Experienced Scientist, Biotherapeutics R&D

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Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 .

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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

Johnson & Johnson Innovative Medicine R&D is recruiting for an Experienced Scientist, Biotherapeutics R&D.

This position is a hybrid role and will be located in Malvern, PA.

Purpose:

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 the 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.

You will be responsible for:


* 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...