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Title:  Officer, QA

Description: 

Location: Casablanca, Morocco

Job Type: Full-time

Hashtag: #LI-MM1

 

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 QA Officer 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.

 

Key Responsibilities:

 

  • Conduct daily QA walkthroughs in the injectable manufacturing and packaging areas.
  • Verify compliance with GMP, good documentation practices, and real-time data recording.
  • Check the condition of production areas, equipment, materials, and environmental conditions.
  • Monitor personnel hygiene and ensure that line clearance activities are properly completed.
  • Prepare QA walkthrough reports and follow up on the implementation and effectiveness of corrective actions.
  • Perform acceptance tests at the different manufacturing stages and accurately record the results.
  • Participate in in-process controls, reinforced inspections, and finished-product sampling.
  • Conduct investigations related to deviations within the Injectables Department.

Qualifications:

We are looking for candidates whose experience and skills align closely with the qualifications outlined below:

 

  • Technical or scientific educational background.
  • Good knowledge of Quality Assurance activities and requirements.
  • Good understanding of GMP and applicable regulatory requirements.
  • Strong communication and awareness-building skills.
  • Good command of French and English.
  • Strong attention to detail, analytical skills, and a quality-focused mindset.
Location: 

Casablanca, MA

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