[GKE590] - Senior FP&A Analyst

Therapy Management Corporation; Comunidad Valenciana; Presencial; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

An exciting freelance opportunity awaits in Barcelona for a skilled CQV Lead. This role focuses on Commissioning, Qualification, and Validation, particularly in Clean Room Validation Protocol Execution. You will engage in critical CQV activities across various pharmaceutical and biotech projects, ensuring compliance and quality standards are met. This innovative firm is looking for a professional who can travel across Europe and the US, bringing expertise in HVAC and pharmaceutical equipment. If you are ready to take on this challenge and make a significant impact, this is the role for you!

Formación

• Extensive experience in Clean Room Validation Protocol Execution is essential.
• Strong background in pharmaceutical equipment IQ/OQ/PQ is desirable.

Responsabilidades

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

Conocimientos

Clean Room Validation Protocol Execution

HVAC

Travel flexibility

English proficiency

Spanish fluency

Pharmaceutical equipment IQ/OQ/PQ

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 :

1. Clean Room Validation Protocol Execution Experience is a must.
2. HVAC experience is a plus.
3. Must be able to travel across Europe and the US.
4. Proficient in English (mandatory), with Spanish fluency being a strong asset.
5. Experience with other pharmaceutical equipment IQ / OQ / PQ is a great asset.
6. Preference for candidates based in Spain, especially those in or near Barcelona.
7. Freelance (12 months contract).
8. Support critical CQV activities across pharmaceutical and biotech projects.
9. 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. Apply Now or Tag a Colleague at ssanchisoptimussearch.com