GxP QA Lead — GMP/GLP Compliance & Audits

MedPharm Ltd; Guildford; On-site; GBP 40,000 - 60,000; Full time

Job summary

A pharmaceutical company in Guildford is seeking a QA Specialist to ensure compliance with GLP, GMP, and MHRA regulations. The role demands oversight of QA activities, batch release processes, and regulatory audits. Candidates should possess a Bachelor’s degree and 3+ years of experience in a GMP environment. Strong knowledge of GMP standards and excellent communication skills are essential. This is a full-time on-site position with occasional travel for training or audits.

Qualifications

• Minimum 3 years of experience in a GMP-regulated QA environment.
• Experience in GMP manufacturing, batch release, and QMS management is essential.

Responsibilities

• Oversee day-to-day QA activities associated with IMP manufacturing.
• Provide quality oversight for batch record review and line clearances.
• Lead internal audits and support external audits for compliance.

Skills

In-depth knowledge of GMP

Strong understanding of IMP requirements

Excellent written and verbal communication skills

Highly organized with strong attention to detail

Proficiency with Microsoft Office

Education

Bachelor's degree in scientific or related discipline

Tools

Electronic QMS

Job description

A pharmaceutical company in Guildford is seeking a QA Specialist to ensure compliance with GLP, GMP, and MHRA regulations. The role demands oversight of QA activities, batch release processes, and regulatory audits. Candidates should possess a Bachelor’s degree and 3+ years of experience in a GMP environment. Strong knowledge of GMP standards and excellent communication skills are essential. This is a full-time on-site position with occasional travel for training or audits.