Technical Project Manager - Pre-Filled Syringes (m/f/d)

Stryker Corporation; Hameln; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

An innovative company is seeking a Technical Project Manager to lead transformative projects in pre-filled syringe technology. This role offers the opportunity to shape the future of healthcare by developing and industrializing cutting-edge capabilities. You will collaborate with cross-functional teams to ensure project success while adhering to the highest quality standards. Join a global organization where your expertise will drive impactful changes in pharmaceutical manufacturing. If you are ready to take your career to the next level, this is the perfect opportunity for you.

Leistungen

Performance-based remuneration

30 vacation days

Employee discounts

On-site occupational health services

Free parking

Good public transport connections

Qualifikationen

• 7+ years of experience in pre-filled syringe technology.
• Proven track record in managing large-scale projects.

Aufgaben

• Lead development of pre-filled syringe technologies.
• Manage projects from R&D to commercial-scale manufacturing.

Kenntnisse

Pre-filled syringe technology

Project management

Process optimization

Regulatory compliance

Technical troubleshooting

Ausbildung

Degree in Pharmacy

Degree in Engineering

Advanced degrees (Master's or PhD)

Jobbeschreibung

General Information

Country Germany

City Hameln

Functional Area Research & Development

Job Group Project Management

Employment Type Permanent Contract

Working time Full-time

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!

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.

Project Execution

• 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.

Your profile

Experience:

• 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