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 recent graduate in a scientific discipline looking to launch your career in the pharmaceutical industry?

At Remedica, we are passionate about improving lives through the development and manufacture of high-quality medicines supplied to patients around the world. We are seeking a Junior QA Operations Scientist to join our growing Quality Assurance team in Limassol, Cyprus.

This is an excellent opportunity for an ambitious graduate or early-career professional to gain hands-on experience within a highly regulated pharmaceutical manufacturing environment, working alongside experienced quality professionals and playing a key role in maintaining compliance, product quality, and patient safety.

Why Join Remedica?

• Join one of Cyprus' leading pharmaceutical manufacturers
• Build your career within a global, GMP-regulated environment
• Gain exposure to Quality Management Systems, investigations, CAPAs, audits, and regulatory compliance
• Work with experienced professionals across Quality, Production, Laboratories, and Supply Chain
• Competitive compensation and benefits package
• Comprehensive relocation support for international candidates
• Opportunity for professional growth and long-term career development

What You'll Be Doing

As a Junior QA Operations Scientist, you will support the maintenance and continuous improvement of our Quality Management System while helping to ensure compliance with GMP requirements.

Key responsibilities include:

• Supporting GMP documentation activities, including SOPs, protocols, reports, and controlled documents
• Assisting with deviation, complaint, and OOS investigations
• Managing and tracking Change Controls and CAPAs
• Supporting audit preparation and inspection readiness activities
• Participating in Product Quality Reviews and quality metrics reporting
• Contributing to Quality Risk Management activities
• Supporting GMP oversight within manufacturing and packaging operations
• Working collaboratively with cross-functional teams to drive quality excellence
• Contributing to continuous improvement initiatives across the Quality function

What We're Looking For

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering, or a related scientific field
• Recent graduates are encouraged to apply; no prior industry experience is required
• Strong attention to detail and analytical thinking skills
• Excellent written and verbal communication skills
• Ability to thrive in a collaborative, fast-paced environment
• Strong Microsoft Office skills
• Excellent English language skills
• Experience with electronic Quality Management Systems (eQMS) would be an advantage

Location & Relocation

This position is fully on-site in Limassol, Cyprus.

We welcome applications from candidates located both within Cyprus and internationally. For candidates relocating from abroad, Remedica offers a comprehensive relocation package and support to help ensure a smooth transition.

Apply Today

If you are looking to start your career in Quality Assurance within a dynamic pharmaceutical manufacturing environment and want to be part of a company committed to quality, innovation, and patient wellbeing, 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.