QC Chemistry Laboratory Analyst

Kelix bio (Malta) Ltd

Job Ref: KMP-110726

Kelix bio (Malta) Ltd Logo

Basis

Full-Time

Apply by

22-Nov-2026

Location

Hal Far

Salary

Unspecified

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Kelix Bio Malta is a leading pharmaceutical manufacturing company specialising in sterile injectable finished dosage forms (FDFs) for oncology treatments. As an FDA- and EMA-approved manufacturing facility, we are committed to the highest standards of quality, compliance, and patient safety. Our facility is dedicated to the development and manufacture of liquid and lyophilised sterile pharmaceutical products, serving both local and international markets.

Driven by a passion for excellence, we combine advanced manufacturing capabilities, robust quality systems, and a highly skilled workforce to ensure the reliable supply of high-quality medicines. 

As we continue to grow, we are seeking a dedicated QC Chemistry Laboratory Analyst to join our Quality Control team and contribute to maintaining the highest standards of product quality, patient safety, and regulatory compliance.

Responsibilities

  • To perform chemical testing of raw materials and sterile finished products

  • To perform microbiological water testing and documentation according to the cGLP standards

  • To review documentation before sign-off

  • To ensure compliance with the company’s procedures, policies, local and EU regulations

  • To keep the laboratory documentation in good and accurate condition

  • To perform any other lab-related tasks assigned by the QC Supervisor or QC Manager

  • To perform chemical environmental monitoring of the classified areas according to EU GMP Annex I

  • To perform microbiological method validations

  • To ensure such tasks are completed on time, adequately and efficiently

Requirements

  • A Diploma in Applied Science, or a first Degree in either Chemistry or Laboratory Science 

  • Previous experience within a QC department in a manufacturing pharmaceutical environment

  • Good laboratory practices (cGLP), current Good Manufacturing Practice (cGMP) and other regulatory requirements

  • Ability to communicate in English, both orally and in writing

  • To be able to work alone and as part of a team