Production Pharmacist (Infusion Plant) at Dele Pharmaceutical

Dele Pharmaceutical Group proudly stands as a leading force in Nigeria’s healthcare landscape. We are not just a conglomerate; we are a symphony of expertise, harmonizing the strengths of HMA Medical Ltd and Ayo-Ayodele Pharmaceutical Chemist Nigeria Ltd, to deliver quality-compliant medical products that exceed customer expectations.

Dele Pharmaceutical Group is more than just a manufacturer; we are a partner in healthcare. We are the quiet hero behind every successful procedure, the silent guardian of patient comfort, and the unwavering advocate for quality care. With every product, we deliver a promise of excellence, a commitment to integrity, and a deep-seated belief in the power of healthcare to heal, to empower and to inspire. We are relentlessly committed to continually improving the quality of healthcare in Nigeria and beyond.

We are recruiting to fill the position below:

Job Title: Production Pharmacist (Infusion Plant)

Location: Ilorin, Kwara
Employment Type: Full-time

Key Responsibilities
Production Planning & Control:

• Plan and manage daily, weekly, and monthly production schedules for IV fluids.
• Ensure optimal utilization of manpower, machines, materials, and utilities.
• Monitor production output against targets and take corrective actions where necessary.
• Minimize downtime, wastage, and production losses.

GMP & Regulatory Compliance:

• Ensure full compliance with cGMP, WHO guidelines, NAFDAC regulations, and SOPs.
• Participate in internal, external, and regulatory inspections and audits.
• Implement and sustain GMP culture across all production operations.
• Ensure proper documentation of batch manufacturing records (BMRs).

Quality Assurance Collaboration:

• Work closely with Quality Assurance and Quality Control to ensure product quality.
• Investigate deviations, OOS, OOT, and non-conformances related to production.
• Support CAPA implementation and effectiveness reviews.
• Ensure line clearance and in-process controls are strictly adhered to.

Equipment & Facility Management:

• Ensure proper operation, cleaning, and maintenance of production equipment.
• Coordinate with Engineering/Maintenance for preventive and breakdown maintenance.
• Ensure validation status of equipment, processes, and utilities is maintained.
• Support qualification of new equipment and process improvements.

People Management & Training:

• Supervise, mentor, and evaluate production supervisors, line leaders, and operators.
• Identify training needs and ensure continuous GMP and technical training of staff.
• Enforce discipline, safety rules, and good housekeeping practices.
• Foster a culture of teamwork, accountability, and continuous improvement.

Safety, Health & Environment (SHE):

• Ensure compliance with safety, health, and environmental policies.
• Identify and mitigate production-related risks and hazards.
• Promote safe handling of raw materials, chemicals, and utilities.
• Ensure proper waste management and environmental controls.

Continuous Improvement:

• Drive process optimization, cost reduction, and productivity improvement initiatives.
• Implement Lean, 5S, and operational excellence practices.
• Participate in change control and process improvement projects.
• Support new product introductions and scale-up activities.

Key Performance Indicators (KPIs)

• Production output vs plan
• Batch rejection and deviation rates
• Equipment downtime
• GMP compliance score
• On-time batch release support
• Staff productivity and training completion.

Qualifications & Experience

• B.Pharm or Pharm.D Degree
• Registered Pharmacist with current license to practice or evidence of payment of Registration
• 3–5 years’ experience in pharmaceutical manufacturing, with at least 2 years in sterile/IV fluids production as an added advantage.
• Strong knowledge of aseptic processing, sterilization, WFI systems, and cleanroom operations.

Skills & Competencies:

• Strong leadership and people management skills.
• In-depth knowledge of sterile manufacturing and GMP.
• Excellent problem-solving and decision-making abilities.
• Good documentation and report-writing skills.
• Ability to work under pressure and meet production deadlines.
• Proficiency in MS Office and production reporting tools.

Application Closing Date
10th April, 2026.

Method of Application
Interested and qualified candidates should send their Applications to: jobs@delepharma.com using the job title as the subject of the mail.