Assistant Manager - Project Management

As a Project Manager in the Formulation R&D department, your role involves managing end-to-end formulation projects, coordinating with various functions, ensuring regulatory compliance, managing materials and vendors, and driving continuous improvement initiatives. **Key Responsibilities:** - Manage end-to-end formulation R&D projects, from concept to exhibit/validation batch and technology transfer. - Develop and track detailed project plans, timelines, and milestones. - Coordinate with various departments such as Formulation R&D, Analytical R&D, Regulatory Affairs, Quality Assurance, Production, Purchase, and Supply Chain. - Ensure compliance with cGMP, data integrity, and internal quality systems. - Identify and mitigate technical, regulatory, and supply risks related to formulation development. - Coordinate with Purchase for material procurement, vendor qualification, and cost management activities. **Qualifications Required:** - Masters degree in Pharmacy, Life Sciences, Chemistry, or related field. - 7-12 years of project management or relevant experience in regulated/emerging markets in the pharma industry. - Strong knowledge of regulatory pathways, GMP/GxP, and submission processes. - Proven ability to manage multiple projects simultaneously. - Excellent communication, leadership, and stakeholder-management skills. - Proficiency in project management tools (MS Project, Word, Excel, etc.) is desirable. This role requires a detail-oriented individual with strong analytical and problem-solving skills, the ability to work in cross-functional environments, and effective communication skills. You will report to the Head of Project Management. As a Project Manager in the Formulation R&D department, your role involves managing end-to-end formulation projects, coordinating with various functions, ensuring regulatory compliance, managing materials and vendors, and driving continuous improvement initiatives. **Key Responsibilities:** - Manage end-to-end formulation R&D projects, from concept to exhibit/validation batch and technology transfer. - Develop and track detailed project plans, timelines, and milestones. - Coordinate with various departments such as Formulation R&D, Analytical R&D, Regulatory Affairs, Quality Assurance, Production, Purchase, and Supply Chain. - Ensure compliance with cGMP, data integrity, and internal quality systems. - Identify and mitigate technical, regulatory, and supply risks related to formulation development. - Coordinate with Purchase for material procurement, vendor qualification, and cost management activities. **Qualifications Required:** - Masters degree in Pharmacy, Life Sciences, Chemistry, or related field. - 7-12 years of project management or relevant experience in regulated/emerging markets in the pharma industry. - Strong knowledge of regulatory pathways, GMP/GxP, and submission processes. - Proven ability to manage multiple projects simultaneously. - Excellent communication, leadership, and stakeholder-management skills. - Proficiency in project management tools (MS Project, Word, Excel, etc.) is desirable. This role requires a detail-oriented individual with strong analytical and problem-solving skills, the ability to work in cross-functional environments, and effective communication skills. You will report to the Head of Project Management.