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

Ready to take your Quality Control career to the next level in the pharmaceutical industry?

At Remedica, we're looking for a Senior QC Analyst to join our growing Quality Control team in Limassol, Cyprus. This is an excellent opportunity for an experienced laboratory professional to play a key role in ensuring the quality, safety, and compliance of pharmaceutical products supplied to patients around the world. We welcome applications from both local and international candidates and offer a generous relocation package for those moving to Cyprus.

What You'll Be Doing

As a Senior QC Analyst, you'll be responsible for performing and reviewing analytical testing activities across raw materials, in-process materials, finished products, and stability studies. You'll also support investigations, maintain laboratory documentation, and provide technical guidance to junior team members.

Key responsibilities include:

• Performing the necessary tests for raw materials, and the products' intermediate, final and under stability studies, according to written procedures and specifications. Proceeding with the completion of the required documentation.
• Reviewing the documentation and results of the analysis to ensure the validity of the analysis and its conformity with specifications and approve the audit trail.
• Updating laboratory documents (such as reports, methods and analytical protocols) and provide approvals where authorized.
• Ensuring equipment maintenance needs are met, keeping the working area clean and tidy and promptly informing Laboratory Engineers of any equipment troubleshooting needed.
• Reporting updates as regards the status of analysis to QC Supervisors and conduct the relevant investigation when necessary.
• Completing tasks and analysis in accordance with the established regulations and guidelines such as Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), and the current Good Manufacturing Practices (cGMP).
• Carrying out any other duties as assigned by the immediate supervisor.

What We're Looking For

• Bachelor's degree in Chemistry, Chemical Engineering, or a related scientific discipline. Master’s degree in a relevant field will be considered an advantage.
• Previous experience in a pharmaceutical Quality Control laboratory is advantageous.
• Experience with analytical techniques such as HPLC, GC/MS, ICP, TLC, LC/MS, LC/MS/MS, XRD, or PSD would be highly beneficial.
• Strong analytical, problem-solving, and organisational skills.
• Excellent attention to detail and commitment to quality and compliance
• Strong communication skills and the ability to work collaboratively within a team environment.

Ready for Your Next Career Move?

Whether you're already based in Cyprus or considering an international relocation, this is a fantastic opportunity to join a dynamic pharmaceutical environment where your expertise will make a real impact.

Apply today and take the next step in your Quality Control 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.