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