Ph3Overview /h3pJohnson Johnson believes 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 at /ph3Job Function /h3pTechnology Product Platform Management /ph3Job Sub Function /h3pTechnology Operations Support /ph3Job Category /h3pScientific/Technology /ph3All Job Posting Locations /h3pBeerse, Antwerp, Belgium; Latina, Italy /ph3Job Description /h3pJJ Innovative Medicines is recruiting a Formulation Scientist. /ppMSAT Small Molecule Drug Product is accountable for capturing and intensifying the scientific cornerstones for our innovative formulations and leading productivity, compliance, and sustainability throughout their commercial lifecycle. /ppYou will be responsible for scientific assessment and optimization of formulation process robustness, enhance product quality, and ensure regulatory compliance in the domain of liquid and/or solid dosage forms. The ideal candidate will have a strong background in pharmaceutical development and tech transfer with a passion for innovation and problem-solving. /ph3Responsibilities /h3ulliProvide technical support for technical transfer, PPQ, and commercial manufacturing operations, including sensitivity analysis, root cause analysis, and impact assessments. /liliPlan, design, execute, and document lab and plant studies related to formulation, and process optimization in support of commercialization and lifecycle management. /liliWrite, review, and approve protocols, reports, and regulatory submissions, and monitor market trends, competitive landscapes, and emerging regulations to inform strategic decision-making. /liliProvide subject matter expertise (SME) to prepare and support technical project reviews and operational excellence initiatives, and support or lead initiatives for compliance, resilience, formulation and process robustness optimization. /liliCollaborate with expert communities in development and supply chain to establish, maintain, and deploy best practices for formulation and process development and intensification, advancing the scientific foundations in Supply Chain. /liliLeverage networking and influencing skills to ensure effective collaboration with partners in RD and Supply Chain, and prepare and review relevant technical documents, such as risk assessments, change controls, regulatory submissions, deviations, validations, protocols, procedures, ... /li /ulh3Qualifications /h3ulliAdvanced degree in Pharmaceutics, Biotechnology, Engineering, Physics, or related area /liliMin 3 years of experience in development and tech transfer of solid dosage forms /liliStrong knowledge of the main liquid and solid dosage unit operations, IPCs, analytical release tests. Practical experience with PAT is a plus. /liliProficiency in utilizing statistical packages for experimental design and analysis. /liliExcellent analytical and problem-solving skills, with the ability to interpret data, identify trends, and draw actionable insights. /liliEffective interpersonal and communication skills, with the ability to articulate technical concepts to diverse audiences and collaborate effectively with cross-functional teams. /liliDemonstrated track record of project management, including the ability to prioritize tasks, meet deadlines, and deliver high-quality results. /liliStrong networking skills to establish and participate in academic and industry network. /liliGood presentation and technical writing skills. /liliKnowledge of regulatory requirements and guidelines related to pharmaceutical manufacturing (e.g., FDA, EMA, ICH) is preferred. /liliLanguage: English /li /ul /p #J-18808-Ljbffr