How you match

Skills

Developing OthersProcess engineeringCrisis managementInclusive Leadership TrainingEmerging technologies implementationTechnical program managementProject SchedulingAdministrative process improvementNorms and Manufacturing ProcessesLean LeadershipProcess ManagementTarget Costing

Languages

EnglishGerman

The role

MSAT Site Lead, Synthetics Drug Substance & Drug Product (Schaffhausen)

01Lead and develop the Schaffhausen MSAT team, setting priorities and deploying resources effectively.

02Translate global MSAT, Synthetics platform, and site strategies into measurable local objectives, governance, and risk management.

03Provide the technical voice in site and global leadership forums and promote an end-to-end DS–DP approach through shared standards and knowledge.

04Own technical support for the commercial portfolio, including process monitoring, troubleshooting, risk assessment, and lifecycle improvement.

05Lead new product introductions, scale-up, transfers, and major changes, including fit-to-plant assessment, documentation, validation, and cross-functional governance.

06Partner with Operations and Value Chain teams to improve process capability, yield, capacity, cost, and supply resilience.

07Lead or support complex investigations, ensuring robust root-cause analysis, effective CAPAs, and organizational learning.

08Provide governance for process validation, cleaning validation, continued verification, and applicable MSAT content in the Site Validation Master Plan.

09Support health authority inspections and internal or customer audits; serve as MSAT presenter or lead for relevant processes and technical topics.

10Drive process excellence through standardization, lean practices, data analytics, PAT, automation, and other fit-for-purpose technologies.

Requirements

↳Bachelor’s degree or equivalent in Chemical Engineering, Chemistry, Pharmaceutical Sciences, or a related discipline; an advanced degree is preferred.

↳At least 8 years of relevant pharmaceutical manufacturing, process development, technical operations, or MSAT experience.

↳Strong knowledge of Synthetics Drug Substance and solid oral Drug Product processes and DS–DP interdependencies.

↳Experience in technology transfer, lifecycle management, process or cleaning validation, and continued process verification.

↳Strong knowledge of GMP, regulatory expectations, quality systems, process safety, and EH&S.

↳Demonstrated people and change leadership in a global matrix organization.

↳Strong analytical, problem-solving, project, resource, stakeholder, and business-management skills.

↳Excellent communication, influencing, and negotiation skills.

Benefits

Tech stack

Data analyticsLean practicesAutomationProcess validationCleaning validation

Company

Johnson & Johnson / Janssen

Pharmaceuticals

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 jnj.com . As 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.

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