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Vice president (vp), advanced materials manufacturing - switzerland

Hünenberg
Hotel du Parc
EUR 175’000 pro Jahr
Inserat online seit: 5 Mai
Beschreibung

Vice President (VP), Advanced Materials Manufacturing - Switzerland

We are a globally emerging company operating at the intersection of advanced materials science and human health. We are transferring a highly complex, vertically‑integrated manufacturing capability from East Asia to Europe, with Switzerland as the chosen base. This greenfield build is a strategic move to regionalise supply chains and establish sovereign manufacturing capability within core markets.


Key Responsibilities

* Site Establishment & Manufacturing Leadership
o Lead all aspects of greenfield site development: location assessment, infrastructure build‑out, equipment qualification, and operational ramp‑up
o Develop and execute the long‑term manufacturing strategy aligned with global supply requirements and capacity roadmap
o Establish production planning, scheduling, and resource frameworks to meet commercial targets from first production
o Drive technology integration, automation, and digital manufacturing initiatives from day one
o Set and enforce the highest standards of operational discipline, workplace safety, and environmental sustainability
* Quality Systems & Compliance
o Design and implement a world‑class quality management system compliant with applicable international standards and the Swiss regulatory framework (Swissmedic)
o Establish all SOPs, documentation architecture, and quality controls for in‑process and finished material release
o Lead root‑cause analysis, CAPA, and quality risk management disciplines across all operations
o Oversee supplier qualification and ongoing supply quality management
* Regulatory Affairs
o Develop and execute the regulatory strategy to achieve and maintain compliance with Swiss, European, and international requirements applicable to precision‑manufactured materials
o Lead engagement with Swiss and European regulatory authorities throughout the site establishment and certification process
o Oversee preparation of technical documentation, regulatory submissions, and all authority‑facing deliverables
o Monitor the evolving international regulatory landscape and ensure timely implementation within site operations
* Cross‑Functional & Executive Leadership
o Build, lead, and develop the manufacturing, quality, and regulatory functions — attracting and retaining talent in a greenfield context
o Partner with R&D, global supply chain, commercial, and finance leadership to align site capabilities with business priorities
o Represent the site at group executive level and contribute to global strategic planning
o Champion a culture of scientific rigour, accountability, and continuous improvement
* Performance & Financial Management
o Define and manage KPIs across manufacturing performance, quality outcomes, and regulatory compliance
o Hold full P&L accountability for the site, ensuring cost discipline and budget adherence
o Maintain compliance with all EHS regulations applicable to the manufacturing environment


Candidate Profile

* Academic Background
o Advanced degree in Engineering, Chemistry, Materials Science, Biotechnology, or a cognate discipline
* Experience
o Minimum 20 years in senior manufacturing leadership roles within highly regulated production environments, with progression to VP or equivalent executive accountability including full P&L and regulatory responsibility
o Hands‑on experience establishing a greenfield regulated manufacturing facility— from site selection and authority engagement through GMP or equivalent certification to full operational ramp‑up; preference for raw or specialty materials
o Accountability for quality assurance, quality control, and regulatory affairs functions at an enterprise or global level
o Success in managing regulatory inspections and certification processes with multiple international authorities
o Experience operating within or alongside the Swiss regulatory environment (Swissmedic) and familiarity with European frameworks
o Significant experience navigating the Chinese regulatory landscape, including engagement with the NMPA and provincial authorities— a non‑negotiable requirement
o Experience managing and qualifying Asian‑based supply chain partners at an operational and quality level
* Languages
o Full professional fluency in English – required
o Native‑level Mandarin Chinese – required


Location & Engagement

* Location: Switzerland (site location to be determined; accessibility for supply‑chain logistics is a key consideration in the ongoing site assessment)
* Reporting: Group C‑Suite
* Engagement: Exclusive retained mandate; candidates and enquiries are treated in strict confidence


Employment Details

* Employment start: Immediately
* Employment duration: Permanent
* Workload: 100%
* Salary: Not disclosed
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