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.

Limassol, Cyprus | On-Site

Relocation Package Available

Are you a scientifically minded professional with a passion for analytical testing and quality? Looking for an opportunity to develop your career within a growing international pharmaceutical organisation?

At Remedica Ltd, we're seeking a QC Analyst to join our Quality Control team in Limassol, Cyprus. In this role, you'll play a vital part in ensuring that raw materials, in-process materials, finished products, and stability samples meet the highest quality and regulatory standards before reaching patients around the world.

Working within a GMP-regulated laboratory environment, you'll have the opportunity to perform a broad range of analytical testing, collaborate with experienced scientists, and contribute to the continuous improvement of laboratory processes and analytical methods

What You'll Do

• Perform testing of raw materials, in-process products, finished products, and stability samples.
• Review and verify analytical results and laboratory documentation.
• Prepare reports, analytical protocols, and quality records.
• Support the evaluation and implementation of analytical methods and procedures.
• Monitoring equipment maintenance needs, keeping the working area clean and tidy and promptly informing Laboratory Engineers of any equipment troubleshooting needed.
• Investigate laboratory issues and communicate findings to key stakeholders.
• Maintain compliance with cGMP, cGLP, SOPs, and regulatory requirements.
• Contribute to continuous improvement initiatives across the laboratory.

What We're Looking For

• Bachelor's degree in Chemistry, Pharmacy, Chemical Engineering, or another relevant scientific discipline.  A Master’s degree in a relevant field would be considered an advantage.
• Previous pharmaceutical laboratory experience as a Junior QC Analyst or equivalent role.
• Experience with analytical techniques such as HPLC, GC/MS, LC/MS, ICP, TLC, XRD, or similar would be beneficial.
• Strong analytical and problem-solving skills.
• Excellent attention to detail and commitment to accuracy.
• Strong communication and collaboration skills.
• Good command of English. Greek language skills are a nice to have but not essential.

This role is based fully on-site in Limassol, Cyprus. We welcome applications from both local and international candidates, and relocation support is available for the right candidate.

Apply Today

If you're looking for a role where your scientific expertise will directly contribute to delivering high-quality medicines to patients worldwide, we'd love to hear from you.

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.