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.

Location: Limassol, Cyprus (On-Site)

Relocation Support Available

Advance Your Career in Pharmaceutical Quality

Are you an experienced Quality professional looking to make a real impact within a leading international pharmaceutical manufacturer?

At Remedica Ltd, we're seeking a QA Operations Scientist to join our Quality Assurance team in Limassol. This is an exciting opportunity to play a key role in maintaining GMP compliance, supporting operational excellence, and ensuring the highest standards of quality, safety, and efficacy across our pharmaceutical products.

Working at the heart of our manufacturing operations, you'll gain broad exposure to quality systems, investigations, audits, risk management, and continuous improvement initiatives while collaborating with colleagues across the business to drive a culture of quality.

What You'll Be Doing

As a QA Operations Scientist, you'll play a vital role in maintaining and improving our Quality Management System and ensuring operational readiness across the site. Responsibilities include:

• Own GMP documentation, including SOPs, protocols, reports, and quality records.
• Lead investigations into deviations, OOS results, and quality events, driving timely resolution.
• Manage Change Controls and CAPAs, ensuring effective implementation and compliance.
• Support audits, inspections, and site inspection readiness activities.
• Conduct quality risk assessments and identify opportunities to strengthen compliance.
• Investigate customer complaints, temperature excursions, and product quality issues.
• Analyse quality metrics and trends to drive continuous improvement.
• Provide QA support to manufacturing operations through on-floor GMP oversight.
• Contribute to APQRs, quality reviews, and cross-functional quality initiatives.
• Mentor and support colleagues on GMP requirements, quality systems, and best practices.
• Champion a culture of quality, compliance, and operational excellence across the site.

What We're Looking For

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering, or a related scientific discipline.
• 2-3 years' experience within Pharmaceutical Quality Assurance, Quality Control, or GMP Manufacturing.
• Strong understanding of GMP requirements, quality systems, and regulatory compliance.
• Experience investigating deviations, CAPAs, change controls, or related quality processes.
• Excellent analytical and problem-solving skills.
• Strong communication and stakeholder management capabilities.
• High attention to detail and a passion for quality.
• Excellent English language skills; Greek would be advantageous.
• Experience working with electronic Quality Management Systems (eQMS) is beneficial.

This role is based fully on-site in Limassol, Cyprus, and we welcome applications from both local and international candidates. For the right individual, we are happy to provide relocation support to help make the move as seamless as possible.

Ready to Join Us?

If you're passionate about quality, thrive in a GMP-regulated environment, and want to be part of a company that's making a difference in global healthcare, 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.