POST DOC MSAT LM DP INNOVATION

MSAT Emerging Technology is recruiting for a Post-Doc, located in Schaffhausen! Manufacturing Science & Technology (MSAT) Emerging Technology plays a key role in driving technology innovation for the J&J Innovative Medicine Supply Chain.
Emerging Technology is responsible for the definition of new opportunities, breakthrough-technology scouting, lab-scale proof-of-principle studies, and demonstrating proof-of-concept at large scale.
Our team develops and delivers projects that are primarily related to two key MSAT strategic pillars.
Process Intensification and Integrated Quality & Real-Time Release.
Our team reimagines the way we run and control our manufacturing processes! Thereby, driving key advancements in yield, reliability, and efficiency end-to-end.
To accelerate the delivery of proof-of-principle & proof-of-concept packages for Manufacturing of Large Molecules / Biologics, we are looking for a motivated Post-Doc based in Schaffhausen.
General Responsibilities.
Your key responsibility is to lead innovation projects for process intensification of biopharmaceutical manufacturing with deep scientific and technical expertise, analytical and manufacturing know-how together with our lab-based scientists and partners in R&D and Supply Chain.
Through active partnering within MSAT as well with key functions from R&D and across the supply chain, like Quality, Operations, and Digital, you play a key role in advancing technologies and process innovations.
Key Responsibilities Scientific Lead of Innovation Projects within Large Molecule Biologics Drug Product Mfg Scout and screen groundbreaking technologies in close collaboration with R&D by leading projects and ensuring consistency of the end-to-end solutions Project Leadership for PoP (lab-scale) and PoC (at-scale) studies, including project portfolio, risk management, and funding activities Business case development, in close alignment with Strategy & Deployment Preparation of and starting GMP integration.
Knowledge management & creation of documentation standards Other tasks Support other activities in the team and work area according to appropriate procedures, values, and standards on an ad-hoc basis as the need arises.
Support the Large Molecule Drug Product Innovation Community with project and portfolio management.
Qualifications Education.
PhD in an engineering field (preferred Biotechnology or Pharmaceutical related).
Past exposure to continuous manufacturing in a pharmaceutical setting is a plus.
Experience and Skills.
Required.
Past shown field experience in one or more of the following areas.
pharmaceutical (GMP) manufacturing technology (Drug Substance or Drug Product), continuous manufacturing, biotechnology, process analytical technology, analytical development, process engineering and/or system integration & automation.
Preferred.
Drug Product Biopharmaceutical Industrial knowledge or experience.
Experience with Continuous Manufacturing concepts.
Hands-on experience with Biopharmaceutical Analytical Technologies.
Background in process automation and control.
Familiarity with PAT tools and sensors with an understanding of digital architecture concepts for system integration.
Key competencies required.
Excellent problem-solving abilities, able to identify and address potential issues proactively and independently.
Excellent interpersonal and communication skills; flexible and adaptable Technological and digital curiosity Results and performance driven.
Ability to work with limited supervision and guidance.
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.