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.
We are looking for:
A Junior R&D Analyst for our R&D department. You will familiarize yourself with relevant R&D methods and assist in the execution of assigned Method Development, Method Validation, Process Validation and Stability studies or any other analytical activity needed for the development of new (generic) products or analytical methods. and other important tasks in our R&D center
As a Junior R&D Analyst you will be:
- Learn and execute under supervision any R&D related analytical technique on the instrumentation available (HPLC, dissolution, UV, LC-MS/MS, XRD, PSD, etc.)
- Perform under supervision any analytical task/activities related to the responsibilities of any of the R&D teams (Method Development and Validation, Process Validation and Method transfer, Stability).
- Test materials and products under development
- Proper documentation of the analysis performed, following the respective SOPs
- Review of analytical results and reports (under the supervisor’s guidance)
- Prepare quality reports and other analytical documents
- Follow established procedures that ensure data integrity of the generated results.
- Execute of calibration activities for pH metres and balances
- Execute cleaning activities of instruments used during analysis
- Responsible for the proper application of personal protective equipment and safety procedures
- Ensure that tasks and processes are executed according to established regulations and guidelines such as Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), Good Documentation Practices (cGDP) and the current Good Manufacturing Practices (cGMP).
- Carry out any other duties as assigned by Supervisor/s
What you will bring:
- Degree in Chemistry, Pharmacy or any other relevant field
- HPLC hands on experience is preferred and considered an advantage
- Excellent attention to detail
- Verbal and written communication skills
- Good teamwork skills
- Ability to keep detailed records
- Ability to work under pressure
- Good knowledge of English.
- Basic knowledge of Microsoft office tools
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.
