Senior Director, Global Quality Operations - Switzerland

About the role

This role leads global quality operations for clinical and commercial products, overseeing CMOs and external partners across intermediates, drug substance, drug product, and finished goods to ensure supply and regulatory compliance. This role sets global quality operations strategy, resolves issues, strengthens quality systems, and builds team capability to support business and pipeline needs. This role oversees quality operations for imports, market release, wholesale distribution, and safe trading of medicinal products. This role ensures phase-appropriate GMP/GDP quality assurance across all relevant territories including but not limited to US, the EU/EEA, and Australia, ensuring products are manufactured, released, and distributed in line with regulations and company procedures. The role builds country quality functions and regional structures to support product release, commercial strategy, and launches. The role serves as a liaison between international affiliates and Apellis Pharmaceuticals Inc., ensuring alignment with the global quality system and local requirements. The role oversees routine GMP batch production for intermediates, drug substance, and drug product managed under Apellis Inc and Apellis International GmbH. The role may train and qualify staff and delegate tasks as needed. Roles and Responsibilities: Provides strategic and operational oversight to ensure timely market release, reliable supply, and safe trading of high-quality medicinal products, including direct technical supervision of GxP activities. Serves as the Quality GxP Lead and acts as Apellis' senior Quality leader for the international region, defining strategy and supporting continued global growth and expansion. Develops and leads the international Quality organization in close alignment with Global Quality, including build-out of affiliate quality structures and oversight of global quality operations supported by a unified GMP/GDP QMS. Ensure implementation, maintenance, and continuous improvement of the Quality Management System, including risk identification, escalation of critical quality issues (e.g., complaints, recalls, counterfeits), and inspection readiness. Maintains end-to-end GMP/GDP oversight of intermediates, drug substance, and drug product under Apellis Inc and Apellis International titles, ensuring compliant manufacturing, certification, release, storage, distribution, and full batch traceability. Oversee qualification, management, and auditing of Contract Manufacturing Organizations (CMOs) and Contract Service Providers (CSPs), including establishment of quality agreements and periodic requalification. Ensures appropriate controls for product handling and distribution, including validated storage conditions, and investigation of deviations such as temperature excursions and security breaches, with regulatory notification as required. Leads batch certification and release activities, ensuring required documentation (e.g., CoA) is reviewed, approved, and archived, and that only compliant batches are released. Represents Quality in inspections and audits, supports vendor audit programs, and ensures effective self-inspection and Quality Management Review processes. Collaborates cross-functionally with Regulatory, Supply Chain, and other stakeholders to support business objectives and product lifecycle activities.

Requirements

• Education, Registration, Advance Training &/or Certifications:
• Master's degree in science or pharmacy
• Experience, Expert Knowledge &/or Competencies:
• In-depth knowledge of applicable regulations and guidelines, including but not limited to 21 CFR 11, 210, 211, Swiss Medicinal Products Licensing Ordinance (SR 812.212.1), EU GMP (EudraLex Volume 4; notably Annexes 1, 13, and 16), and GDP requirements for medicinal products and active substances.
• Strong expertise in U.S., European and international regulatory frameworks, ensuring full compliance across import, export, and foreign trade activities, including end-to-end supply chain adherence to GDP requirements.
• Extensive experience in batch disposition and certification, including importation into the EU.
• Proven leadership in Quality Systems management, including inspection readiness and global QMS alignment.
• Demonstrated expertise in deviation and non-conformance management, including root cause analysis and CAPA implementation.
• Track record in driving systematic process improvements and continuous quality enhancement initiatives.
• Experience & Competencies
• Leadership & Organizational Development: Proven ability to lead and develop high-performing, diverse teams, effectively navigating different working styles and driving collaboration across a global matrix organization.
• Strategic & Operational Leadership: Defines and executes aligned quality strategies, gaining commitment from internal and

Benefits

Additional Information

Opportunity awaits those up to the challenge of developing transformative therapies across a broad range of debilitating diseases.

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