Pharma CSV Engineer — Hybrid, Validation Specialist

Tech4Good Recruitment; England; Hybrid; GBP 55,000 - 85,000; Full time

Benefits offered by this job

Hybrid work

Diverse pharma projects

Job summary

Tech4Good Recruitment seeks a dedicated Computer System Validation (CSV) consultant to join pharmaceutical client projects. You will deliver CSV activities, collaborating with quality, engineering and IT teams to ensure systems stay compliant and fit for purpose.

Ideal candidates will have GMP and GAMP knowledge and strong communication skills, with consultancy or client-facing experience and a proven ability to translate regulators into practical validation solutions.

Qualifications

• Strong understanding of GMP regulations and GAMP guidance.
• Excellent communication skills with experience working in a consultancy or client-facing environment.

Responsibilities

• Prepare and execute CSV documentation in accordance with GMP and GAMP guidance.
• Support the validation of new and existing computerised systems within regulated pharmaceutical environments.
• Collaborate with client teams to identify compliance risks and deliver practical validation solutions.

Skills

GMP/GAMP knowledge

Communication skills

Job description

Tech4Good Recruitment seeks a dedicated Computer System Validation (CSV) consultant to join pharmaceutical client projects. You will deliver CSV activities, collaborating with quality, engineering and IT teams to ensure systems stay compliant and fit for purpose.

Ideal candidates will have GMP and GAMP knowledge and strong communication skills, with consultancy or client-facing experience and a proven ability to translate regulators into practical validation solutions.