Scientist, Bioassay Methods Development

Johnson & Johnson Innovative Medicine is recruiting for a Scientist in Bioassay Methods Development located in Malvern, PA.

At Johnson & Johnson,we believe health is everything.

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 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.
Scientist in Bioassay Methods Development Overview:

At Johnson & Johnson Innovative Medicine, we are working to create a world without disease.

Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.

We bring together the best minds and pursue the most promising science.

The 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.

Ma...