Question
2-5

Officer, QA

4/19/2026

The QA Officer will perform physical and chemical analyses while ensuring strict adherence to Good Manufacturing Practices (GMP) within the production workshop. They are responsible for conducting in-process controls, managing batch records, and monitoring environmental conditions to ensure product conformity.

Working Hours

40 hours/week

Company Size

11-50 employees

Language

English

Visa Sponsorship

No

About The Company

No description available for this Company.

About the Role

Location: Algiers, Algeria

Job Type: Full-time

 

About Us:

For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.

As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.

Description:

We are looking for a talented Officer, QA (Oncology) to join us. At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We’re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.

If you want to be part of a team that cares about impact, this is the place for you.

Main Responsibilities:

  • Perform physical and chemical analyses as part of analytical research activities.
  • Ensure compliance with Good Manufacturing Practices (GMP) within the production workshop
  • Perform in-process checks and controls on products during manufacturing
  • Ensure product conformity with technical and documentation specifications
  • Follow manufacturing orders and packaging standards
  • Manage waste generated during the production process in accordance with current regulations
  • Carry out necessary sampling during manufacturing and packaging stages
  • Review and close batch records
  • Collect reference samples for the ANPP
  • Participate in the acceptance of finished and semi-finished products
  • Monitor temperature and humidity in the relevant areas

Required Skills:

  • Ability to perform in-process controls and interpret results accurately
  • Familiarity with batch record review and documentation procedures
  • Knowledge of sampling techniques and quality control processes
  • Understanding of hygiene, safety, and environmental regulations
  • Ability to work in a regulated and controlled environment
  • Good communication and teamwork skills

Academic Background and Knowledge:

  • Degree in Pharmacy or Engineering (Biology, Chemistry, or Process Engineering)
  • At least 2 years of experience in a similar role (preferably in the pharmaceutical or cosmetics industry)
  • Strong attention to detail, organizational skills, and a sense of responsibility
Key Skills
Quality AssuranceGood Manufacturing PracticesAnalytical ResearchIn-process ControlsBatch Record ReviewSampling TechniquesQuality ControlHygiene RegulationsSafety RegulationsEnvironmental RegulationsCommunicationTeamworkDocumentationChemical AnalysisPhysical Analysis
Categories
HealthcareManufacturingScience & ResearchEngineering
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