Are you ready to join a

world leader

in the exciting and dynamic fields of the

Pharmaceutical and Medical Device industries? PQE Group

has been at the forefront of these industries

since 1998 , with

40 subsidiaries

and more than

2000 employees in Europe, Asia and the Americas.
We are currently seeking an experienced

Commissioning, Qualification & Validation (CQV) Consultant

in

Barcelona . This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities.
Responsibilities

Execute

commissioning, qualification, and validation activities

for pharmaceutical/biotech equipment and systems
Prepare, review, and execute

C&Q; and validation documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports)
Collaborate with cross‑functional teams

(Engineering, QA, Validation, Manufacturing)

to ensure compliance with

GMP, regulatory guidelines, and project timelines
Review





technical documentation, P&IDs;, FAT/SAT protocols, and vendor manuals
Identify, troubleshoot, and document deviations, ensuring timely resolution
Ensure all activities meet

GMP, FDA, EMA, and ICH requirements
Provide project updates and progress reports to stakeholder
Required Qualifications

Bachelor’s degree in Engineering, Life Sciences, or related field
At least 2 years of experience

in IQ/OQ/PQ protocol development and execution and C&Q; for pharmaceutical/biotech facilities, including construction of production plants
Strong knowledge of GMP, FDA, and EU regulations
Excellent analytical, problem‑solving, and communication skills
Ability to work independently and collaboratively in a project environment.
Spanish native, English fluent (at least B2)
Salary starts from 30.000€ gross per year

📌 CQV Consultant (Madrid)
🏢 Pqe Group
📍 Madrid