CQV Engineer - Hybrid, Life Sciences Validation Expert

Capgemini Engineering; Fundão; Híbrido; EUR 45 000 - 70 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health and life insurance

Hybrid work

Referral program with bonuses

Great office locations

Resumo da oferta

Capgemini Engineering in Portugal seeks a CQV Engineer to join the Life Sciences team. You will support commissioning and qualification activities in regulated environments, draft and execute validation protocols, and manage documentation across the project lifecycle.

The role requires at least 3 years of CQV/C&Q experience, experience with electronic validation systems (Kneat preferred), and strong collaboration across multidisciplinary teams in an international setting.

Qualificações

• 3+ years in commissioning and qualification (CQV/C&Q) within regulated industries.
• Experience with electronic validation or qualification systems.
• Strong documentation and collaboration across teams.

Responsabilidades

• Support commissioning and qualification activities in regulated environments.
• Draft, review, execute, and maintain CQV lifecycle documentation.
• Prepare and maintain validation protocols, test cases, and system classification documents.
• Execute validation protocols, including prerequisites, testing, and evidence documentation.
• Participate in FAT and SAT activities, including remote support.
• Assist deviation management, test incident resolution, and follow-up actions.
• Contribute to change control activities and ongoing documentation updates.
• Collaborate with multidisciplinary teams and report progress.

Conhecimentos

CQV experience

Validation docs

Regulated environments

Cross-functional teamwork

Formação académica

Pharmacy degree

Biomed/Bioengineering

Ferramentas

Kneat

Quality systems

Descrição da oferta de emprego

Capgemini Engineering in Portugal seeks a CQV Engineer to join the Life Sciences team. You will support commissioning and qualification activities in regulated environments, draft and execute validation protocols, and manage documentation across the project lifecycle.

The role requires at least 3 years of CQV/C&Q experience, experience with electronic validation systems (Kneat preferred), and strong collaboration across multidisciplinary teams in an international setting.