We are looking for:
We are looking for a Cleaning Validation Scientist to be responsible for supporting and executing cleaning validation activities to ensure manufacturing equipment, facilities, and processes are cleaned effectively and consistently in accordance with current Good Manufacturing Practices (cGMP), regulatory requirements, and company procedures.
As a Cleaning Validation Scientist, you will:
1. Cleaning Validation Execution
•Execute cleaning validation studies in accordance with approved protocols and validation plans.
•Support sampling activities, data collection, and documentation during cleaning validation studies.
•Ensure cleaning validation activities are performed in compliance with GMP requirements and internal procedures.
•Contribute to the preparation and review of cleaning validation reports.
2. Cleaning Process Lifecycle Management
•Support maintenance of cleaning processes in a validated state throughout their lifecycle.
•Participate in periodic review, monitoring, and revalidation activities.
•Assist in maintaining scientifically justified cleaning procedures and cleaning limits.
3. Contamination Control & Risk Management
•Support implementation of contamination control strategies related to cleaning processes.
•Participate in risk assessments and cleaning validation evaluations.
•Assist in establishing and maintaining acceptance criteria and cleaning limits.
4. Validation Documentation
•Prepare and review validation documentation, including protocols, reports, risk assessments, and supporting records.
•Ensure documentation complies with GDP and data integrity requirements (ALCOA+).
•Maintain accurate and inspection-ready validation records.
5. Investigations, Deviations & CAPAs
•Participate in investigations related to cleaning failures, deviations, and contamination events.
•Support root cause analysis and implementation of CAPAs.
•Contribute to the assessment of quality events impacting validated cleaning processes.
6. Cross-Functional Collaboration
•Collaborate with Manufacturing, Engineering, Quality Assurance, Quality Control, and other stakeholders.
•Support qualification, technology transfer, and validation projects from a cleaning validation perspective.
•Provide technical input regarding cleaning procedures and validation requirements.
7. Monitoring & Continuous Improvement
•Monitor cleaning validation performance and identify opportunities for improvement.
•Support implementation of improved cleaning technologies and validation approaches.
•Participate in continuous improvement initiatives related to cleaning validation and contamination control.
8. Audits & Readiness
•Support internal audits, customer audits, and regulatory inspections.
•Provide validation documentation and technical support during inspections.
•Ensure ongoing inspection readiness within assigned responsibilities.
9. Compliance & Training
•Maintain knowledge of GMP, validation, and contamination control requirements.
•Participate in training activities related to validation and quality systems.
•Comply with company policies, procedures, and regulatory requirements
What you will bring:
• A bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, Biotechnology, Biology, or a related scientific discipline is required.
•Minimum of 2–4 years of experience in cleaning validation, qualification, manufacturing science, or pharmaceutical quality within a GMP-regulated environment
•Experience supporting cleaning validation activities and contamination control programs is preferred.
•Knowledge of cleaning validation principles and lifecycle management.
•Understanding of contamination control strategies and risk-based validation approaches
•Familiarity with GMP requirements, validation documentation, and quality systems
•Strong analytical, organisational, and problem-solving skills.
•Attention to detail and ability to manage multiple priorities
•Greek: fluent (written and spoken)
•English: fluent (written and spoken)
If you are interested, you can apply via our website: https://careers.remedica.eu/job/Cleaning-Validation-Scientist/1118-en_GB/
Interested candidates are kindly requested to send their CV to the HR Manager at talent@remedica.com.cy.
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.
Join Our Team !
At Remedica, we take pride on our diverse workforce, a global collective of talents representing a multitude of both academic and professional backgrounds. In the tapestry of our organization, our employees are the vibrant threads that bring it to life. Our success is driven by our talented employees that are committed to excellence. For this reason, we are looking to recruit the most talented people from across the world, who bring a diverse range of experience and capabilities to our existing team of experts.
Transparent Communication
We value transparency and effective communication, which is why we regularly host townhall meetings, round tables and open discussions where we share important updates, celebrate our collective successes and provide a platform for open dialogue between leadership and employees.
Cultivating Team Spirit
At Remedica we believe that strong teams drive exceptional results. Our team building events, including parties and social gatherings, offer our people the opportunity to connect on a personal level, strengthen their bonds and build lasting relationships.
Community Engagement
We are also committed to building strong, supporting relationships within our communities. We encourage our people to participate in volunteering opportunities and community service projects, and through several sponsorships and collaborations, we work to enhance public health, promote educational opportunities and support local causes.
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.
