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Method Development
vor 2 Wochen
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 (MD&V) 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.
- First experience in leading a team and managing complex analytical projects is an advantage.
- 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
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.