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.

QC Laboratory Analyst

Job Description