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.

We are looking for:

A Junior Quality Assurance Scientist to maintain & improve Remedica’s Quality Management System and Operational readiness in order to ensure compliance with GMP regulations concerning quality, safety and efficacy.

 As a Junior QA Scientist you will:

• Prepare/issue/review and control of GMP documentation including SOPs, controlled documents, protocols and reports, logbooks. Support document issuance, archiving, and version control.
• Record, track, and perform investigation of deviations and out of specification results.
• Ensure timely initiation and closure of deviation reports.
• Initiate, assess, and track of Change Control records, Ensure risk-based evaluation of changes and appropriate documentation.
• Draft and follow up on Corrective & Preventive actions derived from deviations, audits, complaints, etc. Monitor implementation and verify effectiveness in collaboration with QA team.
• Participate in Interal & External Audits
• Support complaint intake, initial assessment, and coordination of investigations. Participate in the investigation and completion of complaint reports
• Assist in mock recall and documentation of recall procedures.
• Collect and compile data for annual product quality review.
• Assist in evaluation of trends, deviations, OOS, returns, complaints, and CAPAs.
• Participate in Quality Risk Management activities such as risk assessments and mitigation planning.
• Review of qualification/validation protocols and reports (equipment, process, cleaning, transport).
• Assist in review of manufacturing and packaging batch records. Ensure compliance with BMR/BPR SOPs and GMP requirements. Monitor manufacturing and packaging activities for GMP compliance.
• Executing onboarding training for new staff and ongoing compliance training activities.
• Maintain training records and ensure training documentation is accurate and up to date.
• Maintain a log of Quality Agreements with third-party service providers and partners Assist in the drafting, reviewing, and revision of quality agreements in collaboration with relevant departments.
• Assist with preparation of quality reports, metrics, and management review data.
• Contribute to the continuous improvement of QMS processes and support inspection readiness.

What you will bring:

• Bachelor’s Degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering or any other related field
• Proficient in English language
• Understanding of GMP (EU, WHO), GDP, and basic pharmaceutical regulations.
• High attention to detail and good documentation practices (GDP).
• Strong communication, organization, and analytical skills.
• Proficient in Microsoft Office (Word, Excel, Outlook).
• Critical Thinking
• Team-oriented, adaptable, and proactive.
• Able to work under fast paced situations

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.