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Are you ready to play a vital role in ensuring strong product quality in a pharmaceutical manufacturing environment? Proclinical is seeking a QC Analyst to support quality control operations within the pharmaceutical manufacturing sector. In this role, you will ensure that all materials are tested according to agreed specifications and procedures while maintaining compliance with industry standards. This position requires a focus on safety, quality, and continuous improvement, with opportunities to contribute to audits, inspections, and technology transfer projects.
Job Responsibility:
Test all materials in accordance with agreed specifications and procedures
Qualify laboratory equipment, including URS, IQ, OQ, and PQ processes
Maintain and calibrate laboratory equipment following approved procedures
Manage laboratory Quality Systems and Quality Management Systems
Draft Standard Operating Procedures (SOPs) under supervision
Support internal and external audit processes and schedules
Assist in preparing for and hosting competent authority inspections
Investigate deviations and implement corrective and preventive actions (CAPAs)
Contribute to technology transfer projects, particularly QC aspects
Implement and manage change control activities
Collect data for Product Quality Reviews (PQRs) and Quality Assurance Performance Indicators
Manage stability programs and associated activities
Perform other duties as requested by the QC Head
Requirements:
Strong knowledge of Quality Control, Quality Assurance, GMP, and regulatory compliance
Ability to interpret complex data and present findings effectively
Proficiency in computer applications such as Word, Excel, and PowerPoint
Familiarity with GMP guidelines and regulations
Excellent problem-solving, decision-making, and time management skills