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This is a great opportunity for a QC professional who is looking to develop their skills and evolve professionally within a multinational pharmaceutical company.
Job Responsibility:
GLP document preparation e.g. SOPs, Specification and Method of Analysis, Certificate of Analysis etc.
Good documentation practices and record keeping of all GMP documents / logs. (RM, PM, IP, FP sampling and testing)
Record and review GMP data, monitor and evaluate QC systems and equipment, recommend improvements to procedures, and revise GMP documentation as required
Calibrate, monitor, maintain and evaluate systems and equipment (i.e. water systems, environmental chambers, analytical instrument/equipment)
Direct troubleshooting of routine problems of limited scope and complexity following established procedures
Conclude the analyses by generating accurate, correct and timely results via the corporate laboratory software
Mentor junior Analysts on testing, troubleshooting and Lab related items
Undertake investigations during any incidents/deviations/change controls/OOS
Monitor all laboratory-related consumables
Support regulatory, third party, and internal audits when required
Review technical reports, summaries and protocols
Ensure compliance with all cGMP standards, safety, and environmental regulations and company SOPs
Record all results in ERP/SAP
Requirements:
At least 3 years of relevant working experience
Bachelor's degree or equivalent in Life Sciences (Chemistry, Biology, Pharmacy or similar)
Strong knowledge of quality control methodologies and techniques
Fluency in Greek and English language (oral and written)
A highly organized mindset with excellent attention to detail
Excellent knowledge of laboratories' equipment, software and GMP processes
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