Associate Specialist, Global Submissions Publishing in Hyderabad, भारत

Associate Specialist supporting global regulatory submissions publishing at Merck, responsible for assembling, verifying, and delivering high-quality regulatory dossiers to health authorities. Role involves quality control, process testing, and cross-functional collaboration to meet regulatory timelines and compliance standards.

Responsibilities

• Execute publishing workflows including quality control, verification, and finalization of submission dossiers
• Ensure regulatory submissions meet specified deadlines and comply with health authority requirements
• Collaborate with authors and stakeholders to achieve high-quality deliverables
• Test and provide feedback on new publishing tools and process improvements
• Develop and maintain administrative documentation including procedures and training materials

Requirements

• High school diploma or equivalent
• Proficiency with MS Word and Adobe Acrobat Professional
• Strong organizational and time management skills for multiple concurrent assignments
• Excellent written and verbal communication in English and regional languages
• Understanding of regulatory compliance principles and quality assurance practices
• Problem-solving ability and adaptability to changing processes
• Collaborative interpersonal skills and cultural awareness