Senior Data Integrity Scientist
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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.
Shape the Future of Data Integrity in a GxP Environment
Are you passionate about ensuring data integrity, regulatory compliance, and quality excellence? Do you have the expertise to lead Data Integrity initiatives in a highly regulated pharmaceutical environment?
We are seeking an experienced Senior Data Integrity Scientist to drive and oversee our Data Integrity and Data Governance strategy across GxP-regulated operations. This is a unique opportunity to play a pivotal role in safeguarding data reliability, enhancing compliance, and supporting operational excellence within a dynamic and growing organization.
Why Join Us?
✅ Lead and influence enterprise-wide Data Integrity strategy
✅ Work with cross-functional teams across Quality, Manufacturing, IT, Validation, and Engineering
✅ Play a key role in regulatory inspection readiness and compliance excellence
✅ Shape Data Governance frameworks and best practices
✅ Relocation support available for international candidates moving to Cyprus
As our Senior Data Integrity Scientist, you will be the subject matter expert responsible for ensuring that all GxP data remains accurate, complete, consistent, and compliant throughout its lifecycle in accordance with ALCOA+++ principles.
You will:
- Develop and implement the organization's Data Integrity and Data Governance strategy.
- Lead Data Integrity programs, governance initiatives, and continuous improvement activities.
- Conduct and oversee Data Integrity assessments across manual, hybrid, and electronic systems.
- Drive risk-based remediation plans and ensure sustainable compliance solutions.
- Partner closely with Quality, IT, CSV, and operational teams to embed Data Integrity requirements into systems and processes.
- Support regulatory inspections, audits, and inspection readiness activities.
- Deliver expert guidance, training, and mentoring across the organization.
- Establish metrics, governance forums, and reporting mechanisms to drive continuous improvement.
- Foster a culture of transparency, accountability, and data reliability.
What We're Looking For
- Bachelor's Degree in Pharmacy, Chemistry, Biology, Biotechnology, Engineering, Computer Science, Life Sciences, or a related scientific discipline.
- Minimum 4 years of experience in GxP-regulated industries such as Pharmaceutical, Biotechnology, or Medical Devices.
- Proven experience leading Data Integrity programs and governance initiatives.
- Strong understanding of GMP requirements and Data Integrity regulations.
- Experience participating in regulatory inspections and audits.
- Demonstrated ability to lead cross-functional teams and influence stakeholders at all levels.
- Excellent communication skills in both Greek and English.
You will ideally bring expertise in:
- Data Integrity and Data Governance frameworks
- ALCOA+++ principles
- Computerized System Validation (CSV)
- Quality Risk Management
- CAPAs, Deviations, Change Controls, and Investigations
- Audit Trail Reviews
- Electronic Records and Electronic Signatures
- Data Lifecycle Management
- Regulatory standards including EU GMP, FDA, WHO, MHRA, PIC/S, ICH, and ISPE
- Professional certifications in Data Integrity, Quality Systems, CSV, or GxP Auditing will be considered an advantage.
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.