Device & Packaging Senior Expert

Proclinical is seeking a Senior Packaging & Delivery Specialist for an exciting on-site role. This role is initially a fixed-term contract, with extension opportunities based on operational demand and funding. In this role, you'll lead the design and development of packaging formats and oral drug delivery technologies, supporting the full product lifecycle-from early-stage formulation through to commercial manufacturing. Strong expertise in pharma packaging, drug delivery, and devices, with excellent collaboration skills.

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:

• Plan and manage projects thoroughly.
• Define product requirements and qualify oral packaging and drug delivery systems, including drug-device combination products and medical devices.
• Collaborate with development and business partners, monitoring progress and providing technical support.
• Oversee the development and implementation of manufacturing processes.
• Provide expertise in primary packaging and devices within cross-functional drug product development teams.
• Evaluate and challenge technical solutions.
• Coordinate the manufacturing of clinical materials and production scale-up.
• Support cross-functional teams in regulatory dossier development, review, and submission.
• Lead risk management activities and monitor Human Factors Engineering efforts.
• Supervise design verification activities and ensure high-quality Design History Files.
• Author and lead the creation of technical documentation.
• Facilitate the transfer of Design History Files to production.

Key Skills and Requirements:

• Degree in Packaging Science, Mechanical Engineering, or a related field.
• Strong experience in pharmaceutical packaging or drug delivery device development.
• Fluency in English; proficiency in German or French is advantageous.
• Solid understanding of pharmaceutical development processes.
• Familiarity with medical device regulations (FDA 21CFR 820, EU Medical Device Directive/Regulation).
• Experience in technical documentation, including Design Control processes and regulatory aspects.
• Knowledge of mechanical/industrial engineering, product design, and test/verification methods.
• Understanding of Human Factors Engineering, risk management, and clinical study requirements.
• Excellent communication and conflict resolution skills.

If you are having difficulty in applying or if you have any questions, please contact Emile de Beer at e.debeer@proclinical.com.

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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