Our Mass Recruitment team, in partnership with Accord, a leading pharmaceutical company, is seeking talented Senior 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).
• 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
• 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
• At least 3 years work experience in a QC laboratory of a pharmaceutical organization
• Experience in analytical methods and in particular HPLC
• Attention to detail and a methodical, investigative and inquisitive mind
• Time management and organizational skills
• Excellent oral and written communication
• Fluent in Greek & English