Regulatory Affairs Consultant - Head

As a Regulatory Affairs Consultant - Head, you will leverage your minimum of 10 years of Life Science industry experience to provide substantial expertise in regulatory affairs. Your hands-on experience in Chemistry, Manufacturing, and labeling processing will be crucial in ensuring compliance with global regulatory standards such as FDA, EMA, ICH, and other international regulations. Your excellent communication skills, both written and verbal, will be essential in effectively conveying regulatory requirements within the organization. Key Responsibilities: - Demonstrating expertise in CMC and labeling processes - Ensuring compliance with global regulatory frameworks including FDA, EMA, and ICH - Applying Good Clinical Practice standards - Implementing Quality Management Systems in outsourcing scenarios Qualifications Required: - Bachelor's degree in a relevant field - Proficiency in project management and cross-functional collaboration - Strong analytical and problem-solving skills - Ability to navigate and interpret complex regulatory landscapes across multiple regions Additionally, your meticulous attention to detail, organizational prowess, and ability to work with cross-functional teams will be essential in ensuring successful regulatory compliance. Your in-depth understanding of Quality Management Systems in outsourcing scenarios will further strengthen the organization's regulatory processes. Please note that the job code for this position is GO/JC/1061/2025, and the recruiter for this role is Maheshwari Balasubramanian.,