Senior Manager - Drug-Device Packaging & Strategy

LEO Pharma; Ballerup; On-site; DKK 180,000 - 240,000; Full time

Job summary

LEO Pharma seeks a Senior Manager for Device & Packaging to lead strategy, development, qualification, and lifecycle management of drug-device combination products and packaging solutions. You will provide technical leadership across development, commercialization, tech transfer, launches, and post-approval changes.

Based in Ballerup, Denmark, you will manage a team of SMEs, drive continuous improvement, and collaborate with Quality, Regulatory Affairs, and external partners to ensure GMP

Qualifications

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

Responsibilities

• Lead strategy, development, qualification, and lifecycle management of drug-device combo products and packaging.
• Provide technical leadership across development, commercialization, tech transfer, launches, and post-approval changes.
• Manage resource planning, project priorities, timelines, and team deliverables.
• Collaborate with Quality, Regulatory Affairs, external partners, and governance forums.

Skills

Team leadership

Technical leadership

Regulatory expertise

GMP knowledge

Design controls

Risk management

Change control

CAPA management

Project management

Education

Engineering degree

Pharmaceutical Sciences degree

Materials Science degree

Life Sciences degree

Tools

Quality Management System (QMS)

Regulatory databases

Job description

LEO Pharma seeks a Senior Manager for Device & Packaging to lead strategy, development, qualification, and lifecycle management of drug-device combination products and packaging solutions. You will provide technical leadership across development, commercialization, tech transfer, launches, and post-approval changes.

Based in Ballerup, Denmark, you will manage a team of SMEs, drive continuous improvement, and collaborate with Quality, Regulatory Affairs, and external partners to ensure GMP