A degree in chemistry, chemical engineering, bioengineering, biology or pharmacyAt least 5 years’ professional experience in quality assurance within the pharmaceutical industry, particularly in audit processesGood command of English to participate in meetings with international clients and explain relevant topics during auditsAbility to adapt to a fast-paced working environmentA team-oriented, disciplined, meticulous and dynamic approach to work, as well as strong communication skillsResidence in Çorlu, Çerkezköy, Kapaklı or the surrounding area, or a willingness to live there

Support with the planning, organisation and conduct of regulatory and customer audits through coordinated collaboration with the relevant departments, as well as preparing the plant for auditsSupport in defining corrective and preventive actions following regulatory and customer audits, through coordination with the relevant departments and monitoring of these actions until completionActive involvement in the planning, organisation, reporting and CAPA follow-up of internal audits and supplier auditsSupport in addressing the requirements and quality specifications of national and international customers and regulatory authorities through internal and cross-site coordination and communication with the relevant partiesActive involvement in risk analyses and GAP analyses for all processes at the production plantAssisting with the preparation and finalisation of quality and technical agreements with national and international customers and suppliersOngoing quality assurance work for production materials and other suppliers of materials and services that affect qualityConducting risk assessments on nitrosamines, elemental impurities, and the acceptance of new products and auxiliary raw materialsSupport in the implementation and ongoing development of SOPs and work instructions within the department’s remitSupport with the implementation and ongoing development of SOPs and work instructions within the department’s remit

A degree in engineering, for example industrial engineering, chemical engineering or similar, or in business administration. At least 3 years’ experience in procurement within the pharmaceutical industry. Practical experience in carrying out accounting processes, as well as a thorough understanding of the relevant procedures. Experience in supplier management, price analysis and cost control. Experience in purchasing laboratory consumables and chemicals. Experience in the procurement of machinery, equipment, capital assets, spare parts and maintenance services. Proficiency in using Microsoft Office programmes. The ability to cope with pressure and a willingness to adapt to a fast-paced working environment. The ability to work as part of a team, discipline, attention to detail, dynamism and strong communication skills. A strong sense of responsibility and excellent ability to keep track of tasks. Residence in Çorlu, Çerkezköy, Kapaklı or the surrounding area, or a willingness to relocate there.

Carrying out the company’s procurement activities in accordance with established procedures. Managing suppliers’ tendering processes and carrying out price and cost analyses. Tracking of orders, contracts, deliveries and payment processes. Maintaining supplier relationships and conducting performance reviews. Timely and accurate completion of daily accounting entries. Processing of invoice entries, account reconciliations and bank transactions. Support with monthly closing processes and financial reports. Coordinated collaboration with the relevant departments on tax and regulatory matters. Helping to track stock levels, costs and budgets. Implementation of operational processes in accordance with the legal requirements of the pharmaceutical industry and company procedures.

At least a qualification from a vocational college for industry or a degree from a vocational university in a relevant field. At least two years’ experience in the installation and maintenance of production machinery in the pharmaceutical industry. Excellent communication skills and the ability to work well in a team. Ability to carry out various welding tasks. Ability to read technical documentation for machinery and carry out fault diagnosis. A willingness to engage in continuous learning and personal development. Willingness to work flexible hours and on a shift basis. For male applicants: completion of military service. Residence in Çorlu, Çerkezköy, Kapaklı or the surrounding area, or a willingness to relocate there.

Installation of new production machinery and equipment, as well as active involvement in the commissioning processes. Carrying out regular mechanical maintenance and inspection work in accordance with the schedule. Prompt initial response to any faults that arise and ensuring that they are rectified. Monitoring the work carried out by subcontractors on projects and ensuring compliance with the company’s standards. Carrying out maintenance and repair work in accordance with GMP and health and safety regulations, as well as handling all associated documentation processes.

Career at Lubecafill | Jobs in Pharmaceutical Manufacturing

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.

GMP-Compliance-Specialist

Lubecafill offers state-of-the-art pharmaceutical contract filling services with the aim of redefining quality and efficiency. Our facility in Ergene, Tekirdağ, is being established as an international production centre and focuses on the manufacture of liquid pharmaceutical formulations.

As part of this strong business growth, we are looking for a skilled team member for our Quality Assurance department to fill the role of ‘GMP Compliance Specialist’, who will play an active part in ensuring full compliance with GMP standards and possesses the following qualifications.

General requirements

A degree in chemistry, chemical engineering, bioengineering, biology or pharmacy
At least 5 years’ professional experience in quality assurance within the pharmaceutical industry, particularly in audit processes
Good command of English to participate in meetings with international clients and explain relevant topics during audits
Ability to adapt to a fast-paced working environment
A team-oriented, disciplined, meticulous and dynamic approach to work, as well as strong communication skills
Residence in Çorlu, Çerkezköy, Kapaklı or the surrounding area, or a willingness to live there

Job description

Support with the planning, organisation and conduct of regulatory and customer audits through coordinated collaboration with the relevant departments, as well as preparing the plant for audits
Support in defining corrective and preventive actions following regulatory and customer audits, through coordination with the relevant departments and monitoring of these actions until completion
Active involvement in the planning, organisation, reporting and CAPA follow-up of internal audits and supplier audits
Support in addressing the requirements and quality specifications of national and international customers and regulatory authorities through internal and cross-site coordination and communication with the relevant parties
Active involvement in risk analyses and GAP analyses for all processes at the production plant
Assisting with the preparation and finalisation of quality and technical agreements with national and international customers and suppliers
Ongoing quality assurance work for production materials and other suppliers of materials and services that affect quality
Conducting risk assessments on nitrosamines, elemental impurities, and the acceptance of new products and auxiliary raw materials
Support in the implementation and ongoing development of SOPs and work instructions within the department’s remit
Support with the implementation and ongoing development of SOPs and work instructions within the department’s remit

You can also find further information about the role and the application process on our company profile on Kariyer.net.

Purchasing specialist

Lubecafill offers high-tech pharmaceutical contract filling services with the aim of redefining quality and efficiency. Our facility in Tekirdağ Ergene is being established as an international production centre specialising in the manufacture of liquid pharmaceutical formulations.

As part of this strong organisational structure, we are looking for a capable colleague to fill the role of ‘Purchasing Specialist’, who will work within our Finance Department and play an active part in our purchasing processes. We are seeking a qualified candidate with the qualities listed below.

General requirements

A degree in engineering, for example industrial engineering, chemical engineering or similar, or in business administration.
At least 3 years’ experience in procurement within the pharmaceutical industry.
Practical experience in carrying out accounting processes, as well as a thorough understanding of the relevant procedures.
Experience in supplier management, price analysis and cost control.
Experience in purchasing laboratory consumables and chemicals.
Experience in the procurement of machinery, equipment, capital assets, spare parts and maintenance services.
Proficiency in using Microsoft Office programmes.
The ability to cope with pressure and a willingness to adapt to a fast-paced working environment.
The ability to work as part of a team, discipline, attention to detail, dynamism and strong communication skills.
A strong sense of responsibility and excellent ability to keep track of tasks.
Residence in Çorlu, Çerkezköy, Kapaklı or the surrounding area, or a willingness to relocate there.

Job description

Carrying out the company’s procurement activities in accordance with established procedures.
Managing suppliers’ tendering processes and carrying out price and cost analyses.
Tracking of orders, contracts, deliveries and payment processes.
Maintaining supplier relationships and conducting performance reviews.
Timely and accurate completion of daily accounting entries.
Processing of invoice entries, account reconciliations and bank transactions.
Support with monthly closing processes and financial reports.
Coordinated collaboration with the relevant departments on tax and regulatory matters.
Helping to track stock levels, costs and budgets.
Implementation of operational processes in accordance with the legal requirements of the pharmaceutical industry and company procedures.

You can also find further information about the role and the application process on our company profile on Kariyer.net.

Mechanical Maintenance Technician

Lubecafill offers high-tech pharmaceutical contract filling services with the aim of redefining quality and efficiency. Our facility in Tekirdağ Ergene is being established as an international production centre specialising in the manufacture of liquid pharmaceutical formulations.

As part of this strong organisational structure, we are looking for a competent colleague to fill the role of ‘Mechanical Maintenance Technician’, who will work within our Technical Services department and play an active part in mechanical maintenance processes. We are seeking a qualified candidate with the qualities listed below.

General requirements

At least a qualification from a vocational college for industry or a degree from a vocational university in a relevant field.
At least two years’ experience in the installation and maintenance of production machinery in the pharmaceutical industry.
Excellent communication skills and the ability to work well in a team.
Ability to carry out various welding tasks.
Ability to read technical documentation for machinery and carry out fault diagnosis.
A willingness to engage in continuous learning and personal development.
Willingness to work flexible hours and on a shift basis.
For male applicants: completion of military service.
Residence in Çorlu, Çerkezköy, Kapaklı or the surrounding area, or a willingness to relocate there.

Job description

Installation of new production machinery and equipment, as well as active involvement in the commissioning processes.
Carrying out regular mechanical maintenance and inspection work in accordance with the schedule.
Prompt initial response to any faults that arise and ensuring that they are rectified.
Monitoring the work carried out by subcontractors on projects and ensuring compliance with the company’s standards.
Carrying out maintenance and repair work in accordance with GMP and health and safety regulations, as well as handling all associated documentation processes.

You can also find further information about the role and the application process on our company profile on Kariyer.net.

Contract Manufacturing Organization (CMO)

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GMP-Compliance-Specialist

Purchasing specialist

Mechanical Maintenance Technician

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