Senior Engineer, MSAT Biotherapeutic Drug Product

Das ist der Job

ppAt Johnson Johnson,we believe health is everything.

Darum lohnt es sich

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Defect Trending, Limit Recalculation /li liOwn and coordinate validation activities with internal partners /li liLead or contribute to multi-functional project teams, providing technical guidance and coordinating activities to meet quality, timeline, and compliance objectives /li liImplement process capability, quality, and cost improvement changes /li liSupport E2E technical guidance for product lifecycle activities, including Continued Process Verification (CPV) trending, change implementation, and continuous improvement /li liProvide technical feedback and assessments for deviations, investigations, CAPAs, and change controls related to drug product manufacturing processes /li liActive participation in internal, customer, and health authority inspections as lead Subject Matter Expert /li liMaintain excellent and collaborative relationships with all business partners /li liPerform statistical analyses on production data /li /ul h3Qualifications /h3 pbEDUCATION: /b /p ul liMinimum of a Bachelor's/University or equivalent degree is required; focused degree in Chemistry, Pharmacy, Engineering, or related field is preferred /li /ul h3Required /h3 ul liMinimum 4 years of relevant work experience /li liExperience in the Pharmaceutical, Biotechnology, and/or Life Science industry /li liDemonstrated ability to lead and execute projects, preferably as part of cross-functional teams and/or projects /li liStrong decision-making and problem-solving competencies, combined with excellent communication and negotiation skills /li liFlexible, motivated, team-player, open to new ideas and driving innovation /li /ul h3Preferred /h3 ul liProven experience supporting GMP manufacturing environments, including change control, lifecycle management activities, and hands‑on leadership of GMP investigations /li liStrong background in drug product manufacturing, MSAT, process validation, tech transfer, and optical inspection related topics /li liSolid knowledge of Quality Assurance, Regulatory Compliance, cGMP requirements, and EHS /li liFamiliarity with statistical or data analysis tools (e.g., Minitab or similar) and use of production or quality data to support process understanding /li /ul h3Other /h3 ul liRequires proficiency in English (oral and written); basic proficiency in German is strongly preferred /li liMay require up to 10% domestic and/or international travel /li liRequires 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 /li /ul h3Required Skills /h3 h3Preferred Skills /h3 pAgile Decision Making, Coaching, Corrective and Preventive Action (CAPA), Critical Thinking, Emerging Technologies, Issue Escalation, Lean Supply Chain Management, Problem Solving, Process Control, Process Engineering, Product Costing, Product Improvements, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Technical Research, Technologically Savvy, Validation Testing, Vendor Selection /p /p 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. /p pAs 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. /p h3Job Function /h3 pSupply Chain Engineering /p h3Job Sub Function /h3 pProcess Engineering /p h3Job Category /h3 pScientific/Technology /p h3All Job Posting Locations /h3 ulliSchaffhausen, Switzerland /li /ul h3Job Description /h3 pSenior Engineer, MSAT Biotherapeutic Drug Product (PG26) /p h3About Innovative Medicine /h3 pOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at /p pWe are searching for the best talent for Senior Engineer, MSAT Biotherapeutic Drug Product (DP)!

This hybrid position will be located in Schaffhausen, Switzerland. /p h3Responsibilities /h3 ul liServe as Site Technical Owner for NPI, Tech Transfer Projects, and specific commercial products /li liServe as Subject Matter Expert for Optical inspection related processes, e.g.