Validation Executive

Sanovel İlaç

• Graduated from Chemistry, Chemical Engineering and Pharmacy,
• At least 8 years of validation experience in pharmaceutical industry,
• Knowledge of GMP Quality Standards
• Strong commitment to compatibility, scientific quality and integrity,
• Knowledge and understanding of global regulatory procedures,
• Leader in terms of performance, owning learning agility,
• Having a high sense of empathy and being curious about everything new and unusual,
• Managing relationships and responsibilities with collaboration,
• Exellent command of English with Critical Negotiations skills,
• Operations Management and Execution,
• Collaborating across boundaries,
• Residence in Çorlu, Çerkezköy or Silivri.

JOB DESCRIPTION

• Management of Cleaning and Process validation program in the company.
• Validation and Administration of GxP critical Computerized Systems.
• Management of Data Integrity Compliance strategy in the company.
• Monitoring of Current Regulation, Guidelines and Standards and update the quality systen accordingly.
• Management of process control and process improvement activities.
• Support on validation related activities for the design, commissioning, qualification and continued validation maintenance of all equipment and utilities.
• Performing GAP analysis to meet Regulatory Expectations.
• Taking an active role in Internal and External Quality audits.
• Work closely with the business partners on Process Control and Quality aspects.
• Oversight of all production & testing activities, ensures compliance with cGxP.