Become part of Lubecafill

Are you looking for more than just an ordinary role – ready to take responsibility and drive meaningful progress?

At Lubecafill, you will experience a dynamic and internationally focused work environment – defined by agile decision-making, cutting-edge technologies and genuine opportunities for advancement. Join us in rethinking pharmaceutical processes with foresight, efficiency and long-term impact.

Mitarbeiterin bei der Lohnabfüllung - kreisförmiger Ausschnitt des Bildes


Why choose Lubecafill?

Respectful collaboration

Our corporate culture is defined by respect, transparency and international collaboration.

Technological Excellence

You will work with high-end equipment at the forefront of GMP-regulated pharmaceutical manufacturing.

Clear Communication

Openness and precision are key to efficient teamwork at all levels.

Career Opportunities

We actively promote talent through targeted training, project responsibility, and international development opportunities.

Global Perspective

As an export-oriented company with strong European ties, we think and act beyond borders.

Reliable Employer

Lubecafill stands for stability, long-term prospects, and a modern working environment with the highest standards.

Your future begins in a dynamic environment.

At Lubecafill, you will work in an environment that combines personal responsibility, team spirit, and technological innovation. Short decision-making paths, transparent communication, and state-of-the-art equipment create optimal conditions for you to fully realize your potential – structured, solution-oriented, and with an international focus.

About Lubecafill

Lubecafill stands for state-of-the-art pharmaceutical contract filling – with the ambition to redefine quality and efficiency.
At our site in Ergene / Tekirdağ, we are currently establishing an internationally focused production center specialized in the manufacturing of liquid dosage forms.

Our facility combines cutting-edge GMP-compliant equipment, digital process control, and a high-performing team of experts and leaders.
Rooted in Europe and driven by a global mindset, we develop solutions for international markets – fast, precise, and in full regulatory compliance at the highest level.

Our mission: We empower pharmaceutical companies to bring their products to market safely, efficiently, and on time – as a reliable partner at every stage of the value chain.

Nahaufnahme einer Mitarbeiterin, welche gerade eine Maschine kontrolliert

Open Positions

Would you like to contribute your expertise and commitment to a modern production environment?

Then explore our current vacancies in Production, Quality Assurance, Logistics and Administration. At Lubecafill, you can expect structured processes, long-term development opportunities and a professional team united by common goals.

We welcome unsolicited applications at any time – we look forward to individuals who wish to contribute to our growth with vision and a strong sense of responsibility.

Mitarbeiterin bei der Qualitätssicherung in einer Lohnabfüllung
Head of Quality Assurance (m/f/d)

We are looking for a strong leader to take responsibility for Quality Assurance at our pharmaceutical manufacturing company — someone with strategic foresight and in-depth expertise to continuously advance our GMP system.

  • Establishment, Implementation, and Continuous Development of the Quality Assurance System
    according to GMP, ISO, and other national/international regulatory requirements.
  • Planning, Support, and Follow-up of Regulatory Inspections
    (e.g. TİTCK, FDA, EMA, etc.).
  • Management and Maintenance of All Quality-Related Documentation
    (including SOPs, work instructions, records, etc.).
  • Execution and Follow-up of Change Controls, Deviation Management, and CAPA Processes
  • Planning and Execution of Supplier Audits
  • Quality Assurance Release Processes for Product Launches
  • Development and Implementation of Internal Training Programs
  • Definition and Evaluation of Relevant Quality Metrics (KPIs)
  • Degree in Pharmacy, Chemistry, Biology or a related field of engineering
  • At least 10 years of professional experience in pharmaceutical quality assurance, including ideally 5 years in a managerial role
  • In-depth knowledge of GxP, ISO 9001, and relevant regulatory requirements
  • Proven experience with national and international audits (e.g., TİTCK, EMA)
  • Excellent analytical skills combined with strong planning and organizational competencies
  • Proficient in SAP, OMex, and the Microsoft Office suite
  • Excellent command of English
  • Willingness to work flexible hours
  • Wohnsitz in der Region Çerkezköy / Çorlu
  • Completed military service (for male applicants)
Mitarbeiter beim Qualitätsmanagement in einer Lohnabfüllung
Head of Quality Control Management (m/f/d)

We are looking for a dedicated professional to lead our Quality Control department at our pharmaceutical manufacturing site. This position entails full responsibility for the development, implementation, and continuous optimization of our quality control system in accordance with GMP guidelines.

  • Degree in Chemistry or Chemical Engineering
  • At least 10 years of experience in pharmaceutical quality control laboratories, including a minimum of 5 years in a managerial role
  • Excellent command of English
  • Proficient in using MS Office applications
  • Hands-on experience with SAP and OMex systems
  • For male applicants: completed mandatory military service
  • Willingness to work flexible hours
  • Proven leadership capabilities in guiding and advancing high-performing teams
  • In-depth knowledge of GxP principles and data integrity requirements
  • Experience with TİTCK and EU-GMP inspections, including active participation in regulatory audits
  • Proficiency in operating analytical instruments such as HPLC, GC, UV, IR, AAS, and related technologies
  • Knowledge of documentation practices in quality control laboratories (QCL)
  • Experience with OOS/OOT procedures and the ability to train team members in their implementation
  • Ability to interpret HPLC and GC chromatograms, as well as UV and IR spectra
  • Ensuring and documenting the analysis of intermediates, finished products, raw materials, stability samples, and packaging materials in accordance with SOPs and instructions
  • Experience in cleaning validation processes
  • Involvement in product transfer projects
  • Knowledge in the execution and evaluation of method validations
  • Analytical mindset and solution-oriented working approach
  • Ability to continuously update procedures based on pharmacopoeias, guidelines, and scientific literature

Submit Application

Please use our application form to submit your documents directly to us. The more complete your information, the better we can assess how you might fit in at Lubecafill.

Step

We will get back to you.

After receiving your application, we will contact you personally – by email or phone. In a brief conversation, we will clarify any open questions and discuss which opportunities at Lubecafill may be a good fit for you.

Step

Welcome to Lubecafill

If everything fits, we look forward to welcoming you as a new team member. We place great importance on structured onboarding and a work environment where responsibility and team spirit are valued.

Step

Please make sure that you only upload PDFs with a maximum file size of 2 MB.
You can send us up to 4 files.

Mitarbeiterin stellt Maschine ein
Mitarbeiterin kontrolliert die Abfüllung
Mitarbeiterin bei der Lohnabfüllung