We are seeking an experienced Project Manager with strong expertise in parenteral manufacturing and pharmaceutical engineering.Key Responsibilities:Lead qualification and validation of parenteral equipment (e.g. fill-finish lines, autoclaves, lyophilizers, CIP/SIP systems).Manage aseptic process simulations (media fills, re-validations).Define scope, planning, budgets, and lead project teams.Oversee equipment specifications, FAT/SAT, commissioning, and construction works.Ensure compliance with GMP and regulatory standards, including risk assessments and deviation management.Support troubleshooting and continuous improvement initiatives.Requirements:Master's degree in Engineering or related field (or equivalent experience).5+ years' experience in pharmaceutical engineering and GMP qualification.Strong knowledge of aseptic processes and parenteral manufacturing equipment.
