Job Description
Method Validation Chemist
As a Method Validation Chemist, you will be responsible for developing, validating and transferring analytical methods used to support pharmaceutical products and raw materials. Working within a GMP-regulated laboratory, you will play a key role in ensuring analytical methods meet regulatory standards and support quality control and product release.
Key Responsibilities
* Develop and validate analytical methods in accordance with ICH and GMP guidelines
* Perform validation studies including accuracy, precision, specificity, linearity, range and robustness
* Support method transfer between laboratories where required
* Analyse pharmaceutical samples using techniques such as HPLC, GC, UV and dissolution
* Prepare validation protocols, reports and supporting documentation
* Investigate analytical deviations and contribute to continuous improvement activities
* Collaborate with Quality Control, R&D and manufacturing teams to support product lifecycle activities
Requirements
* Degree (or equivalent) in Chemistry, Pharmaceutical Science, or a related scientific discipline
* Experience working in a GMP-regulated pharmaceutical laboratory
* Practical experience in analytical method validation
* Hands-on experience with techniques such as HPLC, GC or other chromatographic methods
* Strong understanding of ICH Q2 and pharmaceutical regulatory expectations
* Excellent attention to detail and strong documentation skills
What’s on Offer
* Competitive salary depending on experience
* Opportunity to join a well-established pharmaceutical organisation
* Supportive and collaborative laboratory environment
* Career development opportunities within a growing company
Apply now or contact CY Partners for more information on this exciting opportunity within the Tyne–Tees pharmaceutical sector.
CY Partners – Talent for Science & Engineering Technologies