Περιγραφή εργασίας

Job Title:  Process Validation Scientist

Job Location (Short):  Cyprus, Limassol

Req ID:  1174

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.

Help Ensure Every Medicine Meets the Highest Standards

At Remedica, quality isn't just a requirement, it's a commitment. We're looking for a Process Validation Scientist to join our team and play a critical role in ensuring our manufacturing processes consistently deliver safe, effective, and high-quality medicines to patients worldwide.

This is an exciting opportunity to work at the heart of pharmaceutical manufacturing, combining science, data analysis, quality, and continuous improvement to drive process excellence across the product lifecycle.

What You'll Be Doing

• Check the weekly production schedule and determine the need for a process to be validated
• Reviews files, batch manufacturing records and other relevant documentation in order to carry out validation studies and relevant report writing.
• Carry out necessary risk assessment; assist in the response to product/s deficiencies or any other questions arising from external stakeholders, clients and/or authorities in the country or abroad.
• Conducts speed-evaluation tests during compression and physical properties test on materials as and when instructed by the PV Supervisor.
• Update the process validation database through the ERP system
• Provide official reports and evidence that Remedica's products and processes meet the required specified acceptance criteria as those are set by the Authorities.
• Monitor the process under validation during manufacturing and evaluate the data and analytical results.
• Prepare, review and execute process validation protocols and reports.
• Collect, analyze, and interpret process data to assess process capability, consistency, and control, using appropriate statistical and data analysis tools.
• Support investigations related to process deviations, out-of-specification (OOS) results, and atypical events, contributing to root cause analysis and implementation of corrective and preventive actions (CAPAs).
• Ensure compliance with applicable regulatory requirements, including GMP guidelines and internal quality systems.
• Carrying any other duties as assigned by the immediate supervisor.

What We're Looking For

• Bachelor's degree in Biology, Chemistry, Biomedical Sciences, Natural Sciences, or a related scientific discipline.
• 2-4 years of experience in pharmaceutical, biotechnology, or other regulated manufacturing environments.
• Experience preparing and executing validation protocols, reports, and technical documentation.
• Strong analytical mindset with the ability to interpret complex data and identify trends.
• Experience with statistical analysis tools such as Minitab, JMP, or equivalent software.
• Knowledge of GMP requirements, quality management systems, and validation principles.
• Excellent communication skills in English, both written and verbal.
• Greek language skills would be considered an advantage.
• Strong collaboration, problem-solving, and organisational skills.
• Proficiency in Microsoft Office and digital reporting tools.

What's in it for you?

• Contribute directly to the delivery of high-quality medicines that improve patients' lives around the world.
• Work in a highly collaborative environment with exposure to Manufacturing, Quality, R&D, and Regulatory Affairs.
• Develop expertise in process validation, data analysis, quality systems, and pharmaceutical manufacturing.
• Be part of continuous improvement projects that have a real impact on operational performance and product quality.
• Grow your career within a fast-paced, international pharmaceutical organisation committed to innovation and excellence.

Ready to make an impact where science, quality, and manufacturing excellence come together? Apply today and help shape the future of pharmaceutical production at 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.

Πώς να υποβάλετε αίτηση

If you are interested, you can apply via our website: https://careers.remedica.eu/job/Process-Validation-Scientist/1174-en_GB

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Remedica Ltd