Remedica is a leading pharmaceutical company located in Cyprus with pharmaceutical products being distributed in more than 140+ countries worldwide. Originally founded in 1980, it went through various development stages. Today Remedica is specialising in the development, production, and sale of high-quality, safe, and efficacious pharmaceutical products for human use. Our pharmaceutical range consists of a product portfolio of more than 300 generic, branded generic, and over-the-counter (OTC).
Over the last few years, Remedica went through a massive transformational program from a locally recognized 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 Quality Systems & Validation – Validation and Qualification Scientist is responsible for supporting and executing qualification and validation activities for facilities, utilities, equipment, computerized systems, processes, and cleaning programs in accordance with current Good Manufacturing Practices (cGMP), regulatory requirements, and company procedures.
The role contributes to the planning, review, execution, and maintenance of qualification and validation programs throughout their lifecycle, ensuring that systems and processes remain in a validated state and are fit for their intended use. Working closely with Engineering, Production, Quality Control, and other stakeholders, the position supports inspection readiness, compliance, and continuous improvement initiatives while ensuring product quality, patient safety, and regulatory compliance.
Duties and Responsibilities:
•Participate in reviewing, approving, setting the requirements and verifying the engineering department and 3rd party vendors for the qualification activities of production equipment, HVAC systems, cleanrooms, utilities (WFI, purified water, compressed air, etc.), and analytical instruments.
•Participate in reviewing, approving, setting the requirements and verifying process validation & cleaning validation activities as per validation master plans and regulatory requirements.
•Support review and approval of validation protocols (IQ, OQ, PQ), reports, risk assessments, and related documentation.
•Verify timely execution of periodic requalification and revalidation as per schedule.
•Support relevant stakeholders with the coordination, planning and execution of validation-related activities
•Ensure compliance with cGMP, FDA, EU, and other global regulatory guidelines relevant to qualification and validation.
•Supporting regulatory inspections, internal audits, and customer audits.
•Support review and approval of Validation Master Plans (VMP), SOPs, and other QA documentation related to validation.
•Investigate & report deviations, change controls, and CAPAs related to validation activities.
•Support technology transfers and new product introductions from a qualification perspective.
•Work closely with cross-functional teams (Production, QC, Engineering)
Qualifications and Experience:
•Bachelor’s Degree in Chemical Engineering, Mechanical Engineering, Chemistry, Biochemistry, Biology or any other related field
•2 years of experience in pharmaceutical QA (qualification/validation) in GMP manufacturing
•Knowledge of GMP, EMA, FDA, WHO, ICH regulations & ISPE guidelines
•Experience in Calibration and Verification of equipment acc. ISO17025
•Good knowledge of the ISO14644 Suite
•Good knowledge of qualification and validation lifecycle and risk-based approaches
•Excellent documentation, review, and audit preparedness skills.
•Analytical thinking and problem-solving skills.
•Strong communication, organisation, and analytical skills.
•Proficient in Microsoft Office (Word, Excel, Outlook).
•Greek & English language: fluent (written and spoken)
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.
