Regulatory Affairs Associate - Artwork

Roles & Responsibilities
• Prepare, review, and coordinate regulatory documentation and artwork components
• Ensure artwork and labeling compliance with EU, US, and ROW regulatory requirements
• Support regulatory submissions in line with applicable guidelines and standards
• Collaborate with cross-functional teams to meet project timelines and deliverables
• Maintain accurate regulatory records, version control, and documentation archives
• Provide regulatory support for pharmaceutical and healthcare products

Qualification
• Bachelor’s degree in Pharmacy / Life Sciences or related discipline

Experience
• Experience in regulatory documentation and submissions preferred

Skills
• Knowledge of global regulatory compliance requirements (EU / US / ROW)
• Strong analytical and organizational skills
• Excellent written and verbal communication skills in English
• High attention to detail and ability to manage multiple projects
• Ability to work effectively in a team-oriented environment

About the Organization
Neocubes Pharma LLP (Neoplus Translation & Neocubes Pharma) – A regulatory-focused organization delivering high-quality regulatory affairs, pharmacovigilance, and safety monitoring services for EU, US, and ROW markets, offering strong learning and growth opportunities in regulatory documentation and artwork compliance.