Method Validation Chemist

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

&#(phone number removed); 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