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Quality Systems Specialist

ID:  2527
Date of Posting:  May 26, 2026
Business Area:  Quality
Job Type:  Direct Employee
On site / Remote / Hybrid:  On Site
Hub Office: 

Çerkezköy, TR

Territory: 
Full-Time or Part-Time:  Full Time
Seniority:  Entry level

At Recordati, we are united by a clear purpose: unlocking the full potential of life. With a century of history behind us, we are building the next chapter of our journey, continuing to grow while keeping patients at the centre of all we do.

What drives us is a shared belief that health, and the opportunity to live life to the full, should be within reach for everyone. This brings energy to our work, shaping how we support each other and show up every day. Our values – Better Together, Never Settle and Always Deliver – reflect this mindset, helping us to keep improving and make a meaningful difference.

Above all, these values bring to life our promise to everyone at Recordati, you can unlock your full potential. We know that people thrive when they can be themselves, are trusted and supported, and are given the opportunity to grow and make a meaningful contribution.

Are you ready to unlock your full potential?

Job Purpose

Key Responsibilities

 

Key Responsibilities:

 

  • Plan, coordinate and ensure delivery of GMP and Quality System training for personnel,
  • Track and follow up on GMP / Quality System inspections conducted by the Ministry of Health and international regulatory authorities; prepare, implement, and maintain CAPA action plans,
  • Prepare and communicate internal audit plans in collaboration with relevant departments,
  • Manage and monitor activities related to CAPA and Change Control processes,
  • Participate in Supplier Audits for packaging and primary packaging materials together with responsible stakeholders,
  • Provide cross-functional support within the Quality Assurance department as needed (Deviations, Change Control, Annual Product Quality Reviews, etc.).

Required Education

Required Skills and Experience

 

Qualifications:

  • Bachelor’s degree in Chemistry, Chemical Engineering, or a related scientific discipline,
  • 3-4+ years of Quality Assurance experience in the pharmaceutical industry,
  • Strong knowledge of GMP regulations and quality documentation systems,
  • Proficient in Microsoft Office applications,
  • Analytical, systematic, and results-oriented mindset with strong teamwork and communication skills,
  • Fluent or professionally proficient English preferred,
  • Completion of military service required for male candidates,
  • Residing in or willing to relocate to Çerkezköy, Kapaklı, Çorlu or Ergene within a short time frame.

Technical Competencies

Required Behaviours and Competencies

Required Languages

Travel required in %

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.

Apply now »