Regional Dossier Publisher

Job Description

We are looking for a highly skilled Regional Dossier Publisher (RDP) to support regulatory submission publishing activities across the EU +EEMEA region. In this role, you will be responsible for the assembly, publishing, and delivery of regulatory dossiers, while supporting country Regulatory Affairs teams and contributing to process improvements, system readiness, and standardization efforts.

The ideal candidate will bring strong publishing expertise, technical knowledge of regional regulatory requirements, and hands-on experience with electronic submission tools and document management systems.

Key Responsibilities

As a Regional Dossier Publisher, you will:

• Serve as the regional subject matter expert for regulatory submission publishing, including dossier structures, file formats, electronic submissions, transmission gateways, and dossier repositories.

• Identify, maintain, and apply dossier format requirements to support the assembly and delivery of regulatory submissions to health authorities and country organizations.

• Support country Regulatory Affairs teams with local publishing and submission transmission needs to help ensure critical deadlines are met.

• Collaborate with central publishing teams to maintain and execute publishing processes in line with regional and country requirements.

• Promote standardization across supported countries and encourage consistent publishing practices.

• Lead technical impact assessments for regional and country regulatory submission requirements.

• Provide technical guidance and training to country Regulatory Affairs teams on publishing processes and tools.

• Act as a technical point of contact for health and regulatory authorities in the region.

• Support the maintenance and validation of processes and systems related to regulatory submission assembly and delivery.

• Perform publishing activities to meet key submission timelines.

• Participate in improvement projects, including system testing, readiness activities, and performance measurement initiatives.

• Support technical validation efforts.

• Mentor, coach, and manage external publishing resources as needed.

Required Experience and Skills

Experience:

• Minimum 4 years of publishing experience in regulatory submissions.

• Hands-on experience with Ennov Insight Publisher and/or Lorenz Docubridge.

• Experience supporting EU and EEMEA publishing requirements is required.

• Knowledge of regulatory registration procedures in the EU and EEMEA is considered a plus.

Technical Skills:

• MS Office applications
• Adobe Acrobat
• MS Project
• Document Management Systems
• Proven ability to work with a variety of technical applications and publishing systems.
• Familiarity with dossier assembly, electronic submission formats, and submission transmission tools.

Core Competencies:

• Strong analytical skills and attention to detail.

• Excellent customer service and communication skills.

• Ability to work effectively with stakeholders at different levels and across departments.

• Proven ability to work under pressure and meet tight deadlines.

• Strong organizational skills and a proactive, solution-oriented mindset.

What We Offer:

• A dynamic role within a highly collaborative regulatory operations environment.

• The opportunity to work on important regional submission activities across EU +EEMEA.

• Exposure to a broad range of regulatory publishing processes, systems, and improvement initiatives.

• The chance to contribute to standardization, technical readiness, and continuous improvement efforts.

• Opportunities to support, train, and mentor colleagues and external resources.

• A role with meaningful impact on the timely delivery of critical regulatory submissions.

Required Skills:

Adaptability, Adaptability, Adobe Acrobat, Assembly Processes, Audits Compliance, Customer Service, Detail-Oriented, Document Management, Drug Regulatory Affairs, Electronic Document Management System (EDMS), Employee Training Programs, Global Communications, Improvement Projects, International Standardization, Maintenance Management, Pharmaceutical Regulatory Affairs, Pharmacovigilance, Process Improvements, Process Management, Project Management, Publishing Process, Regulatory Affairs Management, Regulatory Awareness, Regulatory Compliance, Regulatory Operations {+ 2 more}

Preferred Skills:

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Current Contingent Workers apply HERE

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

07/6/2026

***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. **