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

Shape Quality. Drive Compliance. Make a Global Impact.

Are you a quality professional with experience in pharmaceutical manufacturing and a passion for GMP compliance? Do you thrive in regulated environments where attention to detail, continuous improvement, and operational excellence are critical?

At Remedica, we're looking for a Quality Compliance Scientist to join our expanding Quality Assurance team in Limassol, Cyprus. This is an exciting opportunity to play a key role in maintaining inspection readiness, supporting global regulatory compliance, and helping ensure the delivery of high-quality medicines to patients around the world.

For exceptional candidates relocating internationally, we offer a comprehensive relocation package to help make your move to Cyprus as smooth as possible.

What You'll Be Doing

As a Quality Compliance Scientist, you'll work across a broad range of quality and compliance activities, partnering with teams throughout the business to strengthen and maintain our Quality Management System (QMS).

Responsibilities include:

• Act as the primary contact for regulatory authorities pre, during and post Health Authority inspection.
• Ensure compliance with global regulatory requirements ( e.g. EMA, ICH guidelines). Participate and monitor any HA interaction that requires compliance oversight.
• Monitor and interpret new and updated regulations and implement necessary changes
• Prepare/issue/review and control of GMP documentation including SOPs, controlled documents, protocols and reports, logbooks. Support document issuance, archiving, and version control.
• Initiate Change Controls related to regulatory requirement, supplier changes etc. Ensure risk-based evaluation of changes and appropriate documentation.
• Evaluate Corrective & Preventive actions derived from deviations, OOS, complaints, etc. Monitor implementation and verify effectiveness controls.
• Plan, co-ordinate, participate and execute Internal, Supplier and External Audits.
• Manage and ensure timely completion of Corrective & Preventive actions derived from Internal & External Audits.
• Perform onboarding of Suppliers and third-party Services and ensure ongoing compliance and evaluation
• Support customer complaint intake and responses. Participate in the investigation and ensure timely completion of complaint reports.
• Notification and investigation of complaints related to suppliers and third party services.
• Perform recall procedures including mock recall and documentation.
• Evaluation and monitor of Quality Metrics and KPIs.
• Participate in Quality Risk Management activities such as risk assessments and mitigation planning.
• Review of qualification/validation protocols and reports (equipment, process, cleaning, CSV, transport).
• Executing onboarding training for new staff and ongoing compliance training activities.
• Maintain a log of Quality Technical Agreements with suppliers, third-party service providers and partners/customers. Draft, review, and revise quality technical agreements in collaboration with relevant departments.
• Assist with preparation of quality reports, metrics, and management review data.
• Evaluate Allergens, Elemental Impurities, and nitrosamines and other undesirable components for raw materials. Assess risk of components in finished products, prepare, document and share risk assessments outcome and reports.
• Contribute to the continuous improvement of QMS processes and support inspection readiness.
• Ensuring that tasks and processes are executed according to established regulations and guidelines such as Standard Operating Procedures (SOPs), Good Documentation Practices (cGDP) and the current Good Manufacturing Practices (cGMP)
• Carrying out any other duties assigned by the immediate supervisor.

What We're Looking For

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering or another relevant scientific discipline.
• 2-3 years' experience within Pharmaceutical Quality Assurance, Quality Control or GMP Manufacturing.
• Strong understanding of GMP requirements and pharmaceutical regulatory expectations.
• Excellent analytical, investigative and problem-solving skills.
• High attention to detail and commitment to quality.
• Strong communication and stakeholder management skills.
• Excellent English language skills. Greek is an advantage.
• Proficiency with Microsoft Office applications.

This role offers the opportunity to work within an international pharmaceutical organisation where quality and compliance are central to business success. You'll gain exposure to regulatory inspections, supplier quality management, audit programmes, risk assessments and strategic quality initiatives, while working alongside experienced professionals in a collaborative and supportive environment.

Why Limassol?

Combining a rewarding pharmaceutical career with an exceptional Mediterranean lifestyle, Limassol offers year-round sunshine, beautiful beaches, a thriving international community and an outstanding quality of life. Whether you're already in Cyprus or considering an international move, this is a unique opportunity to advance your career in one of Europe's most desirable locations.

Apply Today

If you're ready to take the next step in your Quality career and contribute to the delivery of safe, effective and high-quality medicines 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.