Job Description
Job Title:  Junior CSV Scientist
Job Location (Short):  Cyprus, Limassol
Req ID:  774

Remedica is a leading pharmaceutical company located in Cyprus with pharmaceutical products being distributed in more than 160+ countries worldwide. Originally founded in 1980, it went through various development stages. Today Remedica is specialising in the development, production, and sale of high-quality, safe, and efficacious pharmaceutical products for human use. Our pharmaceutical range consists of a product portfolio of more than 300 generic, branded generic, and over-the-counter (OTC).

Over the last few years, Remedica went through a massive transformational program from a locally recognized 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 Description: 

 

We are looking for:

A Junior Computerized Systems Validation (CSV) Officer to join our team in the pharmaceutical industry. This entry-level role is ideal for someone with a foundational understanding of computerized system validation and a passion for ensuring compliance with regulatory standards.
The Junior CSV Officer will support the validation and maintenance of computerized systems, ensuring they meet GxP and regulatory requirements. 


As a Junior CSV Specialist you will:

  • Assist in the execution of validation activities for computerized systems, including drafting and executing test scripts (IQ/OQ/PQ) 

  • Help develop and maintain validation documentation, such as Validation Plans, Risk Assessments, and Summary Reports.

  • Ensure all validation activities are performed in compliance with regulatory requirements (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5).

  • Support the maintenance and periodic review of validated systems to ensure they remain in a state of control.

  • Assist in troubleshooting system issues and escalating complex problems to senior team members.

  • Ensure all computerized systems comply with GxP, data integrity, and regulatory standards.

  • Support internal and external audits by organizing and providing necessary documentation.

  • Maintain accurate and up-to-date records of validation activities and system changes.

  • Stay informed about industry trends, regulatory updates, and best practices in computerized system validation.

 

What you will bring:

  • Bachelor’s degree in a science discipline, or a related field.

  • At least 2 years of experience in computerized system validation or a related field. Internships or academic projects in CSV or GxP environments are a plus.

  • Basic understanding of GxP regulations, FDA 21 CFR Part 11, EU Annex 11, and GAMP 5 guidelines is preferred.

  • Strong attention to detail and organizational skills.

  • Basic analytical and problem-solving abilities.

  • Good communication and interpersonal skills, with the ability to work effectively in a team.

  • Willingness to learn and adapt to new technologies and processes.

  • Familiarity with quality management systems (QMS) or enterprise resource planning (ERP) systems will be considered a plus

  • Knowledge of data integrity principles and cloud-based systems.

  • Certification or coursework in CSV, GxP, or related areas is a plus.

 

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.
Apply now