Head of Operations

At MYNERVA – a Wyss Zurich project – our mission is to improve the lives of individuals suffering from neuropathy. MYNERVA has developed a medical device to artificially restore the sense of touch and decrease pain using non-invasive neurostimulation.

We are seeking a highly driven Head of Operations (100%) to lead our operational infrastructure, regulatory strategy, and quality systems as we prepare for clinical and commercial scale-up. This role is ideal for an experienced leader with a strong track record in operations, medical device compliance, and international market readiness, particularly in the United States.

The Head of Operations will be responsible for overseeing the full operational backbone of MYNERVA, including project management, supply chain, manufacturing, quality, and regulatory affairs. This individual will be part oft he leadership team and collaborate closely with the executive team to build scalable processes and ensure that our products production and delivery meet the highest standards. The position is based in Zurich (100% on site).

• Operations
  • Lead operational planning and execution with clear KPIs, timelines, and budgetary controls in cordiantion with other departments.
  • Drive continuous improvement across operational workflows, cost control, and risk management.
• Manufacturing & Supply Chain Management
  • Set up and manage scalable manufacturing operations (including supplier management) to support clinical and commercial needs.
  • Oversee procurement, production planning, and inventory management to ensure on-time delivery and quality.
  • Monitor and optimize logistics and global distribution strategies.
• Quality & Regulatory
  • Guide quality team in implementing a robust quality management systems in accordance with ISO 13485, FDA QSR (21 CFR 820), and related standards.
  • Support and execution of regulatory strategy for the US (FDA) and international markets in collaboration with the CEO, regulatory team and external consuntants.
  • Support the regulatory submission process together with internal resources and consultants.

• Education & Experience:
  • Bachelor’s or Master’s degree in Engineering, Operations, Quality, or a related field.
  • Minimum 10 years of industry experience, with at least 5 years in operations roles within the medical device industry.
  • Proven experience with US FDA regulatory pathways and commercializing products in the US market.
• Skills & Competencies:
  • High energy and well-organized individual with hands on approach.
  • Strong entrepreneurial approach.
  • Strong understanding of medical device manufacturing and quality requirements.
  • Strategic thinker with excellent execution, leadership, and organizational skills.
  • Understanding of international regulatory frameworks (FDA, ISO 13485).
  • Familiarity with risk management, document control, and design controls.
  • Strong communication and stakeholder management skills.
  • Fluency in English (German or other languages are a plus).

• A high-impact role in a cutting-edge MedTech startup.
• Fast-track career growth opportunities as MYNERVA scales.
• A highly motivated and collaborative team dedicated to improving patients’ lives.
• A dynamic, diversified, and innovation-driven work environment.
• Benefits according to ETH Zurich’s employee benefits program.

We look forward to receiving your online application with the following documents:

• Video pitch introduction (compulsory, 1 min max)
• CV
• Motivation letter: why MYNERVA?
• Reference letters

Please note that we exclusively accept applications submitted through our online application portal. Applications via email or postal services will not be considered.

Further information about MYNERVA can be found on our website . For further questions, do not hesitate to reach out to Greta Preatoni (Write an email).

We would like to point out that the pre-selection is carried out by the responsible recruiters and not by artificial intelligence.

For recruitment services the  GTC of ETH Zurich   apply.