Join a multi-disciplinary team supporting the cGMP production of clinical-scale Active Pharmaceutical Ingredients (APIs). In this hands-on manufacturing role, you'll support API development through equipment operation, batch execution, documentation, and continuous improvement activities.Typical process operations include:Charging solids and liquids to vesselsDistillation, extraction, and phase separationCrystallization, filtration, and dryingEquipment cleaning and preparationKey ResponsibilitiesExecute process instructions and batch records in a cGMP environment.Prepare, operate, monitor, sample, and clean pharmaceutical manufacturing equipment.Support equipment commissioning, qualification, and troubleshooting activities.Complete manufacturing documentation, including batch records, cleaning records, and in-process sampling documentation.Follow cGMP, safety, environmental, and site procedures at all times.Report deviations, safety concerns, and quality observations promptly.Manage manufacturing waste according to approved procedures.Participate in shift handovers and maintain clear communication across teams.Collaborate with Quality, Compliance, Process Chemistry, Tech Transfer, and Production teams.Support SOP reviews and continuous improvement initiatives.Manage priorities independently and assist less-experienced team members as needed.Complete required training and participate in site safety programs.Perform routine material handling activities, including lifting and moving items up to 50 lbs.
