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Pharmacist

Unknown · Ogun

Full TimeMidvia Telegram:Latest Jobs In Nigeria
Salary
Undisclosed
Location
Ogun
Posted
7 hours ago

Required skills

GMP complianceQuality assuranceQuality controlRegulatory complianceDocumentation and record managementPharmaceutical manufacturingRisk assessmentProblem-solvingAttention to detailMicrosoft OfficeCommunicationTeamwork

About the role

Pharmacist

Support the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products in a production environment. Ensure all products meet GMP standards, regulatory requirements, and company quality policies while promoting patient safety and product effectiveness.

Responsibilities

  • Ensure compliance with GMP, GDP, and applicable pharmaceutical regulations
  • Supervise and monitor manufacturing processes to meet quality standards
  • Review and approve batch manufacturing and packaging records
  • Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations
  • Monitor product stability and proper storage and handling of pharmaceutical products
  • Prepare and maintain accurate regulatory documentation
  • Participate in internal and external audits and implement corrective and preventive actions (CAPA)
  • Support product registration, licensing, and regulatory submissions
  • Investigate customer complaints, product defects, and recalls
  • Provide technical guidance and training to production and quality personnel
  • Collaborate with R&D, production, engineering, and regulatory teams
  • Ensure compliance with health, safety, and environmental policies
  • Stay updated with pharmaceutical regulation changes and industry best practices

Requirements

  • Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.)
  • Valid pharmacist license/registration with appropriate regulatory authority
  • Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems
  • Strong analytical and problem-solving skills
  • Excellent communication and teamwork abilities
  • Proficiency in Microsoft Office and pharmaceutical documentation systems
  • Experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs (preferred)

How to Apply

Interested and qualified candidates should send their CVs to: nosa@svnl.in using the job title as the subject of the email.

Application Closing Date: 31st July, 2026

📋 How to apply

Follow the application instructions in the How to Apply section of the role description above (email, phone, or link as posted by the employer).