Method Development & Validation Manager

Our client is a dynamic GMP-certified service laboratory specializing in analytical testing, method development, and validation for generics and nutritional supplements.

Their focus is scientific excellence, quality, and customer satisfaction delivered by a passionate, collaborative team. To strengthen the organization, they are looking for an experienced and motivated Method Development & Validation Manager to lead the analytical development team and drive innovation and quality across all projects.

Method Development & Validation Manager

As the MD&V Manager, you will be responsible for the scientific, operational, and strategic management of the Method Development & Validation (MD&V) department.

Your Responsibilities:

• Lead and develop a team of analytical scientists and project leads.
• Plan and oversee method development, validation, and transfer projects according to GMP and ICH guidelines.
• Ensure scientific excellence, regulatory compliance, and timely project execution.
• Review and approve protocols, reports, and technical documentation.
• Act as primary scientific contact for clients and support business development with technical expertise.
• Collaborate closely with QA and QC departments to ensure seamless process integration.
• Identify and implement process improvements and new analytical technologies.
• Manage departmental resources, budget, and training programs.
• Represent the MD&V department during audits and inspections.
• Ensure that health and safety guidelines and safe working practices are followed.
• Contribute to the setup of new quality standards for nutritional supplements.
• Give presentations both at internal meetings and externally at conferences.

Your qualifications

• MSc in Analytical Chemistry, Pharmaceutical Sciences, or a related field is desired.
• Several years of experience in analytical development, validation, or QC within a GMP-regulated environment.
• Proven experience in leading teams and managing complex analytical projects.
• Strong understanding of regulatory guidelines (ICH Q2, GMP, Ph. Eur., USP).
• Hands on expertise with instrumental techniques (e.g., HPLC, GC, LC-MS, Dissolution, ICP-OES).
• Strong organizational skills in a results driven environment, with a strong customer focus and the ability to remain flexible under changing priorities and tight deadlines.
• Analytical and strategic mindset with a solution-oriented approach.
• High sense of responsibility, quality awareness, and integrity.
• Culturally sensitive and enjoying working in international teams.
• Excellent communication skills, both written and verbal in English and German.

Your application

Please apply online. For further information about the position, please contact your Gi Consultant, Ms. Marta Castellano, MSc Biology (+41 76 342 57 90).

Gi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world.