Remedica is a globally active EU-based pharmaceutical company, headquartered in Cyprus and present in more than 110 countries. Founded in 1980, the company has evolved into a trusted generics CDMO and dossier development partner for pharmaceutical companies worldwide. Remedica combines development expertise, EU-based manufacturing capabilities, regulatory know-how and a strong quality culture to deliver competitive, high-quality medicines. Its portfolio includes over 300 products across key therapeutic areas, including cardiovascular, oncology, anti-diabetic, anti-infective, central nervous system, alimentary tract, genito-urinary and musculoskeletal treatments.
Over the last few years, Remedica went through a massive transformational program from a locally recognised reputable company to a global player, respected by its distributors, partners, and clients. The investments into the factories, R&D equipment, new facilities, implementation of best-in-class software, and people development are the baselines for Remedica's success in the future.
Job Purpose:
The purpose of this position is to ensure the reliable, compliant, and efficient operation of laboratory equipment across QC, Microbiology, R&D, and other GxP laboratory environments.
The role focuses on maintenance, calibration, qualification, troubleshooting, and continuous improvement of laboratory systems, ensuring that all activities are executed and documented in accordance with engineering standards, regulatory requirements, and company policies.
Duties & Responsibilities:
•Plan, organize, execute, and monitor preventative and corrective maintenance, qualification, and calibration activities for laboratory equipment, ensuring minimal downtime and operational continuity.
•Install, inspect, troubleshoot, repair, and calibrate laboratory equipment.
•Perform routine and preventative maintenance on laboratory systems.
•Qualify new equipment (IQ, OQ, PQ) and maintain the qualified status of existing equipment.
•Schedule maintenance, verification, calibration, and validation activities in a cost-effective and efficient manner.
•Provide technical support to resolve laboratory equipment issues efficiently.
•Ensure accurate and complete documentation of maintenance, qualification, calibration, and troubleshooting activities in compliance with GMP, GLP, and data integrity requirements.
•Maintain and update equipment asset registers and maintenance records in computerized management systems. Coordinate daily laboratory engineering activities, including scheduling, prioritizing service tasks, managing contractors, and liaising with external service providers.
•Source new equipment, spare parts, and external services when required.
•Contribute to the development, review, and continuous improvement of protocols, risk assessments, and Standard Operating Procedures (SOPs).
•Ensure adherence to safety standards, GMP/GLP requirements, and engineering best practices.
•Ensure compliance with data integrity requirements (e.g., FDA 21 CFR Part 11).
•Participate in internal and external audits, providing technical documentation and support.
•Report deviations or non-conformances and assist in implementing corrective actions and CAPAs.
•Participate in cross-functional meetings and continuous improvement initiatives to support laboratory operational excellence.
•Carry out any other duties as assigned by the Engineering Supervisor and/or Engineering Manager.
Qualifications and Skills:
•Bachelor’s degree in Mechanical, Electrical, Chemical Engineering, or related field. Diploma in Electrical/Electronic Engineering or Medical Instruments Technology may also be considered. Master’s degree is an advantage.
•Hands-on experience in laboratory equipment maintenance, engineering support, or technical services. Experience within a GMP or regulated environment is an advantage.
•Strong teamwork and collaboration skills ability to work cross-functionally with QC, Microbiology, QA, R&D, and external vendors.
•Ability to work in laboratory and technical environments, including equipment handling and inspections.
•Good written and verbal communication ability to document technical work and communicate effectively with technical and non-technical stakeholders.
•Good knowledge of Greek and English (written and spoken).
•Basic IT literacy; proficiency in Microsoft Office tools.Experience with maintenance management systems is an advantage.
Salary Range:
Minimum Pay:24,245.00 EUR gross annually
Maximum Pay: 36,367.00 EUR gross annually
Why Join Remedica?
At Remedica, we offer a competitive compensation package, including 14 salaries, a provident fund, and a range of additional benefits to support your personal and professional growth. Join our team and be part of a company that values innovation, teamwork, and continuous improvement.
Equal Opportunity Statement
At Remedica, we are committed to ensuring equal pay for equal work and work of equal value. To support this commitment, roles are evaluated using a structured, gender‑neutral job evaluation framework, which objectively assesses the knowledge, skills, responsibilities, effort, and working conditions associated with each role. This approach helps ensure fair, transparent, and consistent outcomes across the organization.
We welcome applications from all qualified candidates, regardless of sex, race, ethnicity, disability, religion or belief, sexual orientation, gender identity, or age.
