Senior Scientist, Biotherapeutics R&D
Malvern, PA - USA
Job Summary
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .
As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:
Biotherapeutics R&DJob Category:
Scientific/TechnologyAll Job Posting Locations:
Malvern Pennsylvania United States of AmericaJob 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 & Johnson Innovative Medicine R&D is recruiting for a Senior Scientist Biotherapeutics R&D. This position is a hybrid role and will be located in Malvern PA.
The Senior Scientist Biotherapeutics R&D will be responsible for the management negotiation and execution of license and business continuity agreements for cell lines and critical reagents. This individual will coordinate institutional knowledge for cell lines used in Quality Control (QC) release for Analytical Development. Ensure timely submission and execution of single service agreements and confidentiality agreements for generation of custom reagents cell lines and business continuity agreements. Ensure license obligations are met with timely payment and invoicing
Principal Responsibilities:
Conceptualization/Creation Ideation and Execution:
Independently hypothesize design and execute projects or analysis with hands-on involvement.
Operations Management:
Ensure the availability of cell lines and critical reagents governed by contract.
Guide the examination of standard procedures and improves current approaches.
Information Management and Communication:
Engage with Legal to confirm Freedom to Operate and status of Intellectual Property.
Manage historical contract knowledge and optimization of contract tracking and payment.
Communicate regularly with business functions responsible for contract generation and maintenance including Procurement Contracting Totality and others.
Project Management
Collaborate across research groups to share results.
Leverage the work of project members to meet project checkpoints and accomplish team objectives on time and within budget.
Qualifications:
A minimum of a Bachelors degree in Biology Pharmacology. Immunology Biochemistry or other relevant scientific discipline is required. Advanced degree (Masters Ph.D.) in Biology Pharmacology. Immunology Biochemistry or other relevant scientific discipline is preferred.
A minimum of 5 years of relevant industry experience with a Bachelors degree; a minimum of 3 years of relevant industry experience with a Masters degree; or a minimum of 1 year of relevant industry experience with a Ph.D. is required.
Experience with method development is required.
Understanding of the critical components for method development is required.
Understanding of cell lines and critical reagent methods preferred.
Knowledge of the requirements and obligations for analytical method components for use in the release of clinical and commercial products is preferred.
Knowledge of execution of scientific contracts and licenses is preferred.
Demonstrated ability to collaborate with internal and external stakeholders is required.
Must have excellent verbal and written communication skills.
Must have be highly organized with a strong attention to detail.
Must have strong problem-solving skills.
The ability to work independently with minimal supervision to meet tight deadlines is required.
The ability to engage with cross-functional teams and Business and Quality groups to drive the execution of agreements is required.
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 and 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 email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.
#LI-Hybrid
Required Skills:
Preferred Skills:
Analytical Reasoning Biochemistry Biotechnology Chemistry Manufacturing and Control (CMC) Clinical Research and Regulations Clinical Trial Designs Collaboration Data Synthesis Drug Discovery Development Molecular Diagnostics Pharmacovigilance Process Improvements Productivity Planning Program Management Scientific Research Tactical Planning Technical CredibilityRequired Experience:
Senior IC
About Company
About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more