Experienced Scientist, Bioassay Methods Development

Johnson and Johnson is currently seeking 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.

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 https://www.jnj.com/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.

Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.

Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.
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 success...