Description

In this role, you will provide expert guidance on quality and regulatory compliance in healthcare, lead impactful projects, and ensure continuous improvement while collaborating with both internal and external stakeholders.

Requirements

• •Bachelor’s degree or equivalent in healthcare quality, safety, transportation, business, information systems, computer science, or related discipline
• •Minimum five years of experience in pharma quality in manufacturing, laboratories, distribution, or closely related experience
• •Deviation experience in pharma and healthcare
• •Excellent level in English
• •Business travel required
• •Proficient Office 365 skills
• •Strong management, human relations, project management, analytical, and communication skills
• •Ability to present clearly, both orally and in writing
• •Collaboration with business areas, customers, vendors, systems users, and technical developers
• •Knowledge in European regulatory compliance in pharma and healthcare
• •Lean/Six Sigma training preferred

Tasks

• •Provide technical expertise to senior management
• •Deliver analysis and interpretation of complex information
• •Lead high-impact cross-functional projects
• •Drive strategic planning initiatives
• •Support cross-functional project teams for optimal results
• •Plan and direct quality management processes in pharma or healthcare
• •Offer quality guidance to external customers and regulatory bodies
• •Advise internal stakeholders on quality matters
• •Utilize electronic quality systems in compliance with regulations
• •Identify and manage continuous improvement projects
• •Conduct deviation investigations and CAPAs
• •Review Quality Agreements and Supplier Qualifications
• •Perform training for GDP, IATA, and CEIV certifications
• •Complete other assigned duties

Tools & Technologies

Benefits