Description

In this role, you will focus on developing innovative syringe systems for radioligand therapies. You will collaborate with diverse teams to tackle design challenges and ensure compliance, while also contributing to the documentation and registration of medical devices.

Requirements

• •Master’s or PhD in engineering, materials science, pharmaceutical technology, or related discipline
• •Minimum of 3 years’ experience in a comparable position, ideally within primary packaging, medical device, combination product development, or pharmaceutical industries
• •Experience with radioligand therapies (RLT) is a significant plus
• •Strong communication and negotiation abilities
• •Ability to lead and influence within a global, matrixed organization
• •Effective collaboration across different functional areas
• •Excellent verbal and written communication skills in English

Tasks

• •Lead the development of syringe systems for radioligand therapies
• •Collaborate with interdisciplinary project teams
• •Manage design history documentation for assigned projects
• •Utilize technical expertise to resolve design and operational challenges
• •Ensure timely preparation and delivery of parenteral primary packaging
• •Perform technical assessments to confirm compliance of packaging components
• •Apply knowledge of materials and manufacturing methods
• •Address and resolve problems within your area of responsibility
• •Communicate solutions effectively across organizational boundaries
• •Develop packaging prototypes using rapid prototyping techniques
• •Conduct assessments for manufacturability and perform tolerance stack analyses
• •Stay current in materials, design, and manufacturing fields
• •Contribute to platform documentation and technology landscaping
• •Drive preparation of technical documentation for medical device registration
• •Support responses to health authority inquiries

Benefits