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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 a Senior Scientist, Cell & Gene Therapy API, to be located in Malvern, PA.

Purpose: The candidate will join the Virology team to involve in and innovative API development activities for Cell & Gene Therapy programs. The role will include all aspects of API development work from platform evaluation, drug substance process development to viral safety and viral clearance. Working closely with functional teams within J& J Innovative Medicine, this individual is expected to be a key leader for viral safety and viral clearance studies. S/He will be accountable for driving viral safety investigations, virology related health authority quires, evaluate new technologies and platform for API development, and drive scientific excellence for the technical platforms. The candidate should be strongly motivated and dedicated, show initiative, and work independently. Troubleshooting skills are essential. They will demonstrate urgency, be organized, can work well in a team setting, show leadership and be sensitive to timelines. The scientist will effectively and frequently collaborate with colleagues in the Cell & Gene Therapy function, as well as with multidisciplinary teams at J& J to successfully drive various programs.

You will be responsible for:

• Oversee viral safety and viral clearance studies for investigations and regulatory requests for Cell & Gene Therapy programs and Biologics.
• Design and execute complex and scientifically demanding experiments for projects within the framework of a small team. Provide high quality data in a timely fashion, including drafting and executing technical reports.
• Provide Virology expertise to address health authority queries and regulatory filings.
• Partner effectively with stakeholders & partners for API related activities. Drive initiatives to increase speed and flexibility, as well as efficiency, of development processes through consistent demonstration of scientific rigor and operational excellence.
• Work closely with CRO/CDMO companies to coordinate and manage external studies to advance projects.
• Manage multiple experiments/projects simultaneously.
• Contribute on various projects outside of their own and collaborate with stakeholders from all relevant functions.
• Provides scientific and technical expertise to support process development activities of Cell & Gene Therapy programs. Tech transfers to ensure processes are successfully scaled-up.
• Keep up to date with the literature related to their field. Act as an expert resource in their scientific field and in related disciplines.

Qualifications/Requirements:

Education: Minimum of a Master’s Degree in Virology is required. PhD is preferred.

Skills/Experience:

Required:

• A minimum of 4 years of research experience in Viral vector engineering, or Viral Safety and Viral Clearance, or Process development of viral vectors and viral analytics. For PhD, 2 years are required.
• A minimum of 2 years of pharmaceutical industry experience is required.
• CMC experience in drug substance process development and regulatory filings is required.
• Hands-on experience in Virology, Cell and Molecular biology techniques (cell culture, transfections, transductions, qRT-PCR, ELISA, Plaque assays, virus neutralization assays) is required.
• Critical thinker with excellent time management and delivery focus, able to independently strategize and design/execute and accurately interpret complex scientific experiments and data at a group level across multiple programs is required.
• Highly motivated self-starter, proactive and able to excel within a matrix organization is required.
• Fluent in written and spoken English with excellent communication, interpersonal and collaborative skills is required.

Preferred:

• Experience with lentivirus, AAV and oncolytic viruses.
• Experience with Next Generation Sequencing platforms and data analysis pipelines
• Experience in the regulatory filing and addressing health authority requests
• cGMP knowledge
• Experience in working with cross-functional teams

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, please contact us via https: //www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource

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