Validation Analyst

JR United Kingdom; Liverpool City Region; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading company in the pharmaceuticals sector is seeking a Validation Analyst to join their Site Quality function. The role involves ensuring compliance with GMP and GLP, supporting the QC Manager, and utilizing analytical skills for product validation. Candidates should have a degree in Chemical Sciences and extensive experience in pharmaceutical manufacturing.

Qualifications

• 5+ years of experience in pharmaceutical manufacturing and validation.
• Expertise in analytical method validation.

Responsibilities

• Ensure compliance with GMP and GLP in the Quality Control Laboratory.
• Support the QC Manager in testing, validation, and release of products.

Skills

Analytical Skills

Problem-Solving

Communication

Education

Degree in Chemical Sciences

Tools

HPLC

GC

IR Spectroscopy

NIR Spectroscopy

Job description

Validation Analyst – North West England (Pharmaceuticals)

Are you an experienced Validation Analyst with a strong background in pharmaceutical quality control? We’re seeking a dedicated professional to join our Site Quality function and support the QC Manager in ensuring the efficient testing, validation, and release of oral and topical pharmaceutical products.

About the Role

As a Validation Analyst, you’ll play a critical role in the Quality Control Laboratory, ensuring compliance with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP). Your responsibilities will include:

About You

We’re looking for a knowledgeable Validation Analyst with:

• 5+ years of experience in pharmaceutical manufacturing and validation
• Strong analytical skills, with expertise in analytical method validation
• A Degree in Chemical Sciences (or equivalent practical experience)
• Excellent communication, problem-solving, and attention to detail
• Proficiency in HPLC, GC, IR, and NIR spectroscopy