Officer, QA at Hikma Pharmaceuticals PLC

Staoueli, Algiers, Algeria -

Full Time

Start Date

Immediate

Expiry Date

18 Jul, 26

Salary

0.0

Posted On

19 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Good Manufacturing Practices, Analytical Research, In-process Controls, Batch Record Review, Sampling Techniques, Quality Control, Hygiene Regulations, Safety Regulations, Environmental Regulations, Communication, Teamwork, Documentation, Chemical Analysis, Physical Analysis

Industry

Description

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

Responsibilities

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.