Senior CSV Consultant — Remote (UK) Life Sciences

Rephine; Remote; GBP 100,000 - 125,000; Full time

Job summary

A leading life sciences consultancy is seeking a CSV Consultant (L2) to provide senior-level support in validation and compliance projects remotely from the UK. Ideal candidates have over 5 years of experience, strong knowledge of GMP and GxP regulations, and excellent communication skills. This role offers the chance to work on critical projects, ensuring high-quality consultancy services for pharmaceutical clients while enjoying competitive compensation, flexible hours, and opportunities for growth.

Benefits

Competitive compensation

Work-life balance

Opportunities for growth

Qualifications

• 5+ years in validation and CSV projects in the pharmaceutical or regulated environment.
• Strong understanding of GMP, GxP, and regulatory expectations (EU GMP Annex 11, FDA 21 CFR Part 11, GAMP5).
• Consulting or client-facing experience is a strong plus.

Responsibilities

• Lead and execute CSV and validation activities (planning, risk assessments, IQ / OQ / PQ, reporting).
• Ensure compliance with GMP, GxP, and Data Integrity requirements.
• Act as the main client contact for validation topics.

Skills

Validation and CSV projects

Excellent communication

Proactive mindset

Experience in multidisciplinary teams

Education

University degree in Life Sciences, Engineering, or similar

Tools

ERPs

eDMS

eQMS

LIMS

SCADA

EBRs

Pharmacovigilance systems

Job description

A leading life sciences consultancy is seeking a CSV Consultant (L2) to provide senior-level support in validation and compliance projects remotely from the UK. Ideal candidates have over 5 years of experience, strong knowledge of GMP and GxP regulations, and excellent communication skills. This role offers the chance to work on critical projects, ensuring high-quality consultancy services for pharmaceutical clients while enjoying competitive compensation, flexible hours, and opportunities for growth.