Pharmaceutical Industry

Cyprus

Remedica Ltd

Biologists

Chemists

Chemical Engineers

We are looking for:A Junior Quality Assurance Scientist to maintain &amp; improve Remedica’s Quality Management System and Operational readiness in order to ensure compliance with GMP regulations concerning quality, safety and efficacy.&nbsp;As a Junior QA Scientist you will:<ul><li>Prepare/issue/review and control of GMP documentation including SOPs, controlled documents, protocols and reports, logbooks. Support document issuance, archiving, and version control.</li><li>Record, track, and perform investigation of deviations and out of specification results.</li><li>Ensure timely initiation and closure of deviation reports.</li><li>Initiate, assess, and track of Change Control records, Ensure risk-based evaluation of changes and appropriate documentation.</li><li>Draft and follow up on Corrective &amp; Preventive actions derived from deviations, audits, complaints, etc. Monitor implementation and verify effectiveness in collaboration with QA team.</li><li>Participate in Interal &amp; External Audits</li><li>Support complaint intake, initial assessment, and coordination of investigations. Participate in the investigation and completion of complaint reports</li><li>Assist in mock recall and documentation of recall procedures.</li><li>Collect and compile data for annual product quality review.</li><li>Assist in evaluation of trends, deviations, OOS, returns, complaints, and CAPAs.</li><li>Participate in Quality Risk Management activities such as risk assessments and mitigation planning.</li><li>Review of qualification/validation protocols and reports (equipment, process, cleaning, transport).</li><li>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.</li><li>Executing onboarding training for new staff and ongoing compliance training activities.</li><li>Maintain training records and ensure training documentation is accurate and up to date.</li><li>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.</li><li>Assist with preparation of quality reports, metrics, and management review data.</li><li>Contribute to the continuous improvement of QMS processes and support inspection readiness.</li></ul>&nbsp;What you will bring:<ul><li>Bachelor’s Degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering or any other related field</li><li>Proficient in English language</li><li>Understanding of GMP (EU, WHO), GDP, and basic pharmaceutical regulations.</li><li>High attention to detail and good documentation practices (GDP).</li><li>Strong communication, organization, and analytical skills.</li><li>Proficient in Microsoft Office (Word, Excel, Outlook).</li><li>Critical Thinking</li><li>Team-oriented, adaptable, and proactive.</li><li>Able to work under fast paced situations</li></ul>If you are interested you can apply via our website:&nbsp;<a target="_blank" rel="noopener noreferrer" href="https://careers.remedica.eu/job/Junior-QA-Scientist/902-en_GB">Junior QA Scientist Job Details | Remedica Limited</a>

Junior Quality Assurance Scientist

Junior Quality Assurance Scientist

RELATED JOBS