Salary
≈ $17k – $40k per year (Estimated)
Location
In office (Paianía)
Employment
Full-Time
Confirmed on the employer's own hiring board on Nov 2, 2026. First seen by Alion on Oct 27, 2026. Lavipharm scores A on the Alion truth index.
Overview
Company
Impact
Profile match
Lavipharm is a dynamic, international healthcare company driven by creativity and innovation, always striving to provide access to improved healthcare solutions.
Lavipharm is seeking a Supervisor of FP, based in Athens, who will be responsible for supervising the day-to-day testing and release-support activities of the FP QC team, ensuring analyses are performed accurately, on time, and in full compliance with cGMP, Good Documentation Practices (GDP) and data integrity requirements.
Requirements
- Supervises and coordinates the daily activities of the Semi-Finished, FP Release and Stability Programs, Process, Analytical and Cleaning Validation analysis ensuring workload is prioritized to meet business objectives and defined timelines
- Trains, develops and performs performance reviews of QC FP team members, ensuring they are equipped with the skills and knowledge to perform their roles effectively
- Collaborates with QA, production, supply chain, RA, RnD and engineering teams to resolve quality-related issues and enhance product quality
- Leads team Problem solving and troubleshooting sessions towards continuous improvement of QC Operations in FP
- Monitors compliance of the FP team to all procedures, specifications, GMP and safety rules of the QC Laboratory
- Champions Good Documentation Practices (GDP) and data integrity (ALCOA+) principles across the FP QC team, ensuring records are accurate, legible, contemporaneous, original and attributable
- Leads as required and approves the investigation of OOS/OOT results
- Reviews & Approves CoAs
- Hosts and supports internal and external audits and regulatory inspections related to FP QC, ensuring timely and accurate responses
- Owns and progresses deviations and change controls related to FP testing through to closure
- Ensures instruments and computerized systems used for FP testing are properly qualified, maintained, calibrated and in proper operation, in accordance with applicable procedures
Requirements
- BSc in Chemistry, Postgraduate degree in Pharmaceutical Science or related field is a plus
- At least 10 years' experience in the Pharma industry within Quality Control operations, including exposure to FP testing
- At Least 3 years in supervisory roles in QC Operations
- Advanced Knowledge of the English language
- Computer Literacy (MS Office, ERP System)
- eQMS/eDMS experience will be considered a plus
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