Job Description

Key Responsibilities

The Production Supervisors will oversee day-to-day manufacturing activities and ensure that production targets are achieved in accordance with approved procedures, GMP requirements, quality standards, and safety requirements.

Key responsibilities will include:

• Supervising daily production activities and production personnel.
• Ensuring production schedules and targets are achieved.
• Ensuring manufacturing processes are performed according to approved SOPs and batch manufacturing records.
• Supervising sterile IV pharmaceutical manufacturing activities.
• Ensuring compliance with Good Manufacturing Practices (GMP).
• Monitoring production processes and identifying deviations.
• Working closely with QA and QC to resolve quality and production issues.
• Ensuring proper documentation of production activities.
• Monitoring production equipment and reporting breakdowns promptly.
• Coordinating with Engineering for equipment maintenance.
• Managing production personnel and allocating duties effectively.
• Monitoring production performance and productivity.
• Ensuring proper housekeeping and workplace safety.
• Participating in investigations of deviations, non-conformances, and corrective actions.
• Supporting continuous improvement initiatives.

Qualifications and Experience

• Bachelor’s Degree or Diploma in Pharmaceutical Manufacturing, Pharmaceutical Sciences, Chemical Engineering, Industrial Production, or a related field.
• Minimum 5 years of relevant experience in a manufacturing industry.
• Demonstrated experience supervising production teams.
• Experience in pharmaceutical manufacturing will be a significant advantage.
• Knowledge of GMP, production documentation, quality systems, and occupational safety.
• Strong leadership and people-management skills.
• Ability to work under pressure and meet production targets.

• Supervising daily production activities and production personnel.
• Ensuring production schedules and targets are achieved.
• Ensuring manufacturing processes are performed according to approved SOPs and batch manufacturing records.
• Supervising sterile IV pharmaceutical manufacturing activities.
• Ensuring compliance with Good Manufacturing Practices (GMP).
• Monitoring production processes and identifying deviations.
• Working closely with QA and QC to resolve quality and production issues.
• Ensuring proper documentation of production activities.
• Monitoring production equipment and reporting breakdowns promptly.
• Coordinating with Engineering for equipment maintenance.
• Managing production personnel and allocating duties effectively.
• Monitoring production performance and productivity.
• Ensuring proper housekeeping and workplace safety.
• Participating in investigations of deviations, non-conformances, and corrective actions.
• Supporting continuous improvement initiatives.

• Strong leadership and people-management skills.
• Ability to work under pressure and meet production targets.
• Knowledge of GMP, production documentation, quality systems, and occupational safety.

• Bachelor’s Degree or Diploma in Pharmaceutical Manufacturing, Pharmaceutical Sciences, Chemical Engineering, Industrial Production, or a related field.
• Demonstrated experience supervising production teams.
• Experience in pharmaceutical manufacturing will be a significant advantage.