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Fagron

quality lead

Jul 29, 2026 · Fagron

Τρίκαλα·Jul 29, 2026
ΤρίκαλαOn SiteΒιομηχανική ΠαραγωγήPermanentFull Time
JOBILY AI SUMMARY

What you'll do

  • Lead and mentor the Quality team to achieve quality objectives
  • Maintain and continuously improve Quality Management System (QMS)
  • Develop, implement, and maintain quality management systems, processes, and procedures
  • Monitor product or service quality throughout the production or delivery lifecycle
  • Conduct root cause analysis for quality issues and implement corrective and preventive actions (CAPA)
  • Review quality metrics, prepare reports, and present findings to management
  • Ensure compliance with GMP and regulatory guidelines
  • Plan and conduct internal quality audits
  • Collaborate with production, procurement, operations, and customer service teams to resolve quality issues and complaints
  • Identify opportunities for process improvement using quality tools
  • Manage customer complaints, non-conformance reports, and corrective action tracking
  • Develop and deliver quality training programs for employees
  • Drive a culture of continuous improvement and quality excellence
  • Prepare the site for regulatory inspections and customer audits
  • Support responses to audit observations and implement corrective actions
  • Oversee investigations related to deviations, non-conformances, customer complaints, and OOS results
  • Review and approve Corrective and Preventive Actions (CAPA) for timely and effective closure
  • Manage change control activities and assess quality risks
  • Review and approve SOPs, batch manufacturing records, validation documents, protocols, and reports
  • Review and approve GMP documentation, validation protocols, qualification reports, and quality records

Key requirements

  • 2+ years' experience
  • Quality Management System (QMS) and related documentation
  • Corrective and Preventive Actions (CAPA) and Root Cause Analysis
  • Compliance with Good Manufacturing Practice (GMP) and Regulatory Compliance
  • Internal Quality Audits and Quality Metrics and Reporting
  • Customer Complaint Management and Change Control Management
  • Training Program Development and Delivery
  • Equipment Qualification, Process Validation, Cleaning Validation, and Computerized System Validation
  • Pharmacy / Chemistry / Biology / Chemical Engineering

Benefits

  • At Fagron, you’ll find plenty of chances to grow — both personally and professionally.
  • We work in an open, dynamic environment where your ideas and talents can shine.
  • We’re proud to be an equal opportunity employer.
  • Diversity makes us stronger, and we’re committed to creating an inclusive workplace where everyone feels welcome.

About the job

- Lead and mentor the Quality  team to achieve quality objectives
- Maintain and continuously improve Quality Management System (QMS)
- Develop, implement, and maintain quality management systems, processes, and procedures
- Monitor product or service quality throughout the production or delivery lifecycle
- Conduct root cause analysis for quality issues and implement corrective and preventive actions (CAPA)
- Review quality metrics, prepare reports, and present findings to management
- Ensure compliance with applicable industry standards, customer requirements, and regulatory guidelines according to GMP
- Plan and conduct internal quality audits
- Collaborate with production, procurement, operations, and customer service teams to resolve quality issues and complaints
- Identify opportunities for process improvement using quality tools 
- Manage customer complaints, non-conformance reports, and corrective action tracking
- Develop and deliver quality training programs for employees
- Drive a culture of continuous improvement and quality excellence
- Prepare the site for regulatory inspections and customer audits
- Ensure compliance with regulatory agencies and other applicable health authorities
- Support responses to audit observations and implementation of corrective actions
- Oversee investigations related to deviations, non-conformances, customer complaints, and out-of-specification (OOS) results
- Review and approve Corrective and Preventive Actions (CAPA) to ensure timely and effective closure
- Manage change control activities and assess quality risks associated with process or system changes
- Ensure timely review and approval of Standard Operating Procedures (SOPs), batch manufacturing records (BMRs), validation documents, protocols, and reports
- Review and approve GMP documentation, validation protocols, qualification reports, and quality records
- Perform equipment qualification, process validation, cleaning validation, and computerized system validation activities

Set yourself apart

You possess the following qualifications, background and abilities:

- Bachelor’s degree (Pharmacy, Chemistry, Biology, Chemical Engineering)
- 2+ years experience is preferable 
- Excellent written and verbal communication skills 
- Fluent in English

What's on offer?

At Fagron, you’ll find plenty of chances to grow — both personally and professionally. We work in an open, dynamic environment where your ideas and talents can shine.

We’re proud to be an equal opportunity employer. 🌍 Diversity makes us stronger, and we’re committed to creating an inclusive workplace where everyone feels welcome.

About the company

Fagron is the world’s leading personalized medicine company and offers prescribers, pharmacists and patients the broadest possible range of therapeutic options. As the market leader, we act locally and think globally. By recruiting the best minds, we aim to strengthen our leading position.

Workplace
On Site
Sector
Βιομηχανική Παραγωγή
Employment Type
Permanent
Work Time
Full Time

About the company

Fagron is the world’s leading personalized medicine company and offers prescribers, pharmacists and patients the broadest possible range of therapeutic options. As the market leader, we act locally and think globally. By recruiting the best minds, we aim to strengthen our leading position.