Scientist, Bioassay Methods Development

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Company :
Johnson & Johnson Family of Companies

Location :
Malvern, Pennsylvania

Expiry Date :
Sun, 13 Dec 2020 23:59:59 GMT

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Description :
Job Details Full-timeEstimated: $67,000 – $94,000 a year2 hours ago Qualifications – Flow cytometry – CGMP – Laboratory experience – Immunoassays – Assays – Bachelor’s degree – Doctoral degree – Master’s degree Full Job Description Janssen Research & Development, L.L.C., a division of Johnson & Johnson’s Family of Companies is recruiting for a Scientist, Bioassay Methods Development to be located at the J & J site in Malvern, PA. At the Janssen Pharmaceutical Companies of Johnson & Johnson, 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. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow us @JanssenGlobal. Janssen Research & Development, LLC is part of the Janssen Pharmaceutical Companies. Key Responsibilities: The Scientist, Bioassay Methods Development will be responsible for development of assays such as cell-based bioassay and binding assays to be used 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 and also to be used as QC potency assays. itional responsibilities include, but are not limited to: Assay development, writing protocols, reports, and performing and coordinating testing to support manufacturing process development, process validations, and manufacturing investigations across functional groups. Responsibility for evaluation of new technologies method development, qualification, validation and transfer activities and represent Bioassay on Analytical sub teams Maintain laboratory notebooks and prepare written protocols and reports in a GMP compliant manner. Accurate capture of data in a timely fashion and entry into appropriate systems (e.g. LIMS), including maintenance of detailed records in compliance with applicable cGMP, safety, and environmental requirements is expected and the successful candidate will ensure data integrity and protocol compliance. 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 Writing analytical sections of regulatory submissions and will support regulatory filings including INDs and BLAs. Qualifications Qualifications: Education: Bachelor’s degree is required, in Biology, Chemistry, Pharmacology. Molecular Biology, Immunology, Microbiology or other relevant scientific field, with at least 6 or more years of industry experience is required. OR Master’s degree is required with at least 3 or more years of industry experience OR PhD with 1 or more years of relevant academic or industry experience is required. Required Experience and Skills: Knowledge of drug development, particularly, related to potency and structure function characterization is required. Experience with method development in a variety of cell-based bioassays and binding assays is required. Experience in immunochemical techniques, including flow cytometry and immunoassays or nucleic acid assays is required. The ability to communicate ideas and influence others is essential. Strong technical writing and verbal communication skills are required. Excellent interpersonal skills with ability to operate effectively in a dynamic work environment and team setting. Preferred Experience or Skills: Experience in immuno-oncology, neurobiology, and/or cardiovascular biology is strongly preferred. Experience with therapeutic proteins, including antibodies, cell and gene therapy and/or virology and/or vaccines is preferred. Prior experience in cGMP environment or experience with laboratory automation is preferred. Preferred skills would include method robustness, DoE, method design, and familiarity with assay validation parameters. Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law Primary Location United States-Pennsylvania-Malvern-200 Great Valley Parkway Organization Janssen Research & Development, LLC (6084) Job Function R & D Requisition ID W Show full job description Apply Now