(Technical) Project Manager (f/m/d) - GMP

Permanent employee, Full or part-time · Martinsried (BY)

Purpose of your Job

At Coriolis Pharma, we are committed to ensuring the successful production and commercialization of our clients' biopharmaceutical products. As a GMP Project Manager, you will leverage your scientific expertise and project leadership skills to manage operative customer projects in the GMP-regulated environment. You will oversee the execution of laboratory operations and will be ensuring that scientific objectives are met within quality and regulatory frameworks.

Your Responsibility

As a GMP Project Manager, you will manage the execution of customer projects, coordinate laboratory activities, and ensure compliance with project requirements. Your responsibilities will include:

Take over the responsibility to lead and manage drug product development or Analytical projects under GMP
Take over the lead in the communication with the client from technical end and coordinate internally with other project team members and involved units at Coriolis
Ensure that relevant resources are embedded into the project and that project-related decisions are based on state-of-the-art scientific principles
Perform experimental project planning, coordination, resource management, and execution (supported by project team members)
Ensure that project deliverables, i.e. experimental plans, experimental data, data presentations and reports are prepared timely and according to the required quality standards
Take over the responsibility for interpretation of scientific data and the drawing of final conclusions; compile and present scientific data presentations as well as technical reports
Equipment & Compliance Management: Oversee the qualification, maintenance, and proper functioning of analytical equipment, ensuring compliance with GMP standards. Manage equipment calibration, validation, and maintenance activities, ensuring that all systems meet regulatory requirements.
Quality Assurance & Regulatory Compliance: Lead efforts to ensure full adherence to QA and QC processes. Manage deviations, CAPAs, change controls, and out-of-specification (OOS) results, ensuring that all actions align with regulatory guidelines.

What you need to succeed

A degree in pharmacy, (bio)chemistry, biotechnology, biophysics, or a related field (PhD preferred).
Proven experience in managing large-scale projects and leading of project teams
Ability to simplify and reduce complex tasks into the key elements.
Flexibility in working in different environments (GMP and R&D) as well as willingness to work across time zones
In-depth understanding of GMP regulations, quality management systems, and regulatory standards.
Practical experience in a GMP-regulated laboratory environment, with expertise in laboratory techniques such as HPLC, UV-Vis spectroscopy, and particle size analysis is preferred.
Strong background in analytical method development, validation, and qualification.
Strong communication skills in English, both written and verbal, and the ability to collaborate effectively with cross-functional teams and clients.

Why to join Coriolis?

Let’s formulate innovation together…
Our success & development is created by the people working together @Coriolis.
We put People first! That’s why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and clients.

We would like to grow together with you!
Let’s continue building and creating the future now, join our team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience.
We offer an attractive work space at the Martinsried site. Let’s make a difference together!

Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, sex, citizenship or gender identity, color, disability, religion/belief, sexual orientation, marital status, age or individual preferencies. Different backgrounds, experiences and ideas push us further and raise the bar.

Thank you for your interest! We look forward to receiving your application documents.
Please use our career portal exclusively for this purpose.
We would like to support you from the very beginning to shape your development possibilities here at Coriolis.
For questions or further information, please visit our website or contact us directly.

We are looking forward to your application!

Your Contact

Dominik Schwemmer
Senior Business Partner - Talent & Development
People, Organization & Culture Unit

Coriolis Pharma Research GmbH
Phone: +49 (0) 89 – 417760 - 0
Fraunhoferstraße 18 b, 82152 Martinsried
www.coriolis-pharma.com

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About us

Coriolis Pharma, is a globally operating service provider and one of the world leaders in formulation research and development of (bio)pharmaceutical drugs and vaccines.
We revolutionize the development process of biopharmaceutical drugs by integrating innovative digital formulation approaches from drug development to commercial products.

As a people and team-oriented company with an interdisciplinary team of highly skilled scientists and an expert scientific advisory board, we provide cutting-edge services and tailor-made solutions for our clients.

Our company culture is based on diversity, teamwork and open and appreciative communication. That's why wonderful people from over 35 nations around the world work together successfully at Coriolis.

What motivates us? Our motivation is to enable the development of innovative drugs by performing outstanding biopharmaceutical research to improve the quality of life for humankind.

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Your application!

We appreciate your interest in Coriolis Pharma Research GmbH. Please fill in the following short form.
Should you have any difficulties in uploading your files, please contact us by mail at career@coriolis-pharma.com.