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

Siegfried

Hameln

Vor Ort

EUR 70.000 - 90.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

A leading company in pharmaceutical manufacturing is seeking a Technical Project Manager to lead projects in pre-filled syringe technology. This role involves overseeing development, ensuring compliance, and collaborating globally to drive innovation and efficiency in manufacturing processes.

Leistungen

Performance-based incentives
30 vacation days
Employee discounts
Health services
Parking access
Public transport access

Qualifikationen

  • 7+ years of experience in pre-filled syringe technology.
  • Proven success in bringing pre-filled syringe products to market.

Aufgaben

  • Lead development of pre-filled syringe technologies.
  • Manage projects from R&D to commercial manufacturing.
  • Ensure compliance with GMP and regulatory standards.

Kenntnisse

Leadership
Communication
Troubleshooting
Process Optimization

Ausbildung

Degree in Pharmacy
Degree in Engineering

Jobbeschreibung

Are you ready to shape the future of pharmaceutical manufacturing and the CDMO industry?

We are seeking an aspiring Technical Project Manager to join our world-class team. This role offers a unique opportunity for an expert in pre-filled syringe technology to advance their career by leading transformational projects that influence healthcare's future.

In this strategic position, you will develop and industrialize advanced pre-filled syringe capabilities. As part of the site leadership team, you will collaborate with cross-functional teams to deliver projects from R&D to full-scale commercial manufacturing, maintaining high standards of quality and efficiency.

This role also allows you to contribute to a global organization, sharing your expertise across multiple sites. Apply now to help shape the future of pharmaceutical manufacturing!

Your role

This pivotal role combines leadership, technical expertise, innovation, and global collaboration.

Leadership and Innovation
  • Lead development of pre-filled syringe technologies, including formulation, filling, and device assembly.
  • Drive innovation in PFS product design and manufacturing processes for scalability and robustness.
  • Serve as the subject matter expert for pre-filled syringe technologies, promoting knowledge sharing and collaboration.
Project Execution
  • Manage projects from R&D to commercial manufacturing, ensuring milestones are achieved on time and within budget.
  • Oversee tech transfer processes, ensuring seamless scale-up and integration into manufacturing sites.
  • Collaborate with scientists, engineers, and regulatory experts to ensure product success.
Process Optimization and Troubleshooting
  • Design and optimize processes to enhance quality, efficiency, and compliance.
  • Address complex technical challenges to ensure reliable manufacturing outcomes.
Regulatory and Compliance
  • Ensure full compliance with GMP and regulatory standards during development and manufacturing.
  • Assist in preparing technical documentation for regulatory submissions and audits.
Global Collaboration
  • Work with international teams, contributing to and learning from a global network of experts.
  • Travel internationally for on-site project support, training, and troubleshooting.
Your profile

Experience:

  • At least 7+ years of hands-on experience in pre-filled syringe technology, from development to manufacturing.
  • Proven success in bringing pre-filled syringe products to market.
  • Experience in tech transfer and managing large-scale projects.

Education and Background:

  • Degree in Pharmacy, Engineering, or related fields; advanced degrees preferred.

Technical Expertise:

  • Expertise in troubleshooting, process optimization, and scale-up of PFS technologies.
  • Knowledge of regulatory and quality standards specific to pre-filled syringes.

Leadership and Communication:

  • Strong leadership skills to inspire and guide teams.
  • Excellent communication skills for technical and stakeholder engagement.
Working at Siegfried
  • Performance-based incentives.
  • 37.5 hours/week, 30 vacation days, additional leave.
  • Employee discounts, health services, parking, and public transport access.
Who we are

Siegfried is a leading CDMO specializing in active pharmaceutical ingredients, intermediates, and finished dosage forms, with a global presence and a commitment to quality, efficiency, and safety.

Our site in Hameln specializes in sterile medicinal products, including contract manufacturing of parenteral solutions and complex preparations, with a focus on sterile product transfer and establishment.

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