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

Stellenbeschreibung:

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

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.

This is a fixed-term (18 months) position. 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.

Responsibilities

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.
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.