MSAT SM DP EXTERNAL SENIOR SCIENTIST

Janssen-Cilag S.
.
, a member of the Johnson & Johnson Family of Companies, is recruiting for a MSAT Small Molecule Drug Product (SM DP) Senior Scientist! 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 at https://www.
nj.
om/.
Are you interested in joining a global and diverse team that is helping improve patient care and drive innovation? Apply today for this exciting opportunity! MSAT (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.
The MSAT SM DP External Senior Scientist will provide Technical oversight to external manufacturing 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.
Key Responsibilities.
Handle execution of drug product technology transfer, product life cycle activities, material qualification, and cleaning validation Support NPI using applicable tools and standards in collaboration with Virtual Management Team (VMT), key supply chain functions, Technical launch integrators / owners and EM site Act as Technical coordinator for CMO process technology proficiency assessment, technology standards and implementation of MSAT Technology Roadmaps Serve as primary contact and site owner for technical issues related to EM and represent in VMT by being single technical voice including EM, thus supporting decision / actions Maintain and develop good understanding of the status regarding ongoing and future planned technical activities at site Engage and influence decisions of Site Lifecycle processes (Due diligence / Selection, Onboarding, Engage, Ongoing Monitoring, Disengage) including support to localization; also involved in technical assessment / due diligence of product portfolio / in- licensing Support 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 Conduct technical assessment of change controls and other quality related activities by associating with Quality for audits and inspections Provide technical support on site for investigations and resolution of deviation / OOS (process, cleaning, troubleshooting) by collaborating with engineering, product launch and technical owners Qualifications Education.
Minimum 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 Experience and Skills.
Required.
Minimum 8 years of relevant work experience Demonstrated experience/expertise with various dosage forms, including experience with solids manufacturing technology, process, and transfer Experience working with external manufacturing network (CMO) Basic knowledge of Small Molecule Supply chain (products, customers, suppliers, plants) Strong communication and collaboration/networking skills with the ability to interact at different levels of the organization/sector Ability to lead activities under general direction, and demonstrate a good sense of prioritization of assigned tasks & goals and handle time accordingly Strong understanding and knowledge of Q&C (Quality & Compliance) and the regulatory requirements (e.
., GMP, EHSS, etc.) related to pharmaceutical manufacturing environment Preferred.
Experience in new pharmaceutical manufacturing technology especially OROS technology, continuous manufacturing, or related technology Understanding and application knowledge in statistics and process excellence / investigation tools Other.
May require up to 25% travel, domestic and/or international depending on business needs Requires 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 Why join Johnson & Johnson Working at Johnson & Johnson is more than a job.
We are changing the trajectory of Human Health and working with Johnson & Johnson can change everything.
Including you.
Learn more by watching this video.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Johnson & Johnson provides reasonable accommodation in job application procedures for qualified individuals with disabilities and disabled veterans.
Want to find out more about what it’s like working for Johnson & Johnson from the personal level? Please visit career stories.
On our career website, you can also learn about our hiring process.