Director

• Lead the strategic governance and continuous improvement of the global pharmacovigilance system framework
• Oversee the governance of pharmacovigilance regulatory intelligence, process management, organizational training, and change implementation
• Chair or facilitate regulatory intelligence governance board
• Provide strategic recommendations to the EU QPPV and senior leadership regarding implementation priorities and compliance risks
• Drive the design, implementation, review, and optimisation of pharmacovigilance processes, standards, procedures, and ways of working
• Develop and oversee the global pharmacovigilance training governance framework
• Lead and develop a team of Process Excellence professionals

Director of Pharmacovigilance Process Excellence

• Own the global dairy enzymes portfolio, including SKU optimization, lifecycle management, and strategic positioning.
• Develop and manage the innovation pipeline in collaboration with R&D, Applications, and Commercial teams.
• Drive profitability and growth through pricing strategies, cost management, and value creation.
• Lead cross-functional teams to execute successful product launches, including go-to-market planning, training, and post-launch evaluation.
• Support key customer interactions, co-development initiatives, and technical troubleshooting.
• Contribute to long-term strategy for dairy enzymes, identifying market trends, competitive insights, and growth opportunities.
• Work closely with Regulatory, Supply Chain, Sales, and Marketing to ensure alignment and execution.

Global Associate Director – Dairy Enzymes

• Lead rare disease HTA statistical strategy from planning through delivery.
• Drive strategic statistical input to evidence generation plans, HTA submissions and payer evidence packages across the portfolio.
• Synthesise evidence across clinical trials, indirect treatment comparisons and real-world evidence.
• Translate statistical requirements of AMNOG, NICE, HAS and EU HTA joint clinical assessments.
• Build methodological frameworks where standard approaches break down.
• Develop and validate statistical approaches for comparative effectiveness.
• Determine what's scientifically defensible and what HTA bodies will accept.
• Drive strategic oversight to ensure methodological coherence across the portfolio.
• Influence without authority and build capability.
• Represent the organisation at scientific advice meetings and HTA body interactions.
• Mentor team members, lead methodological working groups, contribute to publications, and drive knowledge sharing on rare disease HTA approaches.

Associate Statistical Director – Cross-Trial Evidence, HTA

• Lead an organization of 40 employees in Liquid & Sterile Production
• Optimize and develop the production area to meet future product demands
• Ensure robust GMP/GxP compliance across all activities
• Lead continuous improvements and productivity initiatives
• Collaborate closely with Quality Assurance, Supply Chain, Engineering, and global stakeholders
• Responsible for budget planning and execution of operational expenses

Senior Director, Liquid & Sterile Production

• Set strategic direction and lead the execution of comprehensive Total Rewards solutions
• Combine strategic insight, data-driven decision-making and strong stakeholder collaboration
• Lead a global team of 11 Total Rewards professionals supporting Europe (excluding HQ), Canada and Emerging Markets
• Use internal and external market data to design competitive, compliant and scalable reward solutions aligned with business strategy
• Partner with senior leaders, HRBPs and Total Rewards HQ teams
• Develop team capability through knowledge sharing, coaching and a strong focus on continuous improvement

Director jobs in Denmark

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Director of Pharmacovigilance Process Excellence

Global Associate Director – Dairy Enzymes

Associate Statistical Director – Cross-Trial Evidence, HTA

Senior Director, Liquid & Sterile Production

Director, Global Total Rewards