quality assurance officer.

The benefits for the Quality Assurance Officer position include:

• opportunity for further career advancement.
• opportunity to work in a multinational and modern environment.
• competitive remuneration package. 
• corporate shuttle for transportation.

The ideal candidate for the Quality Assurance 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 comply 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.

The qualifications for the Quality Assurance Officer position include:

• Bachelor's or Master’s degree in 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.
• progressive technical/operational experience or equivalent.
• experience in pharmaceutical GMP.

• minimum 2 years of relevant experience

Does this role sounds like you or someone you know? We want to hear from you today. Apply online now!

Have some questions first? Call our office at +30 2166001308 and ask for Calypso Aronis. Otherwise, feel free to contact me at caronis@randstad.gr. 

Please note that for transparency and equity reasons, only those applications made online via our site will be assessed. After the screening of all the CVs received, we will only contact the candidates who meet the requirements of the job to arrange an interview. ​ All applications are considered strictly confidential.