QC Laboratory Analyst

We are currently seeking a QC Laboratory Analyst to join a well-established company operating within the pharmaceutical industry.

The successful candidate will work within a GMP-compliant Quality Control laboratory and will be responsible for carrying out analytical testing and supporting the day-to-day activities of the QC department.

Key Responsibilities

• Perform sampling and analytical testing of raw materials, APIs, intermediate products and finished pharmaceutical products.
• Carry out laboratory analysis according to approved methods, specifications and SOPs.
• Perform and document testing using analytical laboratory equipment, including chromatographic techniques such as HPLC and GC, where applicable.
• Compile, review, interpret and accurately document laboratory test results.
• Ensure all laboratory activities are carried out in accordance with GMP/GLP requirements and internal quality procedures.
• Perform routine calibration, verification and maintenance of laboratory equipment.
• Support stability testing and other QC-related analytical activities.
• Prepare and maintain laboratory reagents, standards and solutions.
• Maintain accurate QC documentation, laboratory records, logs and registers.
• Support investigations relating to OOS/OOT results, deviations and other laboratory-related quality issues.
• Ensure proper handling and traceability of samples, standards and laboratory materials.
• Support continuous improvement initiatives within the QC laboratory.
• Work closely with Quality Assurance, Production and other relevant departments when required.

Requirements

• Diploma or Degree in Chemistry, Pharmacy, Pharmaceutical Sciences, Biology, Applied Science or another related scientific discipline.
• Previous experience working within a pharmaceutical QC laboratory is required.
• Good knowledge and practical understanding of GMP principles.
• Previous hands-on experience with analytical techniques such as HPLC, GC, UV spectroscopy or dissolution testing would be highly advantageous.
• Experience with laboratory documentation, SOPs and quality procedures.
• Strong analytical and problem-solving skills.
• Excellent attention to detail and ability to work accurately.
• Good organisational and time-management skills.
• Ability to work both independently and as part of a team.
• Good written and verbal communication skills in English.
• Valid right to work in Malta.

Experience

Ideally 1–3+ years of experience within a pharmaceutical Quality Control laboratory, preferably within pharmaceutical manufacturing, testing or finished-product environments.