Associate Director – Global Auditing

Join a global qualityorganisationand play a key role in safeguarding product quality compliance and patient supply across an international manufacturing and supply network.

As an Associate Director Auditor you will conduct audits across manufacturing sites suppliers contractors and distribution partners throughout Europe and beyond. This role offers unique exposure to a broad range of technologies products and manufacturing environments including biologics sterile products vaccines APIs and emerging therapies.

Working as part of a highly experienced global audit team you will help assess complianceidentifyrisk and drive continuous improvement across a complex global supply chain. The successful candidate can be based anywhere in Europe and should be comfortable with regular international travel.

Bring energy knowledge and innovation to carry out the following:

• Conduct GMP and GDP audits across manufacturing sites suppliers contractors business partners and distribution networks.

• Assess compliance with regulatory requirements quality systems and industry standards.

• Support due diligence activities supplier qualification and pre-approvalinspectionreadiness assessments.

• Prepare for conduct and document audits ensuring clear andtimelyreporting of observations and recommendations.

• Partner with stakeholders across manufacturing quality supply chain and compliance functions to support risk mitigation and continuous improvement.

• Maintain knowledge of evolving regulatory requirements industry trends and best practices.

• Support projects and initiatives that enhance auditprogrammeeffectiveness and efficiency.

• Influence quality and compliance standards across a diverse global manufacturing network.

• Build strong relationships with internal and external stakeholders whileoperatingindependently across multiple locations and cultures.

What Skills You Will Need

• Degree in Science Engineering Chemistry Biology ora relateddiscipline.

• Significant experiencewithin the pharmaceuticalindustryor as a regulator.

• Strong knowledge of GMP requirements and quality systems supporting pharmaceutical manufacturing.

• Experience in Quality Manufacturing Compliance Auditing or related regulated functions.

• Previousauditing experience within GMP-regulated environments.

• Experience inbiologicssterileorothercomplex pharmaceutical operations isadvantageous.

• Strong understanding of quality risk management regulatory expectations and compliance principles.

• Excellent communication influencing negotiation andreport-writingskills.

• Ability to work independently while collaborating effectively across global teams.

• Willingness to travel regularly across Europe and other international locations.

• Comfortable with travel up to 50%

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the worlds most challenging healthcare needs.

As an equal opportunity employer we are proud to be a company that embraces the value of bringinginclusive talented and committed people together.

Pleasedonthesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application.

So if you are ready to:

Invent solutions to meet unmet healthcare needsplease apply today.