Scientist, Process Analytical Sciences - Biologics AD
About The Position
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. About Innovative Medicine 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 https://www.jnj.com/innovative-medicine We are searching for the best talent for a Scientist in the Process Analytical Sciences team located in Malvern, PA. The Scientist, Process Analytical Sciences (PAS), is part of the Analytical Development (AD) Proteins organization and is responsible for accelerating large-molecule development by delivering phase-appropriate analytical testing at scale—combining high-throughput methods, automation, and streamlined data workflows to meet program timelines.
Requirements
- Minimum of a bachelor’s degree in chemistry, biology, biochemistry, engineering, or related scientific/technical field with 3-5 years of relevant industry experience or a master’s degree with 1-3 years of experience.
- Hands-on experience with laboratory automation platforms, including Tecan (EVO/Fluent) or similar liquid-handling systems, with demonstrated capability in scripting and workflow development.
- Experience working in cross-functional environments, effectively collaborating with analytical scientists, engineers, digital/data teams, and external vendors.
- Strong background in multiple protein-based technologies (e.g., HPLC/UPLC, cIEF, CE-SDS, ELISA, cell-based assays, etc.)
Nice To Haves
- Experience with programming or scripting concepts (e.g., EVOware, FluentControl, Python, or similar) and integration of automated systems with data platforms (ELN/LIMS).
- Demonstrated ability to train and mentor others, create standard work, and build sustainable technical capability within a team environment.
- Strong communication, organization, and project management skills, with the ability to prioritize work and deliver against timelines in a dynamic environment.
- Familiarity with regulated environments (e.g., GMP/GxP) and supporting documentation, validation, and data integrity requirements.
- Proven experience translating manual analytical or sample preparation workflows into automated solutions, supporting biologics development or protein-based assays.
Responsibilities
- Conduct execution of protein-based analytical assays for biologics drug development to quantify size variants, excipient content, charge variants, bioactivity, etc.
- Troubleshoot instrumentation issues; perform root-cause investigations with SMEs/vendors and implement corrective actions.
- Thrive in a team setting in a dynamic environment, contribute technical expertise to multiple large molecule programs, be proficient with documentation, and review of analytical data
- Design and deploy Tecan-automated sample prep workflows supporting protein-based assays and day-to-day analytical testing needs.
- Create and maintain Tecan scripts/methods (liquid classes, labware definitions, prompts, sample sheets, error handling) for reliable execution.
- Train and mentor end-users to run and maintain scripts; publish templates and standard processes to build shared capability.
- Evaluate and pilot new automation devices/integrations; summarize feasibility results and recommend expansions to workflow scope.
Benefits
- inclusive work environment where each person is considered as an individual
- respect the diversity and dignity of our employees and recognize their merit
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
