Estimate costs and prepare budgets.Organize workflow to meet specifications and deadlines.Monitor production to resolve issues.Supervise and evaluate the performance of production personnel (quality inspectors, workers, etc.).Approve maintenance work, purchasing of equipment, etc.Check that the manufacturing process meets all quality standards and health and safety regulations.Ensure that good GMP standards are maintained at all times.Monitor productivity and improve this where necessary.Organize the repair or replacement of damaged or faulty equipment.Collect data and produce reports.Liaise with other departments and supervise the team members.Identify risks and opportunities.Prepare the production site for MOH audits.Responsible for assuring compliance with all regulatory requirements.Perform the analytical review, recommend, and implement corrective action for any exception condition.Improve OEE and decrease stoppage.

Requirements:

Familiarity with the production of solid products, tablets, capsules, liquids, and highly potent drugs.Effective experience in related positions.Familiarity with the pharmaceutical production process.Ability to provide appropriate solutions to improve and resolve problems.Familiarity with GMP standards.Familiarity with project management.