ppAt Johnson Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 jnj.com. /ppAs 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. /ph3Job Function /h3pSupply Chain Engineering /ph3Job Sub Function /h3pProcess Engineering /ph3Job Category /h3pScientific/Technology /ph3All Job Posting Locations /h3pBeerse, Antwerp, Belgium, Latina, Italy /ph3Job Description /h3pJohnson Johnson Inc. is recruiting for an MSAT Synthetics Drug Product External site Pr. Scientist /ppMSAT (Manufacturing Science and Technology) is a division of the Innovative Medicine Supply Chain (IMSC) of Johnson Johnson. MSAT is a worldwide organization with members located across the geography in close vicinity to the Internal Manufacturing Network (MTO) and External Manufacturers, providing Technical Competence and Manufacturing Excellence to Johnson and Johnson’s pharmaceutical environment and product portfolio. /ppThe MSAT Synthetics DP External Site Pr. Scientist is responsible for providing technical oversight to external manufacturing (EM) sites. They will also be responsible for site ownership in performing due diligence, auditing, and site onboarding. The Scientist will conduct technical/risk assessment, execution, and/or oversight of New Product Introduction (NPI), technical transfers, and Product Life Cycle (LCM) management. They will be involved with standards and new technology deployment, Multi-Variate Analysis (MVA) statistical analysis, Proactive assessments and de-risking of products and process through collaboration with various other MSAT teams, different functions, and partners. /ph3Key Responsibilities /h3ulliHandle execution of drug product technology transfer, product life cycle activities, material qualification,



and cleaning validation /liliSupport NPI using applicable tools and standards in collaboration with Virtual Management Team (VMT), key supply chain functions, Technical launch integrators / owners, and EM site /liliAct as Technical coordinator for CMO process technology proficiency assessment, technology standards, and implementation of MSAT Technology Roadmaps /liliServe as primary contact and site owner for technical issues related to EM and represent in VMT by being a single technical voice including EM, thus supporting decision / actions /liliMaintain and develop good understanding of the status regarding ongoing and future planned technical activities at site /liliEngage in Site Lifecycle processes (due diligence / selection, onboarding, engage, ongoing monitoring, disengage) including support to localization; also be involved in technical assessment / due diligence of product portfolio / in- licensing /liliSupport working models and tools in handling EM from technical perspective which includes Technical risk metrics Switching Effort / Complexity metric for fit-for-purpose segmentation model, and account planning/adherence /liliConduct technical assessment of change controls and other quality related activities by associating with Quality for audits and inspections /liliProvide technical support on site for investigations and resolution of deviation / OOS (process, cleaning, troubleshooting) by collaborating with engineering, product launch, and technical owners /li /ulh3Qualifications /h3h3Education /h3ulliMinimum of a Bachelor's/University or equivalent degree required; Master's or PhD and/or focused degree specialization in Engineering, Pharmaceutical Science, or equivalent technical subject is preferred /li /ulh3Required /h3h3Experience and Skills /h3ulliMinimum 8 years of relevant work experience /liliDemonstrated experience/expertise with various dosage forms, including experience in process science and tech transfer of Liquid solids manufacturing technology.



/liliExperience working with external manufacturing network (EM) /liliBasic knowledge of Small Molecule Supply chain (products, customers, suppliers, plants) /liliStrong communication and teamwork/networking skills with the ability to interact at different levels of the organization/sector /liliAbility to lead activities under general direction, and demonstrate a good sense of prioritization of assigned tasks goals and handle time accordingly /liliStrong understanding and knowledge of QC (Quality Compliance) and the regulatory requirements (e.g., GMP, EHSS, etc.) related to pharmaceutical manufacturing environment /li /ulh3Preferred /h3ulliExperience in specialized technology which includes Freeze dried tablets, Softgel capsules etc., new pharmaceutical manufacturing technology especially continuous manufacturing or related technology /liliUnderstanding and application knowledge in statistics and process excellence / investigation tools /li /ulh3Other /h3ulliMay require up to 25% travel, domestic and/or international depending on business needs /liliRequires the ability, through our flexible work policy, to work on-site a minimum of three days each week, with the option for two remote workdays each week and depending on business needs /li /ulp#SCEngineer /ph3Required Skills /h3h3Preferred Skills /h3h3The anticipated pay range for this position, in the primary posting location, is: /h3p€79,800.00 - €137,770.00 /ph3The anticipated pay ranges for additional locations are: /h3pItaly – The anticipated base pay range for this position is €56,100.00 – €96,945.00 /ph3Benefits /h3ulliannual premio with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. /lilivacation days /liliparental leave for a minimum of 12 weeks /lilibereavement leave /lilicaregiver leave /lilivolunteer leave /liliwell-being reimbursement /liliprograms for financial, physical and mental health. /liliservice anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. /li /ulpThis is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change. /p /p #J-18808-Ljbffr

📌 MSAT Synthetics Liquid DP External site Principal Scientist (Latina)
🏢 Johnson & Johnson Innovative Medicine
📍 Latina