Group Leader (f/m/d) – GMP Analytical Service Group

Coriolis Pharma Research GmbH

82152 Planegg - Deutschland

Gruppen-, Teamleiter/in Vollzeit ab 04.11.2025

Beschreibung

### Purpose of your Job

As a Group Leader in our GMP Analytical Service Group at Coriolis Pharma, you will take on a key leadership role in managing a team of scientists dedicated to the analytical characterization of biopharmaceutical drug products. Your focus will be on delivering high-quality, GMP-compliant analytical services, including method development, validation, and routine testing.
You will be responsible for ensuring the smooth execution of client projects, maintaining regulatory excellence, and driving innovation within a highly regulated environment. Acting as a strategic and operational leader, you will guide your team, collaborate with internal stakeholders, and contribute to the continuous improvement of our analytical capabilities.

### Your Responsibility

Leadership & People Development:

- Lead a team of motivated scientists focused on GMP-compliant analytical characterization of biopharmaceutical molecules
- Develop and implement a strategic plan for team growth, including recruitment and onboarding of new talent
- Drive career development through structured performance reviews, feedback, and individual development plans
- Act as the disciplinary manager for your team members

Operational & Business Accountability:

- Responsible for the group’s sales and revenue targets
- Ensure operational excellence and timely execution of client projects
- Manage team resources effectively, including capacity planning and KPI tracking
- Foster strong collaboration with internal stakeholders (e.g., Quality, Commercial, Finance, Technical Support)
- Promote innovation and maintain cutting-edge scientific and regulatory expertise in GMP-compliant analytical services
- Drive continuous improvement through process optimization and implementation of robust, scalable workflows
- Ensure full compliance with applicable quality and regulatory standards

### What you need to succeed

- Master’s degree or equivalent in (bio)chemistry, biology, pharmacy, medical sciences, or a related field; PhD is a strong advantage
- Minimum 6 years of professional experience, including at least 3 years in a leadership role within a GMP-regulated environment
- Proven expertise in GMP analytical method development, validation, characterization, and tech transfer for biopharmaceutical drug products
- Deep understanding of regulatory standards and method lifecycle management
- Strong business and project management skills, including strategic thinking, resource planning, prioritization, and risk management
- Inspirational leadership style with a hands-on mentality and openness to innovation
- Team-oriented with excellent interpersonal and communication skills
- Fluent in German and English, both written and spoken

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