The Junior R&D Analyst at Remedica Ltd in Limassol, Cyprus, assists in executing analytical methods, validation studies, and stability tests for new product development under supervision. Responsibilities include operating laboratory instrumentation, documenting analytical results, performing instrument calibration and cleaning, and ensuring compliance with regulatory guidelines. Candidates must hold a degree in Chemistry, Pharmacy, or a related field, with proficiency in English and basic Microsoft Office skills.
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
What’s in it for you?
- 13th and 14th salary.
- Provident Fund.
- Group Medical Plan.
- Discount scheme.
Soft Skills
- Adaptability
If you are interested, you can apply via our website: Junior R&D Analyst Job Details | Remedica Limited
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