Head of Operations Clinical Bioconjugation (Biopharmaceutical Manufacturing)
Контакты
Формат работы
onsite
Тип работы
fulltime
Грейд
head
Английский
c1
Страна
Switzerland
six sigmaprocess optimizationautomationgmplean manufacturingoperational leadershipquality compliancecapital investmentbiopharmaceutical manufacturing
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Сильная вакансия
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Чётко описанная руководящая роль в крупной компании в сфере наук о жизни даёт значительный масштаб влияния в специализированном биофармацевтическом направлении, но ответственность за организацию из 400-500 человек будет высокой.
?Масштабное руководство
Чёткая зона ответственности
Перспективное направление
Ресурсы крупной компании
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Head of Operations Clinical Bioconjugation (Biopharmaceutical Manufacturing): Leading a 400–500-employee clinical bioconjugation manufacturing unit with an accent on operational performance, GMP compliance, quality, safety, customer delivery, financial efficiency, and asset management. Focus on translating business strategy into operational excellence, developing multidisciplinary leadership teams, and driving Lean, automation, process optimization, and sustainable growth.
Location: Visp, Switzerland
Company
hirify.global is a global life sciences company operating across five continents and providing biopharmaceutical manufacturing products and services.
What you will do
Lead a dedicated 400–500-employee manufacturing unit within the Visp site with end-to-end accountability for performance, safety, quality, compliance, delivery, financial efficiency, and asset management.
Define and execute operational strategies covering capacity, productivity, workforce planning, and resource allocation.
Drive production performance, reliability, right-first-time execution, continuous improvement, Lean methodologies, automation, and process optimization.
Own operational budgets and controllable costs, manage asset lifecycle strategies, and sponsor capital investments.
Develop and empower a multidisciplinary leadership team, including talent development and succession planning.
Collaborate with Quality, Engineering, MSAT, Supply Chain, Project Management, site leadership, customers, auditors, and regulatory stakeholders.
Requirements
Bachelor’s or Master’s degree in Chemical Engineering, Pharmaceutical Technology, Chemistry, Biochemistry, Biotechnology, or a related scientific or engineering discipline.
10+ years of experience in pharmaceutical or biopharmaceutical manufacturing operations, ideally in drug substance manufacturing, with exposure to process development and technology transfer.
Strong understanding of GMP manufacturing, regulatory compliance, operational excellence, and manufacturing performance management.
Experience managing significant operational budgets, capital investments, asset strategies, and organizational transformation.
Strong business acumen, strategic thinking, and ability to translate operational priorities into measurable business outcomes.
Exceptional leadership, communication, and stakeholder-management skills, with the ability to develop high-performing teams and influence across functions.
Fluent English required.
Nice to have
An MBA or Executive MBA.
Experience implementing Lean Manufacturing, Six Sigma, automation, or continuous improvement initiatives.
German language skills.
Culture & Benefits
Leadership position within a Site-in-Site manufacturing operation at a key biopharmaceutical manufacturing location.
Operational ownership combined with the infrastructure, governance, and shared services of the wider Visp site.
Opportunity to shape the future of Clinical Bioconjugation manufacturing and drive sustainable growth.
Commitment to ethical business results, employee protection, environmental responsibility, and equal opportunity.
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