Our Mass Recruitment team, in partnership with Accord, a leading pharmaceutical company, is
seeking talented QC Analysts to join a dynamic and innovative team.

Key Responsibilities: 

• Ensuring cGMP and cGLP compliance.
• 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).
• Sampling and testing: RM, PM, FP and stability samples
• Stability sample management and stability protocol preparation.
• Daily calibration and verification checks for QC instruments.
• Impurity and standard managements.
• Daily monitoring of data loggers and recording.
• Management of HPLC/GC Columns
• Procurement of Laboratory chemicals & consumables.
• Follows and complies to all good practices (GMP, GDP), to the Quality Management System, regulatory requirements, internal processes and procedures, company guidelines, the corporate governance code, the Health Safety and Environment (EHS) procedures and good practices and all company policies and regulations, and actively contributes to their improvement.
• Ensures and protects data integrity in every action.
• Undertakes any other project or responsibility that is assigned by the company, within the broader scope of the position’s responsibilities.

Essential Requirements: 

• Bachelor Degree in Chemistry, Biology, Health Sciences, Food Technology, Pharmacy, Chemical engineer or any other relevant field
• Desirable work experience in a QC laboratory of a pharmaceutical organization
• Attention to detail and a methodical, investigative and inquisitive mind
• Time management and organizational skills
• Excellent oral and written communication
• Fluent in Greek & English