QA Officer

Hikma Pharmaceuticals

QA Officer role ensuring compliance in injectable manufacturing operations at Hikma Pharmaceuticals. Conducting QA investigations and monitoring GMP adherence with a focus on team collaboration.

Posted 7/29/2026full-timeCasablanca • 🇲🇦 MoroccoMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Quality Assurance activities, including compliance with GMP and regulatory requirements, while effectively communicating and building awareness in both French and English. Strong analytical skills and attention to detail are essential for conducting thorough investigations and ensuring quality standards in injectable manufacturing.

Highest-signal resume keywords

Quality AssuranceGMP ComplianceAnalytical SkillsBilingual CommunicationAttention to Detail

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Quality Assurance ActivitiesGMP KnowledgeData RecordingAcceptance TestingIn-Process ControlsInvestigationsCorrective ActionsDocumentation PracticesEnvironmental MonitoringLine Clearance

Soft Skills

Strong CommunicationAwareness-BuildingQuality-Focused Mindset

Industry Keywords

Injectable ManufacturingPackaging AreasRegulatory RequirementsProduction AreasPersonnel HygieneReinforced InspectionsFinished-Product Sampling

About the role

Key responsibilities & impact

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.

Requirements

What you’ll need

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.

Benefits

Comp & perks

Full-time 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score