Production Supervisor (Solid Line) at Deloxe HR

Deloxe is a forward-thinking human resources consulting firm dedicated to optimizing workforce potential and driving organizational success. We deliver innovative HR solutions that empower businesses, enhance employee experiences, and foster sustainable growth. At Deloxe, we are committed to transforming workplaces through strategic HR management and cutting-edge solutions that maximize efficiency and impact.

We are recruiting to fill the position below:

Job Title: Production Supervisor (Solid Line)

Location: Calabar, Cross River 
Employment Type: Full-time

Description

• We are seeking a competent and detail-oriented Production Supervisor (Solid Line) to oversee daily solid dosage pharmaceutical production activities.
• The role involves supervising production processes, ensuring compliance with GMP standards, maintaining accurate documentation, and leading production staff to achieve output and quality targets.

Key Responsibilities

• Supervise solid dosage production activities including granulation, compression, coating, encapsulation, and packing.
• Ensure production activities comply with approved Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs).
• Monitor production schedules to meet output targets while minimizing downtime and waste.
• Ensure proper line clearance before and after each batch.
• Enforce compliance with Good Manufacturing Practices (GMP), safety, and quality standards.
• Ensure accurate completion of production records, logs, and reports.
• Report deviations, non-conformances, and equipment malfunctions promptly.
• Support Quality Assurance (QA) during in-process checks, audits, and inspections.
• Supervise, train, and motivate production operators and line staff.
• Allocate duties, manage shifts, and ensure adequate manpower on the solid line.
• Enforce discipline, safety compliance, and proper use of Personal Protective Equipment (PPE).
• Identify training needs and support staff development initiatives.
• Ensure proper operation, cleaning, and routine maintenance of production equipment.
• Coordinate with Engineering/Maintenance teams for preventive and corrective maintenance.
• Monitor process parameters to ensure product consistency and production efficiency.
• Maintain good housekeeping and 5S standards within the production area.
• Ensure proper handling and disposal of waste materials in line with safety and environmental guidelines.

Requirements & Qualifications

• HND or Bachelor’s degree in a relevant science or engineering discipline.
• 3–5 years’ experience in pharmaceutical solid dosage manufacturing.
• Strong knowledge of GMP, SOPs, and pharmaceutical production processes.
• Experience supervising production teams in a regulated environment.
• Good leadership, communication, and documentation skills.
• Strong attention to detail and ability to work under pressure.

Application Closing Date
31st January, 2026.

How to Apply
Interested and qualified candidates should:
Click here to apply online