Quality Control Analyst - Chemical Testing

About the role

As a Quality Control Analyst - Chemical Testing at Upjohn Saïdal Pharma, you will perform chemical and physical testing of raw materials, packaging materials, intermediate products and finished products to support manufacturing operations at the Algiers site. You will ensure that laboratory activities and their documentation comply with regulatory requirements, GMP, GLP, site procedures and Pfizer Quality Systems.

Key responsibilities

• Perform chemical and physical testing according to approved analytical methods, specifications and procedures
• Document laboratory activities accurately and contemporaneously, following Good Documentation Practices and Data Integrity requirements
• Review data generated by another qualified analyst when authorised to perform independent verification
• Take part in validation-batch testing, analytical method transfers, verification and validation
• Prepare, review and update technical documents such as methods, specifications, SOPs, protocols and reports
• Manage and monitor chemical reagents, reference standards, HPLC columns, consumables and glassware, and verify that equipment is within its approved status before use
• Support investigations of atypical results, deviations, OOS and OOT findings
• Maintain traceable analytical records, keep the work area clean (5S) and follow EHS procedures
• Complete training curricula and work with QA, production, supply, engineering and EHS teams

Required profile

• Bachelor's degree or equivalent in Chemistry, Analytical Chemistry, Pharmacy, Biology or a related scientific discipline
• Knowledge of GMP and GLP; familiarity with Data Integrity and ALCOA principles
• Previous experience in a pharmaceutical Quality Control laboratory
• Working knowledge of English and French

Required skills

• Practical experience with HPLC, UV-Visible spectrophotometry, dissolution testing and routine physicochemical tests
• Experience with analytical method transfer, verification or validation
• Familiarity with chromatographic data systems such as Empower and sample/material management systems
• Experience with 5S, continuous improvement or IMEx ways of working
• Good computer skills and ability to work in a team-based laboratory environment