Jobiglo

No results.

GxP Compliance & Computerised System Validation (CSV) Consultant

TRICSOFT TECHNOLOGIES LTD · Kampala

New
Senior 🇬🇧 English
GxP GMP Computerised System Validation CSV Data Integrity GAMP 5 FDA 21 CFR Part 11 EU GMP Annex 11 ERP MES QMS LIMS EDMS

Job description

About the role

An integrated ERP and pharmaceutical operations management platform is being developed for a pharmaceutical manufacturing client. The company is looking for an experienced GxP compliance and computerised system validation (CSV) consultant to bridge the gap between software engineering, pharmaceutical quality systems and validation. The consultant supports the design, review, testing, documentation and validation readiness of the platform, working closely with software engineers, the QA/validation team and process owners.

Key responsibilities

  • Advise on applicable GxP requirements and pharmaceutical computerised system controls
  • Review ERP workflows against pharmaceutical manufacturing and quality processes
  • Support URS, FRS, risk assessments and validation plans
  • Guide IQ, OQ, PQ, UAT and associated validation documentation
  • Advise on data integrity, audit trails, electronic signatures, access controls, segregation of duties and document control
  • Review electronic batch records, traceability, quality management, deviations, CAPA and change control
  • Help set up requirements traceability, test evidence management and validation documentation practices
  • Identify compliance gaps, recommend corrective actions and assess validation readiness
  • Contribute to SOPs, user training and procedures for maintaining the validated state

Required profile

  • Demonstrable experience in pharmaceutical manufacturing, QA, quality systems, regulatory affairs or a related GxP environment
  • Practical understanding of GMP and pharmaceutical quality management
  • Experience or competence in computerised system validation and validation documentation
  • Strong documentation, analytical, communication and stakeholder management skills

Required skills

  • GAMP 5 and risk-based validation (desirable)
  • FDA 21 CFR Part 11 and EU GMP Annex 11 (where applicable)
  • ICH and PIC/S guidance (where applicable)
  • ERP, MES, QMS, LIMS, EDMS or electronic batch record systems (desirable)

This is a project-based consultancy engagement; scope, time commitment, deliverables, duration and fee are agreed with the candidate. Applications with a CV and a brief summary of relevant experience are sent by email by 16 November 2026.

Questions fréquentes

Le salaire n'est pas communiqué publiquement par le recruteur. Vous pouvez postuler et négocier directement avec TRICSOFT TECHNOLOGIES LTD.
Cliquez sur "Postuler maintenant" en haut de la page. Vous pouvez importer votre CV en 1 clic — Jobiglo extrait automatiquement vos informations et postule pour vous.

Why are you reporting this job?

Thank you for your report. We will review this job.

Explore further

Salaries, guides and searches in Uganda.

Apply in 30 seconds

Enter your email to apply. An account will be created automatically.

Apply now →

By continuing, you accept our terms of use.

Already have an account? Login

A question about this job?

Ask it here: you will get the full job summary by e-mail, right away.

Published 4 hours ago

Expires 1 month from now

15 views · 0 interested

Boost your chances

Upload your CV — we will match you with relevant openings.

Analyzing your CV...

TRICSOFT TECHNOLOGIES LTD

Kampala