Drug Delivery Systems Engineer

Proclinical; Bern; Vor Ort; CHF 110.000 - 140.000; Vollzeit

Zusammenfassung

Proclinical is seeking a Drug Delivery Systems Engineer to contribute to the development and optimization of combination products, including drug delivery devices for respiratory, subcutaneous, and intravenous applications. This role involves technical design, risk management, and collaboration with cross-functional teams to ensure project execution and compliance with industry standards.

Please note that to be considered for this role you must have the right to work in this location or hold an

Qualifikationen

• Advanced degree in a relevant engineering field.
• Strong background in combination products and drug delivery systems.
• Experience with regulatory and quality documentation.

Aufgaben

• Execute portfolio projects within timelines, quality, and cost targets.
• Develop design controls and risk management documentation.
• Improve design, development, specification, integration, and tech transfer processes.
• Collaborate with R&D, Technical Operations, Quality, and Operations teams.
• Stay updated on legislation, regulations, and industry trends.
• Provide data-driven insights and support for queries.

Kenntnisse

Independent work

Team collaboration

Communication skills

English proficiency

Ausbildung

Master's or PhD in Biomedical/Electrical/Mechanical Engineering

Jobbeschreibung

Ready to shape the next generation of drug delivery devices and bring life-changing therapies closer to patients?

Proclinical is seeking a Drug Delivery Systems Engineer to contribute to the development and optimization of combination products, including drug delivery devices for respiratory, subcutaneous, and intravenous applications. This role involves technical design, risk management, and collaboration with cross-functional teams to ensure seamless project execution and compliance with industry standards.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Execute portfolio projects within agreed timelines, quality, and cost parameters to deliver competitive combination products and production processes.
• Develop technical design controls and risk management documentation.
• Contribute to the improvement of design, development, customization, specification, integration, qualification, and technology transfer processes for combination products.
• Collaborate with R&D, Technical Operations, Quality, and Operations teams to align strategies and ensure smooth project handovers.
• Stay updated on relevant legislation, regulations, guidance, and industry trends in the field of combination products.
• Provide data-driven insights, professional judgment, and support for business, technical, and project-related queries.

Key Skills and Requirements:

• Advanced degree (Master's or PhD) in Biomedical, Electrical, Mechanical Engineering, or a related field.
• Strong scientific background in combination products and drug delivery systems.
• Experience in regulatory and quality standards, including documentation for quality assessments and regulatory submissions.
• Proven ability to work independently and collaboratively with diverse teams, demonstrating strong organizational and communication skills.
• Familiarity with design control and risk management processes.
• Proficiency in English.