Experienced Scientist
Company: 6084-Janssen Research & Development Legal Enti
Location: Malvern
Posted on: April 1, 2026
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Job Description:
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. Job Function:
Discovery & Pre-Clinical/Clinical Development Job Sub Function:
Biotherapeutics R&D Job Category: Scientific/Technology All Job
Posting Locations: Malvern, Pennsylvania, United States of America
Job Description: 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 an Experienced Scientist, Bioassay Methods
Development, located in Malvern, PA. The Experienced Scientist,
Bioassay Methods Development, will be responsible for the
development of cell-based bioassays and binding assays to be used
as QC potency assays and in support of structure-function and
biological characterization studies, to better understand mechanism
of action for new molecular entities in clinical development and
for commercial products. The individual will be accountable for
method development, qualification, validation, and transfer
activities as well as the evaluation of new technologies. Key
Responsibilities: Authoring protocols and reports. Performing and
coordinating testing to support analytical development,
manufacturing process development, process validations, and
manufacturing investigations across functional groups. Accurately
recording data in a timely manner, including maintenance of
detailed records in compliance with applicable GMP, safety, and
environmental requirements. The successful candidate will ensure
data integrity and protocol compliance. Designing, troubleshooting,
and executing experiments independently. Analyzing data,
interpreting results, and reporting data in laboratory notebooks.
Collaborate with partners to troubleshoot assay problems as they
occur. Maintain awareness of the current literature relevant to
methods. Writing analytical sections of regulatory submissions is
encouraged. The Scientist will support regulatory filings including
INDs and BLAs. Providing technical support with development and QC
laboratories is expected and the successful candidate will also
support Quality Assurance, Regulatory Affairs and Process
Development groups for all phases of product development as well as
ongoing support of analytical methods for marketed products.
Qualifications Education: A minimum of a Bachelor's degree in
Biology, Pharmacology. Immunology, Biochemistry, or other relevant
scientific field, with at least 4 years of industry experience, or
a Master's degree with at least 2 years of industry experience or
relevant academic experience. Experience and Skills: Required:
Experience in development of bioassays, binding assays, and/or
immunochemical techniques. Experience with cell culture and aseptic
technique. The ability to communicate ideas and influence others is
essential. Strong technical writing and verbal communication
skills. Excellent interpersonal skills with the ability to operate
effectively in a dynamic work environment. Preferred: Experience
with flow cytometry. Experience with Biacore and/or other surface
plasmon resonance technology. Experience with automated liquid
handlers (e.g. Tecan or Hamilton). Prior experience in the
biotechnology or pharmaceutical industry (therapeutic
proteins/antibodies, cell and gene therapies, and/or vaccines).
Prior experience in a GMP environment and experience with
laboratory automation. Preferred skills would include method
robustness, DoE, method design, and familiarity with assay
validation parameters. This job posting is anticipated to close on
April 2, 2026. The Company may however extend this time-period, in
which case the posting will remain available on
https://www.careers.jnj.com to accept additional applications.
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 & 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, external applicants please contact us via
https://www.jnj.com/contact-us/careers , internal employees contact
AskGS to be directed to your accommodation resource. LI-Onsite
Required Skills: Preferred Skills:
Keywords: 6084-Janssen Research & Development Legal Enti, Toms River , Experienced Scientist, Science, Research & Development , Malvern, New Jersey
