CQV Lead | Barcelona | Contract / Freelance

Optimus Life Sciences; Comunidad Valenciana; Presencial; EUR 45.000 - 75.000; Jornada completa

Descripción de la vacante

An exciting freelance opportunity has arisen for a skilled CQV Lead in Barcelona, Spain. This role is perfect for professionals with expertise in Commissioning, Qualification, and Validation (CQV), particularly in Clean Room Validation Protocol Execution. You will be engaged in critical activities across pharmaceutical and biotech projects, ensuring compliance and quality standards are met. If you are ready to travel across Europe and the US while making a significant impact in the industry, this could be the ideal position for you. Join a dynamic environment where your skills will be valued and your contributions will drive success.

Formación

• Experience in Clean Room Validation Protocol Execution is essential.
• Proficiency in English and Spanish is preferred.

Responsabilidades

• Support critical CQV activities across pharmaceutical and biotech projects.
• Collaborate on systems qualification and regulatory compliance.

Conocimientos

Clean Room Validation Protocol Execution

HVAC

Travel across Europe and the US

Proficient in English

Spanish fluency

IQ/OQ/PQ experience

Descripción del empleo

Freelance CQV Lead Opportunity in Barcelona, Spain

We're seeking an experienced CQV Lead for a 12-month+ freelance role based in Barcelona, Spain. If you're a highly skilled professional in Commissioning, Qualification, and Validation (CQV) with a strong background in Clean Room Validation Protocol Execution, this could be the perfect opportunity for you!

Key Requirements:

• Clean Room Validation Protocol Execution Experience is a must.
• HVAC experience is a plus.
• Must be able to travel across Europe and the US.
• Proficient in English (mandatory), with Spanish fluency being a strong asset.
• Experience with other pharmaceutical equipment IQ / OQ / PQ is a great asset.
• Preference for candidates based in Spain, especially those in or near Barcelona.
• Freelance (12 months + contract).
• Support critical CQV activities across pharmaceutical and biotech projects.
• Collaborate on systems qualification, documentation, risk assessment, and regulatory compliance.

If you or someone you know fits these criteria, please reach out! Let’s connect and discuss how you can be a part of this exciting role.