Join the NuVvaGen Bioscience P. Ltd. team as a Full Time Manager – Regulatory on Erekrut, specializing in Manager – Regulatory in the Manufacturing industry. We are seeking talented individuals with a passion for Pharmaceutical and educational qualifications ranging from 4-6 Years. Apply now on Erekrut to take the next step in your career with a leading global company.
Job Description
Department: Regulatory Affairs
Designation: Manager – Regulatory
Job Location: Palghar (Near to Mumbai)
Experience: 5+ years of experience in Regulatory
Job Summary: Procuring raw materials, packaging materials, and other supplies needed for production and operations. This includes sourcing suppliers, negotiating contracts, managing inventory and ensuring compliance with regulatory standards like GMP.
Responsibilities:
Regulatory Strategy and Submissions: Develop and implement regulatory strategies for new and existing products. This includes preparing, submitting, and managing product registration dossiers, notifications,
and applications to various regulatory bodies. The manager must stay informed on the latest regulations to advise on product formulations, claims, and labelling to ensure market entry and continued compliance.
Documentation and Compliance: A core duty is maintaining meticulous records. The manager oversees the creation and maintenance of technical files, safety dossiers, and other documentation required for product registrations. They are responsible for ensuring ongoing compliance with Valuable Manufacturing Practices (GMP), labelling requirements, and advertising standards.
Cross-Functional Collaboration: The regulatory manager works closely with various departments, including Research & Development (R&D;), Quality Assurance, Marketing, and Legal. They provide regulatory guidance throughout the product lifecycle, from initial concept and formulation to marketing and post-market surveillance. For example, they advise the