Regulatory Associate Manager - Product Variations, CD CMC

GSK is seeking a Regulatory Associate Manager - Product Variations to lead regulatory work for product variations within Clinical Development CMC. The role will provide opportunities to collaborate with global teams and contribute to meaningful work for patients.

Requirements

• Bachelor’s degree in chemistry, pharmacy, pharmaceutical sciences or a related science/technical field
• Minimum 5 years of regulatory affairs experience with a focus on CMC and product variations
• Experience preparing or managing CMC dossiers for regulatory submissions
• Knowledge of global regulatory guidelines and expectations for CMC content
• Strong organisational skills and experience managing multiple projects and deadlines
• Good written and verbal communication skills in English for clear, concise dossier writing and stakeholder engagement

Benefits

• Global career opportunities
• Supportive, high-impact team that values learning and career development
• Opportunities to contribute to meaningful work for patients