Associate Specialist, Global Submissions Publishing in Hyderabad, भारत
Merck
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
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