Method Validation Chemist

Position: Method Validation Chemist (Permanent)
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