Quality Assurance Supervisor at Orange Drugs Limited

Posted on: Mon 18-09-2023

Orange Group is an innovative Fast Moving Consumer Goods company based out of Nigeria, with a footprint that stretches across West Africa in three key segments; Pharmaceuticals, Personal Care, Food and Beverage

We are recruiting to fill the position below:

Job Title: Quality Assurance Supervisor

Location: Lagos

Job Type: Full Time

Key Responsibilities

  • Provide concise conclusions and summaries of test results for samples, including products, materials, stability testing, temperature mapping, and environmental monitoring.
  • Oversee validation and qualification activities.
  • Collaborate with Materials department personnel to establish requirements for external suppliers.
  • Monitor performance by collecting relevant data and generating statistical reports.
  • Identify pertinent quality-related training needs and assist the Quality Assurance Manager in delivering training.
  • Establish clear quality practices and standards for all personnel.
  • Develop the annual validation master plan and ensure its implementation.
  • Ensure that equipment changes undergo necessary risk assessment.
  • Conduct required risk assessments and monitor mitigation plans for identified hazards.
  • Initiate CAPA forms for deviations as needed.
  • Regularly update and monitor the CAPA tracker.
  • Keep abreast of updates from WHO/ICH/NAFDAC websites, including WHOPIRs, Regulations, and Pharmacopoeias on a quarterly basis.

Job Factors

  • Supervision of Documentation Officer, Validation Officer, and In-Process Control Officers.
  • Internal/External Relationships:
  • Engage with Production, Warehouse, Sales and Marketing, Human Resources/Admin, Business Support team, and Engineering personnel on matters concerning factory GMP operations and Regulatory affairs.
  • Collaborate with Materials Manager regarding materials management.


  • Bachelor's Degree in Industrial Chemistry / Biochemistry / Pharmacy / Pharmaceutical Sciences.
  • Minimum of 3 years of experience in Pharmaceutical Manufacturing.
  • Demonstrated high level of integrity, expertise in GMP, Chemistry, and Pharmaceutical technology, and the ability to work with minimal supervision.
  • Perform duties within agreed specifications and timelines.

Application Closing Date

Not Specified.

How to Apply

Interested and qualified candidates should send their CV to: [email protected] using "Quality Assurance Supervisor" as the subject of the mail.