Overview

Responsibilities:
  • Ensure compliance with quality standards, internal procedures, and ISO 17025 requirements
  • Participate in the implementation, maintenance, and continuous improvement of the Quality Management System (QMS ISO 9001)
  • Prepare, review, and maintain quality-related documentation (SOPs, protocols, reports, records)
  • Perform analytical testing in the laboratory using relevant analytical equipment
  • Operate, maintain, and document work with laboratory instruments in accordance with approved procedures
  • Support audits and inspections when required
Required Qualifications:
  • Higher education in Chemistry, Pharmaceutical Sciences, or a related field
  • Experience or strong interest in Quality Assurance and analytical laboratory work
  • Practical experience with analytical laboratory instruments (e.g. HPLC, UV, etc.)
  • Good understanding of quality systems and laboratory documentation practices
  • Good command of English (written and spoken)
Note:

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