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Job Title:  Validation Engineer

Job Location (Short):  Cyprus, Limassol

Req ID:  1173

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.

Drive Quality, Compliance & Innovation in Pharmaceutical Manufacturing

At Remedica, quality is at the heart of everything we do. We're looking for a Validation Engineer to play a critical role in ensuring our facilities, systems, equipment, and processes meet the highest regulatory and operational standards.

This is an excellent opportunity for an engineer who enjoys solving complex technical challenges, working across multiple functions, and making a tangible impact on the quality and reliability of pharmaceutical manufacturing operations.

What You'll Be Doing

• Perform commissioning, qualification (IQ/OQ/PQ), and calibration activities
• Execute and document validation lifecycle activities in accordance with approved procedures and validation master plans
• Conduct periodic reviews and requalification activities to ensure continued compliance
• Prepare, review, approve (where authorised) and execute validation protocols, reports, risk assessment, and associated documentation
• Participate in FAT, SAT, commissioning, and qualification activities for new equipment, facilities and systems
• Support change control processes by assessing validation impact and defining required actions
• Investigate deviations, non-conformances, and validation failures, and implement corrective and preventive actions (CAPAs)
• Develop, review, and maintain SOPs, work instructions, and validation documentation
• Support audits and inspections by regulatory authorities, customers, and certification bodies
• Maintain accurate and compliant records within document management systems
• Collaborate with internal departments and external vendors/contractors
• Identify improvement opportunities and implement corrective actions

• Stay up to date with regulatory requirements and industry practices

   

What We're Looking For

• Bachelor's degree in Mechanical, Chemical, Industrial, or a related Engineering discipline.
• Experience within validation, qualification, commissioning, or GMP-regulated environments is an advantage.
• Understanding of GMP requirements and regulatory expectations, including FDA, WHO, ICH, and ISPE guidelines.
• Knowledge of validation lifecycle management and risk-based validation approaches.
• Strong technical writing skills, with the ability to prepare protocols, reports, and compliance documentation.
• Excellent analytical and problem-solving abilities with high attention to detail.
• Strong communication and stakeholder management skills.
• Ability to manage multiple projects and priorities in a fast-paced environment.
• Proficiency in Microsoft Office applications.

What's in it for you?

• Be part of a global pharmaceutical company committed to improving patients' lives through accessible, high-quality medicines.
• Work on major engineering, validation, and facility projects that directly support product quality and regulatory compliance.
• Gain exposure to cutting-edge manufacturing technologies, equipment, and quality systems.
• Collaborate with experienced multidisciplinary teams across Engineering, Quality, Production, and Regulatory Affairs.
• Develop your expertise and build a rewarding career in a growing international pharmaceutical environment.

Ready to help shape the future of pharmaceutical manufacturing? Join us and make your mark as a Validation Engineer at Remedica.

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.

Πώς να υποβάλετε αίτηση

If you are interested, you can apply via our website: https://careers.remedica.eu/job/Validation-Engineer/1173-en_GB

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Remedica Ltd