Sr Formulation Scientist
Johnson & Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 atFor 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.Job Description:J&J Innovative Medicines is recruiting a Sr Formulation Scientist.MSAT Small Molecule Drug Product is accountable for capturing and intensifying the scientific cornerstones and leading productivity, compliance, and sustainability throughout the commercial lifecycle.As a key member, you will be responsible for scientific assessment and optimization of formulation & process robustness, enhance product quality, and ensure regulatory compliance in the domain of(semi-)solid dosage forms. The ideal candidate will have a strong background in pharmaceutical sciences or physics with a passion for innovation and problem-solving.Responsibilities
o Sensitivity analysis: Guide experimentation to establish DS-properties meeting requirements for optimal DP-manufacturability.o BP²AL assessments.o Root cause analysis for quality, stability, and yield deviations.o Impact assessment of process variations, equipment modifications and raw material changes
QualificationsRequirements
Beerse, Anvers
Thu, 26 Sep 2024 07:32:06 GMT
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