Hikma Pharmaceuticals

QA Officer

Hikma Pharmaceuticals

full-time

Posted on:

Location Type: Office

Location: StaouéliAlgeria

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About the role

  • Perform physical and chemical analyses as part of analytical research activities.
  • Ensure compliance with Good Manufacturing Practices (GMP) within the production workshop.
  • Conduct in-process checks on products during manufacturing.
  • Ensure product compliance with technical and documentary specifications.
  • Follow manufacturing orders and packaging standards.
  • Manage waste generated during the production process in accordance with applicable regulations.
  • Collect necessary samples 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.

Requirements

  • 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 cosmetic industry)
  • Attention to detail, organizational skills, and a sense of responsibility
Benefits
  • None
  • Inclusion of people
  • Emphasis on well-being
Applicant Tracking System Keywords

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

Hard Skills & Tools
physical analysischemical analysisGood Manufacturing Practicesin-process checksbatch record reviewsample collectiontemperature monitoringhumidity monitoring
Soft Skills
attention to detailorganizational skillssense of responsibility
Certifications
degree in Pharmacydegree in Engineeringdegree in Biologydegree in Chemistrydegree in Process Engineering