Principal Scientist, Early Development ADSI
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 Principal Scientist Early Development ASDI located in Malvern PA.
The Principal Scientist Early Development Analytical Development Scientific Integrator (ADSI) will be responsible for the following:
Provide strategic and technical leadership in analytical development and lead a cross-functional scientific team consisting of members from each of the AD sub-functions.
Represent AD on the CMC team and accountable for all AD project deliverables.
Lead the execution of critical quality attribute (CQA) assessment analytical control strategy and product specifications for programs.
Lead the analytical review of programs at governance meetings with support from subject matter experts.
Accountable for submission of complete consistent and high-quality regulatory documents to health authorities.
Effectively communicate project status/overview resources budget and issues to senior management.Accountable for project risk management including development of appropriate mitigation strategies and escalation to senior management.
Interact with and influence various stakeholders outside of Discovery Product Development and Supply (DPDS) including Manufacturing Regulatory Quality Discovery and external partners.
Qualifications:
A minimum of a Masters degree in Analytical Chemistry Biochemistry Biological Science or a related scientific discipline is required. A Ph.D. in Analytical Chemistry Biochemistry Biological Science or a related scientific discipline in preferred.
A minimum of 6 years of experience in biopharmaceutical development with a Masters degree or a minimum of 3 years of experience in biopharmaceutical development with a Ph.D. is required.
A minimum of 2 years of experience working on cross-functional CMC teams or analytical sub-teams is preferred.
Knowledge of biotherapeutic development and analytical strategies including analytical protein characterization separation techniques and biological potency assays is required.
Experience authoring and reviewing CMC sections of clinical trial applications (INDs/IMPDs) and addressing health authority questions is required.
Must have excellent communication interpersonal and negotiation skills.
Must have strong leadership skills.
The ability to collaborate across teams in a matrix environment is required.
The ability to lead and execute complex plans/deliverables in a matrix environment 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.
Required Skills:
Preferred Skills:
Analytical Reasoning Biochemistry Biotechnology Chemistry Manufacturing and Control (CMC) Clinical Research and Regulations Clinical Trial Designs Coaching Critical Thinking Drug Discovery Development Emerging Technologies Molecular Diagnostics Organizing Pharmacovigilance Presentation Design Process Improvements Productivity Planning Scientific ResearchRequired Experience:
Staff 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