Job Description
- 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.
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