10 дней назад
MSAT Site Lead Synthetics Schaffhausen (Pharmaceutical Manufacturing)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
MSAT Site Lead Synthetics Schaffhausen (Pharmaceutical Manufacturing): Leading technical operations and the MSAT team for synthetic drug substance and solid oral drug product manufacturing with an accent on technology transfer, lifecycle management, validation, compliance, and supply reliability. Focus on developing people, solving complex process and quality issues, strengthening process capability, and deploying analytics, PAT, automation, and continuous improvement.
Location: Based in Schaffhausen, Switzerland; up to approximately 10% domestic and international travel.
Company
Johnson & Johnson MedTech develops healthcare and medical technology solutions across the spectrum of healthcare.
What you will do
- Lead and develop the Schaffhausen MSAT team, setting priorities, deploying resources, and translating global and site strategies into local objectives.
- Own technical support for synthetic drug substance and solid oral drug product portfolios, including process monitoring, troubleshooting, risk assessment, and lifecycle improvement.
- Lead product introductions, scale-up activities, technology transfers, major changes, fit-to-plant assessments, documentation, and validation.
- Partner with Operations and Value Chain teams to improve process capability, yield, capacity, cost, and supply resilience.
- Govern process validation, cleaning validation, continued verification, investigations, CAPAs, and inspection or audit readiness.
- Drive standardization, lean practices, data analytics, PAT, automation, capital project support, and technology deployment.
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 synthetic drug substance and solid oral drug product processes, including their interdependencies.
- Experience with technology transfer, lifecycle management, process or cleaning validation, and continued process verification.
- Strong knowledge of GMP, regulatory expectations, quality systems, process safety, EH&S, and related compliance requirements.
- Fluent English and German required, together with demonstrated people and change leadership in a global matrix organization.
Nice to have
- Leadership of multidisciplinary teams supporting both Drug Substance and Drug Product operations.
- Experience with inspections, capital projects, advanced manufacturing technologies, data analytics, and lean principles.
- Ability to build effective internal and external partnerships.
Culture & Benefits
- Inclusive work environment grounded in integrity, accountability, and respect for individual contributions.
- Global and site-level collaboration across MSAT, Operations, Quality, Value Chain, and subject-matter expert networks.
- Opportunity to improve manufacturing robustness, sustainability, speed, cost, and competitiveness.
- Domestic and international travel of up to approximately 10% is expected.
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