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Quality Assurance Manager

Juhel Nigeria Limited
Enugu Posted Oct 6, 2026
On-site

About this role

Juhel Nigeria Limited

At Juhel Nigeria Limited, we save lives by increasing access to quality essential medicines. A private company founded in 1987, Juhel Nigeria Limited is one of the pioneer pharmaceutical manufacturers in West Africa. With over 150 registered products across multiple formulations and therapeutic areas from our multiple factories, we are one of the largest pharmaceutical manufacturers in West Africa.

We are recruiting to fill the position below:

Quality Assurance Manager

Location: Enugu

Contract type: Long-term

Experience required: 4 years (pharmaceutical industry)

Main Responsibilities (not exhaustive)

  • Design, implement, and maintain the facility’s Quality Management System, ensuring all operational processes align with national regulatory standards (such as NAFDAC, SON).
  • Review and approve Standard Operating Procedures (SOPs), batch manufacturing records, specifications, and validation protocols to uphold data integrity and ensure that it is duly followed by staff.
  • Lead investigations into manufacturing or laboratory deviations, out-of-specification (OOS) results, and customer complaints using root cause analysis, followed by implementing Corrective and Preventive Actions (CAPAs).
  • Plan and execute internal self-inspections, qualify external raw material suppliers and contractors, and lead the facility during official regulatory agency inspections.
  • Oversee quality approval for the qualification and validation of manufacturing equipment, computer systems, and critical plant processes (IQ, OQ, PQ).
  • Conduct final reviews of production data and authorize the disposition or market release of pharmaceutical batches.
  • Manage the Quality department staff and ensure that they work effectively and efficiently.
  • Manage comprehensive GMP training matrices for personnel across departments to maintain a high standard of regulatory awareness and competency.

Requirements

Professional requirements (minimum):

  • Bachelor’s Degree, B.Pharm, or HND
  • Preferred- BSc / HND / B.Pharm, Pharmacy, Chemistry, Industrial chemistry, Biochemistry, Microbiology, Biotechnology, Chemical Engineering.

Language required (minimum):

  • English Language

Software knowledge required (minimum):

  • Google Docs, Google Sheets, Google Slides
  • OR its equivalents (e.g. Microsoft Word, Excel and Powerpoint etc.)

Personal requirements:

  • Strong written and verbal communication skills
  • Excellent organisational and planning skills
  • Good understanding of cGMP and Quality Management System
  • Good problem solving skills.
  • Strong integrity
  • Creative, Flexible, Agile
  • Self-driven, Initiative, Proactive
  • Detail oriented & analytical

Application Closing Date

16th October, 2026.

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