MSAT Assistant Scientist
pAt 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, 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: /h3pQuality Engineering /ph3Job Category: /h3pScientific/Technology /ph3All Job Posting Locations: /h3pLatina, Italy /ph3Job Description: /h3h3MSAT ASSISTANT SCIENTIST /h3h3Temporary Contract – 12Months /h3pFor the Johnson Johnson Innovative Medicine manufacturing site in Latina (Italy), we are looking for an MSAT Assistant Scientist to join the Manufacturing Science Technology (MSAT) Department. /ppThe successful candidate will operate in a highly cross-functional environment,supportingprojects related tonew product introductions, manufacturing process improvements, compliance and inspection readiness activities, sustainability initiatives, operational excellence programs, and the implementation of innovative technologies. /ppWhile cleaning validation represents a key area of responsibility, the role extends well beyond validation execution and requires aproject management mindset, strongcommunication skills, and the ability to drive collaboration across multiple functions. /ppThe role is primarily focused on project coordination, stakeholder management, process improvement, and business manufacturing/packaging initiatives. /ppSuccess in this role requires the ability to manage projects, influence stakeholders, solve complex problems, and effectively communicate with teams across Manufacturing, Quality, Engineering, Supply Chain, and external partners. /ph3Main Responsibilities /h3pCoordinate and drive cleaning validation projects supporting New Product Introductions (NPI), Life Cycle Management (LCM), and Base Business activities. /ppPlan, monitor, and drive project execution by coordinating activities across Manufacturing, Quality, Engineering, Supply Chain, and external partners. /ppManage change controls and support impact assessments related to new products, process improvements, and manufacturing changes. /ppReview technical documentation,
including validation protocols, reports, risk assessments, and project records. /ppFacilitate project meetings, support decision-making processes, and ensure effective communication among stakeholders. /ppSupport investigations, root cause analysis, and risk assessments related to manufacturing and validation activities. /ppDrive innovation and continuous improvement initiatives through the evaluation and implementation of new cleaning technologies, digital solutions, process optimization opportunities, and operational excellence projects. /ppContribute to sustainability, Environmental Health Safety (EHS), and Continuous Improvement Programs (CIP) aimed at improving manufacturing performance, reducing environmental impact, and enhancing site efficiency. /ppBuild strong relationships with internal stakeholders and external partners, supporting technical discussions and project execution from concept to implementation. /ppSupport regulatory inspections, customer audits, and compliance-related activities, contributing to the maintenance of high quality and GMP standards. /ppIdentify and promote innovative solutions that improve compliance, quality, efficiency, sustainability, and overall business performance. /ph3Qualifications /h3pRequired: /ppMaster's Degree in Engineering, Pharmacy, Chemistry, CTF, Biotechnology, or related scientific disciplines. /ppFluent Italian and English is mandatory (written and spoken). /ppStrong project management, planning, and organizational skills. /ppExcellent communication and stakeholder management skills. /ppAbility to work effectively in a dynamic, cross-functional manufacturing environment. /ppAbility to manage multiple priorities and deliver results under tight timelines. /ppStrong problem-solving and decision-making capabilities. /ppHigh learning agility and willingness to rapidly acquire new technical competencies. /ppStrong sense of ownership, accountability, and continuous improvement. /ppStrong understanding of GMP compliance and inspection readiness principles, with the ability to support regulatory inspections, customer audits, internal quality audits, impact assessments, investigations, change management activities, corrective actions, and quality improvement initiatives. /ppPreferred: /ppPrevious experience in project management activities within MSAT,
Cleaning Validation, Process Validation, Technology Transfer, Manufacturing Support, Continuous Improvement, or related pharmaceutical technical functions will be considered a strong plus. /ppExperience in GMP-regulated manufacturing environments. /ppWorking knowledge of SAP, COMET, eLIMS, Power BI, or similar digital tools. /ph3What We Are Looking For /h3pWe are looking for a proactive, energetic, and highly motivated professional eager to learn, grow, and make an impact in a dynamic manufacturing environment. /ppThe ideal candidate enjoys coordinating projects, interacting with a wide range of stakeholders, and driving improvements across a complex organization. Strong communication skills are essential, as the role requires frequent interaction with operators, engineers, quality professionals, managers, suppliers, customers, and auditors. /ppThe successful candidate will be able to build effective relationships, influence decisions, communicate effectively at different organizational levels, and translate opportunities into concrete actions and results. /ph3Why Join MSAT? /h3pThis position offers a unique opportunity to develop expertise across manufacturing, project management, compliance, innovation, sustainability, and continuous improvement, while supporting the introduction of new products and technologies in a GMP-regulated environment. /ppYou will work at the intersection of Manufacturing, Quality, Engineering, Compliance, EHS, and Supply Chain, contributing to initiatives that shape the future of pharmaceutical manufacturing and help deliver innovative healthcare solutions to patients worldwide. /pp#SCEngineer /pp#LI-AA2 /ph3The anticipated base pay range for this position is: /h3p€30,400.00 - €49,450.00 /ph3Benefits: /h3pIn addition to base pay, we offer the following benefits*: an annual 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. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service 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. For more information, visit Employee benefits | Supporting well-being career growth | Johnson Johnson Careers. /pp*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change. /p #J-18808-Ljbffr
including validation protocols, reports, risk assessments, and project records. /ppFacilitate project meetings, support decision-making processes, and ensure effective communication among stakeholders. /ppSupport investigations, root cause analysis, and risk assessments related to manufacturing and validation activities. /ppDrive innovation and continuous improvement initiatives through the evaluation and implementation of new cleaning technologies, digital solutions, process optimization opportunities, and operational excellence projects. /ppContribute to sustainability, Environmental Health Safety (EHS), and Continuous Improvement Programs (CIP) aimed at improving manufacturing performance, reducing environmental impact, and enhancing site efficiency. /ppBuild strong relationships with internal stakeholders and external partners, supporting technical discussions and project execution from concept to implementation. /ppSupport regulatory inspections, customer audits, and compliance-related activities, contributing to the maintenance of high quality and GMP standards. /ppIdentify and promote innovative solutions that improve compliance, quality, efficiency, sustainability, and overall business performance. /ph3Qualifications /h3pRequired: /ppMaster's Degree in Engineering, Pharmacy, Chemistry, CTF, Biotechnology, or related scientific disciplines. /ppFluent Italian and English is mandatory (written and spoken). /ppStrong project management, planning, and organizational skills. /ppExcellent communication and stakeholder management skills. /ppAbility to work effectively in a dynamic, cross-functional manufacturing environment. /ppAbility to manage multiple priorities and deliver results under tight timelines. /ppStrong problem-solving and decision-making capabilities. /ppHigh learning agility and willingness to rapidly acquire new technical competencies. /ppStrong sense of ownership, accountability, and continuous improvement. /ppStrong understanding of GMP compliance and inspection readiness principles, with the ability to support regulatory inspections, customer audits, internal quality audits, impact assessments, investigations, change management activities, corrective actions, and quality improvement initiatives. /ppPreferred: /ppPrevious experience in project management activities within MSAT,
Cleaning Validation, Process Validation, Technology Transfer, Manufacturing Support, Continuous Improvement, or related pharmaceutical technical functions will be considered a strong plus. /ppExperience in GMP-regulated manufacturing environments. /ppWorking knowledge of SAP, COMET, eLIMS, Power BI, or similar digital tools. /ph3What We Are Looking For /h3pWe are looking for a proactive, energetic, and highly motivated professional eager to learn, grow, and make an impact in a dynamic manufacturing environment. /ppThe ideal candidate enjoys coordinating projects, interacting with a wide range of stakeholders, and driving improvements across a complex organization. Strong communication skills are essential, as the role requires frequent interaction with operators, engineers, quality professionals, managers, suppliers, customers, and auditors. /ppThe successful candidate will be able to build effective relationships, influence decisions, communicate effectively at different organizational levels, and translate opportunities into concrete actions and results. /ph3Why Join MSAT? /h3pThis position offers a unique opportunity to develop expertise across manufacturing, project management, compliance, innovation, sustainability, and continuous improvement, while supporting the introduction of new products and technologies in a GMP-regulated environment. /ppYou will work at the intersection of Manufacturing, Quality, Engineering, Compliance, EHS, and Supply Chain, contributing to initiatives that shape the future of pharmaceutical manufacturing and help deliver innovative healthcare solutions to patients worldwide. /pp#SCEngineer /pp#LI-AA2 /ph3The anticipated base pay range for this position is: /h3p€30,400.00 - €49,450.00 /ph3Benefits: /h3pIn addition to base pay, we offer the following benefits*: an annual 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. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service 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. For more information, visit Employee benefits | Supporting well-being career growth | Johnson Johnson Careers. /pp*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change. /p #J-18808-Ljbffr