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.
Technical Project Manager – Pre-Filled Syringes (m/f/d)
Your role
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.
Ihr Profil:
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.
Working at Siegfried
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.
Who we are
In the Midst of People’s Lives – Across the Globe
The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model.
The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production.
We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products
What we do in Hameln
Hameln is a renowned contract manufacturer which supplies both national and international pharmaceutical companies. It has over 450 employees who produce sterile medicinal products, mainly for use in hospitals and intensive care facilities.
Main activities
Contract manufacture of parenteral solutions and suspensions – aseptic or terminally sterilized in ampoules and vials
Specialist in the production of complex preparations such as anesthetics, flammable and oxygen-sensitive liquids and cold chain products
Special features
Successful transfers and establishment of new products in sterile production
Batch size: up to 3500 liters
Clean room area: 4000 m²
Batch manufacture and filling of sterile products, from visual inspection through to final packaging
Strategic importance
Contract manufacturing for parenterals
Apply now
