Job Description
Pharmaceutical Quality Control Analyst
Location: Oxfordshire
Sector: Pharmaceutical
Our client is a leading Pharmaceutical CRO based in Oxfordshire. Due to continued expansion, they now have an exciting opportunity for an experienced QC Analyst to join the company and support validation studies within the analytical team.
The role:
As a QC Analyst, you will be responsible for analyzing pharmaceutical samples using a range of analytical techniques and supporting various projects. Your main responsibilities will include:
* Validation and verification of analytical methods for HPLC, GC, NMR, KF, etc.
* Conducting degradation and stability studies under different conditions
* Performing LCMS analysis for impurity identification
* Running and reporting on multiple projects simultaneously
* Ensuring all work is performed to the highest quality standards and in compliance with industry guidelines
* Interpreting and reporting laboratory work
Experience expectations:
* Previous pharmaceutical industry experience in an analytical or QC role is essential
* Proficient in analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR
* Knowledge of quantitative and qualitative analysis
* Good understanding of GMP, FDA, and MHRA guidelines
* Experience with method validation and stability studies
* Degree or equivalent in Analytical Chemistry, Pharmaceutical Science, or Chemistry
* Organized and methodical approach to work
* Good communication skills
The package:
Our client offers a permanent position with a competitive salary, benefits, and career progression opportunities. Applicants must be fully eligible to work in the UK. Visa sponsorship is not available for this position, so applicants must not require sponsorship now or in the future.
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