Overview
Production Supervisor Jobs in Dammam, Eastern, Saudi Arabia at Tabuk Pharmaceuticals Manufacturing Company
Title: Production Supervisor
Company: Tabuk Pharmaceuticals Manufacturing Company
Location: Dammam, Eastern, Saudi Arabia
We are seeking a Production Supervisor to join our Production team in Dammam. The ideal candidate will manage sterile manufacturing operations, ensuring full adherence to cGMP, safety, and quality requirements. This role demands solid expertise in aseptic processing and practical experience with biosimilar and oncology filling lines. The candidate will lead production teams, uphold operational efficiency, and champion continuous improvement across all sterile production processes.
Main Responsibilities:
- Coordinate and control operations in the assigned production department.
- Supervise adherence to safety, quality, and supply principles.
- Plan and control production resources to meet quality and output targets.
- Ensure cost-effective resource use and full cGMP compliance.
- Maintain high health and safety standards in all production areas.
- Prepare and review production documentation (SOPs, POIs, validation protocols, etc.).
- Attend production planning, GMP, validation, and factory staff meetings.
- Organize training and development per the approved schedule.
- Support planning and future development activities with the Production Manager.
- Participate in internal/external GMP compliance audits.
- Assist R&D in scaling up products and launching new ones.
- Troubleshoot operational issues daily on the shop floor.
- Manage procurement requests for disposables, change parts, and machinery.
- Review production schedules and records to assess output and production needs.
- Coordinate operations across departments with other supervisors.
- Manage and supervise media fill activities.
- Follow up on departmental consumables and preventive maintenance activities.
- Train operators and officers on procedures and protocols.
- Maintain operational data, including time, cost, and production records.
- Maintain cleanliness of the production area.
- Support tasks related to SAP operations.
- Review and update SOPs as scheduled.
- Handle eQMS activities: deviations, CAPA, change controls, risk management, etc.
- Liaise with Engineering for preventative maintenance and equipment troubleshooting.
Qualifications:
- Minimum 10 years in pharmaceutical manufacturing.
- Bachelor’s degree in Pharmacy, Engineering, or a relevant technical field.
- Sterile Background , Aseptic filling , Ampoule , Vial & Lyophilization.
- Additional Experience (Preferred) : ophthalmology , Pre-filled syringe , Isolators.
- Strong leadership and coordination abilities.
- Excellent command of GMP and production documentation.
- Proficiency in SAP and QMS systems.
- Collaborative and solutions-focused mindset.