Pharmaceutical Industry

Cyprus

AVVA PHARMACEUTICALS LTD

Medical Laboratory Technologist

In addition to performing advanced analytical work, you will oversee day-to-day laboratory operations, mentor junior analysts, and act as a key point of contact for regulatory and cross-functional matters.&nbsp;Key responsibilities<ul><li>Lead and supervise the QC laboratory team, ensuring efficient and compliant daily operations.</li><li>Oversee qualification and requalification of all QC instruments and equipment; review and approve qualification protocols and reports.</li><li>Manage and approve technical transfers of analytical methods; resolve complex analytical issues and deviations.</li><li>Review and authorize test results, certificates of analysis (CoA), and batch release documentation.</li><li>Author, review, and approve SOPs, protocols, and technical reports; ensure documentation complies with GMP and regulatory standards.</li><li>Coordinate and conduct OOS/OOT investigations; implement and track CAPAs.</li><li>Act as the QC subject matter expert during internal audits and regulatory inspections.</li><li>Mentor, train, and develop junior QC Analyst; conduct performance reviews.</li><li>Collaborate cross-functionally with QA, Regulatory Affairs, and Supply Chain teams.</li><li>Monitor laboratory KPIs and drive continuous improvement initiatives.</li></ul>Experience<ul><li>5+ years in pharmaceutical QC, including supervisory or senior experience</li><li>Education: Chemistry or related scientific field</li></ul>&nbsp;Skills &amp; competencies<ul><li>Proficiency in English and Greek (written &amp; verbal).</li><li>In-depth knowledge of GMP, ICH guidelines, and pharmaceutical regulatory requirements.</li><li>Proven leadership and team management abilities.</li><li>Strong analytical problem-solving skills, including OOS/deviation management.</li><li>High attention to detail with a rigorous approach to documentation and data integrity.</li><li>Effective communication skills with the ability to liaise across departments&nbsp;</li><li>Previous experience in participating in GMP audits from the Cyprus pharmaceutical services</li></ul>

Senior Quality Control Analyst & Supervisor

Senior Quality Control Analyst & Supervisor

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