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.
Quality Control | On-Site | Limassol, Cyprus
Start your career in pharmaceutical quality with one of Cyprus' leading pharmaceutical manufacturers.
At Remedica Ltd, quality is at the heart of everything we do. We are looking for a motivated and detail-oriented Lab Assistant to join our Quality Control team in Limassol, Cyprus. Whether you're looking to begin your career in a laboratory environment or build on existing experience, this is an exciting opportunity to develop your skills within a highly regulated pharmaceutical manufacturing setting.
What You'll Be Doing
As a Lab Assistant, you'll support the daily activities of our Quality Control laboratories, helping to ensure the quality and safety of our pharmaceutical products. Your responsibilities will include:
- Sampling raw materials, intermediates and finished products
- Performing physical quality control tests
- Inspecting products and packaging materials against quality standards
- Handling and monitoring stability samples
- Maintaining accurate laboratory records and documentation
- Supporting analytical testing activities
- Ensuring laboratory equipment and work areas are clean and well maintained
- Working in compliance with SOPs, cGMP and cGLP requirements
What We're Looking For
- Strong attention to detail and a commitment to quality
- Good organisational and analytical skills
- Ability to follow written and verbal instructions accurately
- Strong team-working skills
- Good knowledge of both Greek and English
- Comfortable using basic computer systems and databases
- Previous experience in a laboratory or manufacturing environment is beneficial but not essential
If you're looking for an opportunity to develop your career in Quality Control and gain valuable experience within the pharmaceutical industry, we'd love to hear from you.
Apply today and take the next step in your career with 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.
