CQV Engineer (Life Sciences)

TL;DR

CQV Engineer (Life Sciences): Support commissioning and qualification activities within regulated environments with an accent on documentation lifecycle and validation protocols. Focus on executing validation protocols using electronic systems (Kneat), managing FAT/SAT activities, and ensuring compliance with SOPs.

Location: Hybrid (Portugal: Fundão, Lisbon, or Vila Nova de Gaia)

Company

Global leader in engineering services providing R&D and digital transformation across multiple industries.

What you will do

• Support commissioning and qualification activities in regulated environments ensuring SOP compliance.
• Draft, review, and maintain C&Q lifecycle documentation using Kneat and other quality systems.
• Prepare and execute validation protocols, test cases, and system classification documents.
• Participate in FAT and SAT activities, providing remote support when required.
• Manage deviations, resolve test incidents, and handle change control activities throughout the project lifecycle.
• Collaborate with multidisciplinary teams and report progress via project trackers.

Requirements

• At least 3 years of experience in commissioning and qualification (CQV or C&Q) within regulated industries.
• Experience working with electronic validation or qualification systems.
• Academic background in Pharmacy, Biomedicine, Biomedical Sciences, or Bioengineering.
• Strong technical documentation skills and high attention to detail.
• Ability to work in a hybrid format from Portugal.

Culture & Benefits

• Hybrid work model and supportive atmosphere promoting work-life balance.
• Health and life insurance.
• Access to career growth programs, training, and certifications in cutting-edge technologies.
• Inclusive, multicultural team environment.
• Referral program with bonuses for talent recommendations.