform planned experiments and contribute to upstream cell culture process optimization. The role may also include participation in data analysis for early- and late-stage programs and providing support for technology transfer activities to GMP clinical or commercial manufacturing sites. Additional laboratory studies such as media optimization or evaluation of new upstream technologies may be performed as needed.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
Analytical Reasoning Biochemistry Chemistry Manufacturing and Control (CMC) Clinical Trial Protocols Collaborating Data Quality Drug Discovery Development Execution Focus Molecular Diagnostics Pharmacogenetics Problem Solving Research Documents Scientific Research Technologically Savvy Troubleshooting Written ExpressionRequired Experience:
IC
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