Job Description
Are you ready to shape the future of pharmaceutical manufacturing and the CDMO industry?
We are in search of an aspiring Technical Project Manager to join our world-class team. This is a unique opportunity for an expert in pre-filled syringe technology to take their career to the next level, leading transformational projects that shape the future of healthcare.
In this strategically important role, you will be at the forefront of further developing and industrializing state-of-the-art pre-filled syringe capabilities. As part of the site leadership team, you partner closely with cross-functional teams to deliver projects from R/D to full-scale commercial manufacturing, ensuring the highest standards of quality and efficiency.
This role also provides the opportunity to contribute to a global organization, sharing your knowledge and expertise across sites. Apply now to shape the future of pharmaceutical manufacturing!
For our company we are looking for employees from the regions of Hamel, Hannover, Bielefeld, Göttingen, Paderborn, Berlin, Bremen, Hamburg, Münster and Osnabrück.
This pivotal role combines deep leadership with technical expertise, innovation, and global collaboration.
Leadership and Innovation
- Lead the end-to-end development of pre-filled syringe technologies, including formulation, filling processes, and device assembly.
- Champion innovation in PFS product design and manufacturing processes, ensuring scalability and robustness.
- Act as the organization's subject matter expert for pre-filled syringe technologies, driving knowledge sharing and collaboration.
- Manage projects from R&D through to commercial-scale manufacturing, ensuring milestones are met on time and within budget.
- Guide the tech transfer of pre-filled syringe products, ensuring seamless scale-up and integration into manufacturing sites.
- Partner with cross-functional teams, including scientists, engineers, and regulatory experts, to ensure product success.
Process Optimization and Troubleshooting
- Design and optimize processes to achieve excellence in quality, efficiency, and compliance.
- Solve complex technical challenges, leveraging your expertise to ensure reliable manufacturing outcomes.
Regulatory and Compliance
- Assure full compliance with GMP and regulatory standards throughout development and manufacturing.
- Contribute to the preparation of technical documentation for regulatory submissions and audits.
Global Collaboration
- Work with teams across the globe, contributing to and learning from a global network of experts.
- Travel internationally to provide on-site support for projects, training, and technical troubleshooting.
- A minimum of 7+ years of hands-on experience in pre-filled syringe technology, from development to commercial manufacturing.
- A proven track record of successfully bringing pre-filled syringe products to market.
- Strong experience in tech transfer and managing large-scale projects.
Education and Background:
- A degree in Pharmacy, Engineering, Process Engineering, or a related field. Advanced degrees (Master's or PhD) are highly desirable.
Technical Expertise:
- Expertise in troubleshooting, process optimization, and scaling up PFS technologies.
- Familiarity with regulatory and quality standards specific to pre-filled syringes.
Leadership and Communication:
- Strong leadership skills, with the ability to inspire and guide cross-functional teams.
- Excellent communication skills to articulate technical concepts to diverse stakeholders.
- Additional performance-based remuneration ("Short-Term Incentive").
- Working hours: 37.5 hours/week.
- 30 vacation days and additional leave.
- Employee discounts, e.g., at local fitness studios.
- On-site occupational health services.
- Free parking spaces and good public transport connections.