Research Associate III

Job Description:

 Responsibilities

• Provide technical leadership and subject?matter expertise across product lifecycle management activities.
• Independently own and execute product design changes and new product registrations, ensuring compliance with international, regional, and national regulatory requirements.
• Lead technical assessments and define strategies for changes related to formulation, design, labeling, raw materials, manufacturing support, quality improvement, and regulatory compliance.
• Develop technically sound, data?driven solutions in collaboration with senior scientists and global partners.
• Project & Stakeholder Management
• Lead and coordinate cross?functional technical activities with global stakeholders to meet project commitments, quality standards, and business objectives.
• Proactively follow up and drive alignment across functions such as R&D, Regulatory Affairs, Quality, Operations, and Supply Chain.
• Provide clear, concise, and timely technical updates to senior management and key stakeholders.

Qualification & Experience

• Master’s degree in Chemistry, Pharmacy, or a related scientific discipline.
• Minimum 10 years of relevant experience in pharmaceutical or medical products R&D, lifecycle management, or regulated product development.