Job Description Supervise the development, scale-up and transfer, and validation of formulations and manufacturing processes for new OTC products (Global Business Unit). Acts as the Core team member on assigned projects. Lead a small technical team. • Manage all project-related development activities. • Manage the development process for the new product formulations through launch, including budgeting and creating timelines • Select appropriate formulations for progressing through development. • Supervise the research, development and validation of formulations and manufacturing processes for new OTC products. • Participate as a core team member in Project Teams, assessing the viability of proposed projects, trouble-shooting, finding solutions and championing new product ideas in a Global Business Environment. • Perform technical due diligence and review technical documentation for new project op-portunities. • Lead Scientists and Senior Scientists in order to manage projects against timelines and budgets while maintaining high quality standards. • Supervise manufacturing of GMP batches. • Participate in the purchasing of new GMP equipment. • Apply GMP rules including to the pilot lab facility. • Write CMC sections of registration files. • Serve as subject matter expert for all R&D associates in relevant disciplines . Interested candidates can apply for the same before 25th April'14 .
Phama Job Categories:
Research and Development