Job Description
Join us in making a real difference to patients worldwide by leading compliant agile logistics operations across our Global Clinical Supply Chain. Youll guide a talented team through the complexities of international trade while fostering innovation ensuring compliance and creating an environment where everyone can thrive and grow. We welcome candidates from all backgrounds who bring different perspectives experiences and approaches to problem-solving. If youre passionate about patient impact energized by complexity and committed to growing others while growing yourself wed love to hear from you.
The Position
As Associate Director Logistics & Regions youll lead compliant import and export operations across EU and rest of world markets ensuring clinical trial materials move efficiently through customs while meeting all regulatory requirements. Youll drive compliance through audits SOPs and strategic projects while building a patient-focused agile supply chain. Success in this role requires strong leadership a collaborative mindset and a solution-oriented approach. Youll work across time zones with diverse stakeholdersincluding Quality Assurance Global Trade Compliance Clinical Operations research teams and external partnersto influence GMP and trade policy adherence while solving time-sensitive logistics challenges. Your ability to build relationships adapt to change and balance multiple priorities will be essential as you lead process innovation ensure compliance and develop your team through coaching and day-to-day management.
Welcome to the Team
Our team comprises approximately 40 members organized by core trade functions to ensure coverage and specialization. Responsibilities are divided across five areas: US imports/exports Rest of World operations FTZ (Foreign Trade Zone) projects trade systems (process and technology enablement) and compliance/audits. This structure aligns expertise with regional and regulatory needs while supporting consistent efficient and compliant global trade execution.
Primary Responsibilities
Ability to lead a high performing team
Oversee compliant and delay-free customs clearance and logistics operations ensure correct documentation and provide solutions and support in daily operations.
Drive improvements in compliance processes within Global Clinical Supply in partnership with stakeholders such as Research Quality Learning and Development Global Clinical Trial Operations Global Trade Compliance and research areas of Drug Product Engineering and Development.
Lead project management for logistics distribution foreign trade zone projects trade systems and trade-related initiatives.
Ensure audit and inspection readiness: lead and support internal and external audits prepare logistics maintain documentation and manage responses and corrective and preventive actions.
Manage permits and licenses administration of standard operating procedures and other documents in electronic document management systems and tracking of compliance commitments and metrics.
Create and deliver training and tools to upskill team members and stakeholders in trade operations.
Uphold good manufacturing practice quality standards global trade regulations and company standards; partner with subject matter experts to monitor performance drive continuous improvement and align to strategic goals.
Your Profile
A bachelors degree in Supply Chain Trade or related field is preferred though we welcome candidates with relevant diplomas and substantial hands-on experience
5 years in regulated industriessuch as pharmaceuticals medical devices food or chemicals with strong knowledge of GxP and Trade Compliance regulations
Demonstrated ability to coach inspire and create inclusive environments where everyone can contribute their best
Expertise in Customs and GMP regulationsfor EU and rest of world markets
Technical proficiencywith SAP compliance systems (deviations CAPAs SOP writing) procurement/negotiation (RFP/RFQ processes) and logistics/supply chain management tools
Proven ability to influence and collaborateacross cultures functions and time zones with stakeholders at all levels
Strong project management capabilitieswith comfort balancing strategic initiatives and day-to-day operations plus excellent communication skills in presenting to diverse audiences
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What we offer
We welcome you to a truly global dynamic and challenging environment with great opportunities for personal development. Our benefits are very competitive and the summary below will give you an idea of what you can expect.
Competitive salary and a 3% year-end bonus;
355 days of leave;
Attractive collective health care insurance package with considerable reduction rates;
Solid Pension Plan;
Incentive Plan;
Numerous training coaching and e-learning modules for long term job opportunities and development.
Required Skills:
Accountability Accountability Adaptability Business Creativity Clinical Supply Chain Management Clinical Trials Confidentiality Cross-Cultural Awareness Customer-Focused Data Analysis GMP Compliance Influencing Without Authority International Logistics Inventory Control Management Leadership Logistics Logistics Management Microsoft Products Process Improvements Procurement Production Planning Project Management Stakeholder Engagement Supply Chain Processes Team Coaching 3 morePreferred Skills:
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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:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
HybridShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
11/27/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Director
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more