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.
Job Purpose:
The purpose of this position is to support the planning, coordination, execution, and evaluation of process validation activities in accordance with applicable GMP requirements, regulatory guidelines, and company procedures. The role contributes to ensuring that manufacturing processes remain in a validated state throughout the product lifecycle and supports continuous improvement initiatives to enhance process robustness, product quality, compliance, and operational efficiency. The Process Validation Scientist collaborates with cross-functional teams to generate, analyse, and interpret validation data, prepare validation documentation, and support ongoing process monitoring activities within the manufacturing environment.
Duties & Responsibilities:
- 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.
Qualifications and Skills:
- Bachelor’s degree in Biology, Chemistry, Natural Sciences, Biomedical Sciences, or a related field.
- Master’s degree in a relevant field is considered an advantage.
- Minimum 2-4 years of experience in pharmaceutical, biotechnology, or other regulated manufacturing environments, preparing and executing validation protocols, reports, and technical documentation.
- Ability to collaborate with internal departments, provide guidance, and maintain effective working relationships.
- Positive and proactive approach to problem-solving and teamwork.
- Fluency in English, both written and spoken.
- Additional Greek language proficiency relevant to organization’s operations is considered an advantage.
- Excellent knowledge of Microsoft office tools,
- Experience with statistical and data analysis software (e.g., Minitab, JMP, or equivalent).
- Familiarity with quality management systems, electronic document management systems, and manufacturing-related software platforms.
- Ability to analyze, interpret, and present data using digital tools and reporting systems
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.
