Project Manager - Clinical Products (m|f|d)

Project Manager – Clinical Products (m|f|d)

Company Description
For 35 years, we have been developing cutting-edge science and technology to empower biomedical research and personalized medicine. We combine excellence from more than 60 disciplines in natural sciences, engineering, and informatics to make a significant contribution to biomedical sciences. We encourage a creative working environment driven by pioneering spirit – to seek new horizons – boldly envisioning the future and turning it into reality. Today, more than 4,700 experts from over 50 countries contribute to our sustainable success.
Job Description
Your role

• Within the Clinical Products department, you play a key role in initiating, planning, monitoring, and managing projects related to pharmaceutical production and supply chain processes. This includes updating existing production processes, further developing GMP-compliant workflows, and implementing initiatives to enhance production safety.
• In a rapidly growing environment, you analyze, design, and optimize operational procedures to improve efficiency and quality.
• You take full responsibility for assigned projects and/or sub-projects and lead cross-functional project teams.
• Together with your team, you translate project requirements into comprehensive and goal-oriented solutions – always aligned with the company\’s overall objectives.
• Throughout project execution, you ensure compliance with applicable standards and regulations (e.g. GMP) and collaborate closely with departments such as Production, Business Development, R&D, Quality Control, Quality Assurance, Regulatory Affairs, Marketing, and Procurement.

Qualifications
Your profile

• You hold a degree in biotechnology, biopharmaceuticals, or a related field within the life sciences.
• You bring solid expertise in the field of medical devices, pharmaceuticals, or cellular immunotherapy.
• Ideally, you have practical experience in clinical manufacturing or in the development of mRNA-based products and nanoparticles.
• You are familiar with the documentation of standards and regulatory requirements of a GMP-compliant environment.
• You communicate clearly and confidently, work proactively, and are fluent in both written and spoken English.

Additional Information
What we offer

• Flexible and remote work: Enable time management on your terms
• Diversity: International teams and cross-border intercultural communication
• Room for creativity: It\’s the most clever solution that we always strive for
• Health & Sport: We offer a wide range of corporate sports activities and health provision
• Miltenyi University: A clever mind never stops learning, take advantage of our in-house Training Academy

Diversity is the bedrock of our creativity.
Our mission: To innovate treatments and technologies and tackle the world\’s most serious health challenges. And that\’s why we connect the dots -across various disciplines, linking different perspectives, skills, and abilities.
You and your talent are welcome here in our inclusive and collaborative environment. So come as you are. Regardless of gender, sexual identity, age, ethnicity, religion or disability.
Become part of our team and focus on pushing the borders of medicine.
Contact us
If you have the skills and qualifications for this position, please use the link to send us your details (application letter, curriculum vitae, references and certificates). Please give us some idea of when you can start and the kind of salary you are looking for.

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