Senior Manager, Drug-Device Packaging & Lifecycle

LEO Pharma; København; On-site; DKK 1,200,000 - 1,600,000; Full time

Job summary

LEO Pharma is seeking a Senior Manager for Device & Packaging to lead a team of subject matter experts in Ballerup, Denmark. You will shape strategy for drug-device combinations, guide development, qualification, launches, and post‑approval changes, while ensuring GMP, regulatory, and design control compliance across lifecycle activities.

You will partner with Quality, Regulatory Affairs, and external manufacturing to drive continuous improvement and successful product commercialization in a

Qualifications

• A degree in Engineering, Pharmaceutical Sciences, Materials Science, Life Sciences, or another relevant discipline.
• Relevant experience in pharma/biotech/medical devices or combination products.
• Experience with drug-device combination products, primary/secondary packaging.
• Prior people management or team leadership experience.
• Good knowledge of GMP, design controls, risk management, change control, and regulatory expectations.

Responsibilities

• Lead strategy, development, qualification, and lifecycle management of drug-device combination products and packaging.
• Provide technical leadership across development, commercialization, tech transfer, launches, and post-approval changes.
• Ensure compliance with global regulatory, quality, GMP, and design control requirements.
• Manage resource planning, project priorities, timelines, and team deliverables.
• Represent the function in governance forums, project teams, and external partner discussions.

Skills

Leadership

Regulatory expertise

GMP knowledge

Design controls

Risk management

Education

Engineering or Life Sciences degree

Job description

LEO Pharma is seeking a Senior Manager for Device & Packaging to lead a team of subject matter experts in Ballerup, Denmark. You will shape strategy for drug-device combinations, guide development, qualification, launches, and post‑approval changes, while ensuring GMP, regulatory, and design control compliance across lifecycle activities.

You will partner with Quality, Regulatory Affairs, and external manufacturing to drive continuous improvement and successful product commercialization in a