IT consultant for pharma and life science

The pharmaceutical industry is subject to strict regulatory requirements from authorities such as EMA, FDA and national medicines agencies. IT systems in the sector must comply with GxP principles (Good Practice) and undergo formal validation processes to ensure data integrity and traceability.

• CSV (Computer System Validation): Formal validation of IT systems supporting regulated processes.
• LIMS and laboratory systems: Laboratory Information Management Systems for sample management and data recording.
• ERP in pharma: SAP and other ERP systems adapted to GxP requirements and batch management.
• Data Integrity: ALCOA+ principles and 21 CFR Part 11 compliance for electronic records.
• MES (Manufacturing Execution Systems): Production control in accordance with GMP requirements.

Pharma companies seek IT consultants who combine technical expertise with knowledge of GxP regulation, validation processes and industry-specific systems.

• CSV specialists: Validation of IT systems in accordance with GAMP 5 and GxP requirements.
• LIMS consultants: Implementation and configuration of laboratory systems.
• SAP pharma specialists: SAP implementation with GxP validation and batch management.
• Data Integrity consultants: Ensuring ALCOA+ compliance and electronic signatures.
• IT project managers with pharma background: Project management with understanding of validation processes and regulatory timelines.

We understand the special requirements that apply in pharmaceutical and life science companies, and we screen consultants for relevant experience with GxP-regulated environments.

• Consultants with documented experience from GxP-regulated companies
• Knowledge of GAMP 5, EMA guidelines and FDA 21 CFR Part 11
• Experience with validation processes and associated documentation (URS, FS, IQ, OQ, PQ)
• Fast matching: screened profiles within 3 working days