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 compliance,identifyrisk, 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 inbiologics,sterile, orothercomplex 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%
Required Skills:
Adaptability, Cross-Team Collaboration, Global Team Collaboration, GMP Auditing, Influencing Skills, Inspection Readiness, Pharmaceutical Industry, Pharmaceutical Supply Chain, Problem Solving, Quality Risk Management, Regulatory Compliance, Stakeholder Management, Technical Writing
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Secondary Language(s) Job Description:
We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's 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.
Pleasedon'thesitate 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 needs, please apply today.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Remote
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
08/28/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
