CQV & Validation Specialist – Aerospace & Life Sciences

Capgemini; Castelo Branco; Hybrid; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Hybrid work model

Health and life insurance

Referral program with bonuses

Great office locations

Job summary

Capgemini Engineering is seeking professionals with experience in CQV, Validation and/or Process Engineering to join projects in the Aerospace & Life Sciences industries.

Responsibilities include supporting commissioning, qualification, validation and process engineering activities, preparing and maintaining technical documentation, and contributing to CAPA and risk assessment activities.

Qualifications

• 3+ years of professional experience in validation, CQV or process engineering.
• Experience in regulated environments within Aerospace and/or Life Sciences.
• Knowledge of validation methods, documentation and quality systems.
• Experience with IQ/OQ/PQ, risk assessment, CAPA, deviations and change control.

Responsibilities

• Support commissioning, qualification, validation and process engineering activities.
• Prepare, review, execute and maintain validation documentation.
• Create qualification and validation protocols, test cases, reports and evidence.
• Support industrialization, process validation and process optimization.
• Participate in FAT/SAT activities and remote support when required.
• Assist in deviation management, root cause analysis and corrective actions.
• Contribute to CAPA, change control and risk assessment activities.

Skills

CQV

Validation

Process Engineering

Aerospace

Life Sciences

IQ/OQ/PQ

CAPA

Risk Assessment

English

Education

Engineering degree

Technical/Scientific background

Tools

Kneat

Quality management systems

Job description

Capgemini Engineering is seeking professionals with experience in CQV, Validation and/or Process Engineering to join projects in the Aerospace & Life Sciences industries.

Responsibilities include supporting commissioning, qualification, validation and process engineering activities, preparing and maintaining technical documentation, and contributing to CAPA and risk assessment activities.