Key Skills

Job Description

The Company Our client is a global pharmaceutical company dedicated to improving patients’ lives by developing, manufacturing, and supplying high-quality medicines. With a strong international presence and a broad portfolio of generic and specialty medicines, the organization is committed to making healthcare more accessible and supporting better health outcomes for patients worldwide. Job Description As a QC Analyst, you will perform GMP-regulated analytical testing across in-process controls, raw materials, finished products, and stability samples to ensure product quality and compliance. You will operate laboratory instruments such as HPLC, GC, and UV/VIS, document results, troubleshoot equipment, and support laboratory investigations while working in a rotating 24/5 shift schedule. Responsibilities Perform in-process control testing using techniques such as (U)HPLC, GC, particle size distribution and other chemical methods. Carry out daily environmental monitoring tests, including conductivity, TOC and wet chemical analyses. Complete non-routine testing related to finished product release, stability, raw materials and validation. Evaluate, document and verify analytical results in line with GMP requirements and laboratory procedures. Use laboratory techniques and systems including (U)HPLC, GC, UV/VIS, TOC, particle size analysis and conductivity measurements. Record and manage laboratory data accurately using systems such as LabWare LIMS and Empower. Support laboratory investigations, deviation processes, equipment troubleshooting and analytical problem-solving. Contribute to efficient laboratory operations, reliable sample flow and continuous improvement activities. Requirements MLO or HLO qualification in Analytical Chemistry, Chemistry, Life Sciences or a related field. Experience working in a GMP-regulated laboratory is preferred. Practical experience with HPLC, UPLC, GC or comparable analytical techniques is preferred. Experience with LabWare LIMS, Empower or similar laboratory systems is an advantage. Willingness and ability to work a rotating 24/5 shift schedule. Strong attention to detail and commitment to quality and compliance. A practical, solution-oriented and team-focused approach. Flexibility to work in a changing laboratory and manufacturing environment. Fluent spoken and written English. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

Core Responsibilities

Perform GMP-regulated analytical testing on in-process controls, raw materials, finished products, and stability samples using laboratory instruments and chemical methods. Document and verify results, manage laboratory data, troubleshoot equipment, support investigations, and contribute to efficient laboratory operations and continuous improvement.

Requirements

An MLO or HLO qualification in analytical chemistry, chemistry, life sciences, or a related field is required; experience in a GMP laboratory and practical experience with HPLC, UPLC, GC, or comparable techniques are preferred. Candidates should be fluent in spoken and written English, detail-oriented, quality-focused, solution-oriented, flexible, and willing to work a rotating 24/5 shift schedule; experience with LabWare LIMS, Empower, or similar systems is an advantage.