PharmaPlot is a fast-growing Greek company focused on the development, out-licensing and supply of high-quality generic medicinal products and “value-added” medicines. Our portfolio contains solid dosage forms (tablets & capsules), injectables, oral solutions and suspensions. We offer robust supply chains and a full range of services covering all stages of the pharmaceutical value chain, from Product Development to Regulatory Approval and Life Cycle Management.

Currently, given its expanding business, PharmaPlot is recruiting a Quality Assurance Officer, based on the company’s GMP premises in Gerakas area, Athens, Greece.  

Main Responsibilities:

• Contributes to the company’s “global” Quality Management System (QMS) maintenance (GMP, GDP requirements, API registration requirements, controlled documents management, Validation Master plan update, periodic review, Site Master File maintenance, Compendial review logbooks issuance etc.).
• Participates in the review process of product-related documents (e.g. protocol and reports, Certificates of Analysis, Analytical Procedures, Product Quality Reviews etc.).
• Contributes to the management of the Quality Events (Deviations, OOS/OOT results), CAPAs, Risk Assessments and Change Controls either internally raised (GMP & GDP activities of the company) or externally raised (e.g. by the subcontracted CMOs etc.).
• Contributes to the suppliers’, subcontractors’ (API suppliers, CMOs, laboratories, warehouses, etc.) and clients’ qualification and to the maintenance of the related databases (e.g. qualification records, Quality Technical Agreements, Licenses etc.).
• Participates in internal (and external, when applicable) audits in the frame of the evaluation of internal performance with regards to the conformity with the company’s Policies, QMS and applicable regulations and in the frame of suppliers’ qualification requirements.
• Participates in the preparation of the company for accepting audits and inspections by third parties (i.e. clients and competent Authorities).
• Contributes to the control and maintenance of the various system databases, logs and inventories as well as KPIs.
• Archiving of the company’s Quality documentation and relevant records.

Education Requirements:

• Pharmacy bachelor’s degree
• MSc in Analytical Chemistry, Pharmaceutical Analysis or similar field is a plus
• Excellent knowledge of the English language (CEFR Level B2)
• Basic knowledge of Microsoft Office applications

Other Requirements:  

• Practical experience in a GMP environment is a plus
• Analytical & critical thinking ability
• Ability to prioritize & organizational skills
• Team-working & problem-solving skills
• Good writing skills
• Attention to detail

Company offers:

• Competitive salary
• Friendly corporate culture
• Private Health Insurance
• Training on GMP & GDP principles and relevant fields
• Scientific working environment with strongly motivating character