qa operations officer.

The ideal candidate for the QA Operations Officer position will:

• Be responsible for handling and review of the Quality Deviations & Complaints and participates to the relevant investigations.
• Be responsible for the CAPA Management System in terms of updating the relevant database, performing evaluation, effectiveness check and closure of CAPAs.
• Be responsible for issuing the change controls and performing the follow up upon their completeness.
• Develop, update and review company processes (SOPs), contributing to the desired compliance with the requirements of GMP, ISO standards, customers, and state law.
• Issuance of process and packaging validation protocols and reports.
• Be responsible for performing batch record review and contribute to the quality release activities of final product.
• Issuance/ review of Product Quality Review reports.
• Be responsible for the training of personnel on quality topics.
• Participate in internal audits and identify non-conformities.
• Communicate with customers regarding quality issues.
• Follow and complie 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.
• Ensure and protect data integrity in every action.
• Undertake any other project or responsibility that is assigned by the company, within the broader scope of the position’s responsibilities.

1-2 years of experience

• Bachelors or Master’s degree in Chemical Engineer, Chemistry, Biology, Pharmacy or any relevant field.
• Attention to detail and a methodical, investigative and inquisitive mind
• Time management and organizational skills
• Excellent oral and written communication
• Fluent in Greek & English
• 1-2 years of progressive technical/operational leadership experience or equivalent.
• 1-2 Years of pharmaceutical cGMP experience