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  • Posted: Jan 5, 2026
    Deadline: Jan 30, 2026
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  • We work at the critical intersection where innovations that save and sustain lives meet the physicians, nurses and pharmacists who make it happen. We are committed to improving outcomes for patients, and helping our partners meet the evolving challenges and opportunities in healthcare around the world. Learn more about our diverse specialties.
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    Production Manager (IVF Plant)

    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

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified candidates should forward their CV to: jobs@delepharma.com using the position as subject of email.

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