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Purpose of your Job

As a Client Project Manager, you will play a central role in managing client interactions and coordinating with internal teams. Your responsibility is to ensure that drug product development projects progress smoothly, meeting agreed timelines and budgets while maintaining a high level of scientific and strategic insight. You will act as the key link between our clients, the technical teams, and the commercial unit. In this role, you will provide technical guidance to our clients and collaborate closely with internal experts to drive successful project outcomes.

Join Coriolis Pharma – a science-driven service provider shaping the future of biopharmaceutical drug products!

Your Responsibility

• Manage multiple client projects (number depending on complexity) from post-sales kick-off to completion.
• Lead regular project meetings with internal teams and clients (mostly virtual; occasional travel for key milestones).
• Ensure project timelines, deliverables, and financial frameworks are met.
• Act as a point of contact for client questions, change requests, and escalations.
• Coordinate closely with Business Development, Account Management, and Operational Teams.
• Support preparation of project amendments or change orders during ongoing collaborations.
• Offer guidance to clients based on your understanding of drug product development and analytical services.

What you need to succeed

• A Master’s degree (or equivalent qualification) in a relevant scientific or business field is required; a PhD is preferred
• Solid understanding of drug product development for parenteral biopharmaceuticals, including formulation and analytical aspects
• Relevant experience in the pharmaceutical or biotech industry, with a strong track record in client-facing project management, and a solid understanding of project management methodologies (e.g., Agile, Waterfall; PMP or PRINCE2 certification is a plus)
• Up-to-date knowledge of regulatory expectations and quality standards, including ICH guidelines (e.g., Q5A, Q8-11, etc.), GMP, GLP, and EMA/FDA requirements relevant to parenteral biopharmaceuticals
• Strong communication and organizational skills, with experience in scientific or technical project environments
• Fluent English skills (spoken and written); German is a plus
• Proficiency with project management and digital collaboration tools, including CRM systems, project management software (e.g., MS Project, Asana, BCS, or similar), Microsoft Office applications, and ERP systems
• Availability to work onsite in Martinsried (partial remote-work possible)
• Flexibility to travel (if required by projects/clients)