Production Manager 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 Manager

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

Job Description

• The Production Manager is responsible for overseeing pharmaceutical manufacturing operations, ensuring strict compliance with Good Manufacturing Practices (GMP), and delivering efficient, high-quality production output.
• The role also involves team leadership, process optimization, and regulatory compliance.

Key Responsibilities
Production Operations:

• Plan and execute daily, weekly, and monthly production schedules
• Ensure adherence to approved Master Formula and Batch Manufacturing Record (BMR) instructions
• Ensure real-time and accurate documentation of batch manufacturing activities
• Oversee line clearance and changeover procedures
• Monitor production yields and investigate variances.

GMP & Documentation Compliance:

• Ensure zero undocumented deviations
• Review completed BMRs before submission to Quality Assurance (QA)
• Enforce ALCOA+ data integrity principles
• Ensure strict compliance with Standard Operating Procedures (SOPs)
• Support QA in deviation investigations and CAPA implementation

Validation & Qualification Support:

• Participate in process validation, cleaning validation, and hold-time studies
• Ensure production readiness for IQ/OQ/PQ activities
• Collaborate with the Engineering and QA teams on validation schedules

Personnel Management:

• Supervise Production Supervisors and Operators
• Identify skill gaps and coordinate GMP training programs
• Maintain discipline and accountability on the production floor
• Promote a strong safety culture and zero-accident environment

Continuous Improvement:

• Improve Overall Equipment Effectiveness (OEE) and reduce downtime
• Optimize material usage and minimize wastage
• Drive cost control initiatives without compromising quality and compliance.

Requirements

• B.Pharm (mandatory)
• 7–10 years of manufacturing experience
• At least 5 years in a pharmaceutical production environment
• Minimum 3 years in a supervisory or managerial role
• Strong knowledge of GMP, ALCOA+, and regulatory requirements
• Excellent leadership and team management skills
• Strong problem-solving and analytical abilities.

Application Closing Date
27th March, 2026.