We are supporting a pharmaceutical organisation that is continuing to strengthen its Quality Control function and is seeking an experienced Quality Control Analyst to join its GMP laboratory team. This role offers the opportunity to make a meaningful contribution to product quality, compliance and patient safety within a highly regulated environment.
Reporting into senior QC leadership, the Quality Control Analyst will be responsible for routine QC chemistry testing, release activities and support of GMP stability programmes. The position combines hands?on laboratory work with ownership of documentation, data analysis and cross?functional collaboration, making it well suited to a detail?driven QC professional with strong GMP experience.
The role involves execution of analytical and stability testing across raw materials, in?process samples, drug substance and drug product using a range of established techniques. The successful candidate will support stability set?down, pulls, inventory management, sample shipment and receipt, as well as the maintenance, review and trending of stability data. You will also contribute to the creation, review and maintenance of stability protocols, reports and SOPs in line with FDA, EU and ICH requirements.
You will operate within established quality systems, ensuring accurate and compliant documentation and adherence to data integrity standards. The role includes participation in investigations, deviations, change controls and CAPAs, supporting audit readiness and regulatory submissions where required.
This organisation values collaboration, quality and continuous improvement. As such, the role requires a proactive and methodical individual who takes pride in maintaining high standards while contributing positively to a team?focused laboratory environment.
Key Skills & Experience
* BSc (or equivalent) in Chemistry or a related scientific discipline
* 5–7 years’ experience in a pharmaceutical Quality Control laboratory
* hands?on experience with GMP analytical testing, including HPLC/UPLC, GC, UV and related techniques
* experience supporting stability studies from set?down through to reporting
* strong understanding of GMP and GxP requirements
* experience working with LIMS and regulated documentation systems
* high attention to detail with the ability to work both independently and collaboratively
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