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Analyst, QC
Hikma PharmaceuticalsQC Analyst at Hikma Pharmaceuticals performing stability and validation analyses on pharmaceutical products. Involves manual and automated analyses, calibrating equipment, and preparing reagents.
About the role
Key responsibilities & impact- Performing stability, validation, raw materials, packaging materials, semi-finished and finished products analyses
- Conducting both manual and automated analyses
- Calibrating and adjusting laboratory equipment
- Preparing and storing reagents in accordance with established procedures
- Following the analysis schedule and comparing results against current standards
- Identifying anomalies and contributing to their resolution
- Recording and verifying results, and issuing analysis reports
- Proposing improvements in equipment organization
- Ensuring maintenance of workstations and providing technical training to new team members
Requirements
What you’ll need- Bachelor’s degree (Bac+3/4) in Chemistry, Pharmaceutical Quality Control/Analysis, or equivalent
- Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices)
- Familiarity with laboratory equipment and IT systems
- Ability to write procedures and reports
- Strong organizational skills and attention to detail
Benefits
Comp & perks- Access to a supportive culture of progress and belonging
- Opportunities for professional development
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
stability analysisvalidation analysisraw materials analysispackaging materials analysissemi-finished products analysisfinished products analysislaboratory equipment calibrationreagent preparationautomated analysismanual analysis
Soft Skills
organizational skillsattention to detailtechnical trainingproblem-solvingreport writing
Certifications
Bachelor’s degree in ChemistryBachelor’s degree in Pharmaceutical Quality Control/AnalysisGMP certificationGLP certification