Quality Assurance Officer at Lavipharm

Paiania, Attica, Greece -

Full Time

Start Date

Immediate

Expiry Date

17 May, 26

Salary

0.0

Posted On

16 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality System Implementation, Quality Assurance Audits, Process Monitoring, Corrective Measures, Regulatory Oversight, Documentation Management, Product Quality Review, Stability Studies, Standard Operating Procedures, Validation Protocols, GMP Compliance, Batch Documentation Review, Quality Complaints Investigation, Statistical Evaluation, Change Management, Corrective And Preventive Actions

Industry

Pharmaceutical Manufacturing

Description

Lavipharm is seeking a Quality Assurance Officer, based in Athens who will be responsible for the implementation of the quality system, conducting quality assurance audits, monitoring and recording results from processes and procedures, as well as, taking corrective measures if any deviation is found. Responsibilities Compliance & Regulatory Oversight • Follows international standards and complies with regulations Documentation & Record Management • Issues the annual "Product Quality Review" of all products • Follows up the monthly stability studies of the QC Department and issues the relevant stability protocols and reports • Ensures standard operating procedures and manufacturing documentation for all products is kept up to date • Issues Process and Cleaning Validation Protocols, in accordance with the applicable Guidelines • Evaluates the Plant and Laboratories for compliance with GMPs standards • Reviews production batch documentation • Issues, revises and reviews Standard Operating Procedures (SOPs) for the QMS system • Issues, follows up and archives investigation of quality complaints with customers and suppliers • Implements statistical evaluation studies for product release, shelf life and yield specifications • Issues, follows up and archives investigation of quality deviations with the collaboration of the impacted department • Issues, prepares, archives and follows up the change management system • Issues, follows up and archives corrective and preventive actions • Implements a thorough training program for all employees in the site Bachelor degree in Chemistry, Biochemistry, Analytical Chemistry or other relevant field At least 3 years experience in Quality manufacturing/systems preferably in Human Pharma Industry Excellent Knowledge of the English language Computer Literacy (MS Office etc)

Responsibilities

The Quality Assurance Officer will be responsible for implementing the quality system, conducting audits, monitoring processes, and taking corrective action for any deviations found. Key duties include managing documentation, issuing reviews and protocols, and ensuring compliance with GMP standards.