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Senior Quality Control Analyst & Supervisor

€2,500–3,000 Monthly salary
On-site Work arrangement
Full Time Employment type
Senior-Level Seniority level
Permanent Contract type

Job Description

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.

 

Key responsibilities

  • Lead and supervise the QC laboratory team, ensuring efficient and compliant daily operations.
  • Oversee qualification and requalification of all QC instruments and equipment; review and approve qualification protocols and reports.
  • Manage and approve technical transfers of analytical methods; resolve complex analytical issues and deviations.
  • Review and authorize test results, certificates of analysis (CoA), and batch release documentation.
  • Author, review, and approve SOPs, protocols, and technical reports; ensure documentation complies with GMP and regulatory standards.
  • Coordinate and conduct OOS/OOT investigations; implement and track CAPAs.
  • Act as the QC subject matter expert during internal audits and regulatory inspections.
  • Mentor, train, and develop junior QC Analyst; conduct performance reviews.
  • Collaborate cross-functionally with QA, Regulatory Affairs, and Supply Chain teams.
  • Monitor laboratory KPIs and drive continuous improvement initiatives.

Experience

  • 5+ years in pharmaceutical QC, including supervisory or senior experience
  • Education: Chemistry or related scientific field

 

Skills & competencies

  • Proficiency in English and Greek (written & verbal).
  • In-depth knowledge of GMP, ICH guidelines, and pharmaceutical regulatory requirements.
  • Proven leadership and team management abilities.
  • Strong analytical problem-solving skills, including OOS/deviation management.
  • High attention to detail with a rigorous approach to documentation and data integrity.
  • Effective communication skills with the ability to liaise across departments 
  • Previous experience in participating in GMP audits from the Cyprus pharmaceutical services
How to Apply

To apply, please send your CV to z.mavromoustakis@avvapharma.com

Subject line: "Senior QC Analyst  Supervisor"

Soft Skills
Leadership Team Management Writing reports Critical thinking
Job Categories
Medical Laboratory Technologist
Posted: 16 Jun 2026 Expires: 15 Jul 2026 Ref. No. 6985494

About Company

AVVA PHARMACEUTICALS LTD
AVVA Pharmaceuticals Ltd is a research-based pharmaceutical company, an industry leader in the development and production of innovative medicines that address common medical needs, building on its knowledge derived from the research of the human microbiome.
Limassol, Cyprus Location
11-50 Employees Company size
Pharmaceutical Industry Industry sector
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