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
No description available for this Company.
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
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