Pharma Equipment Quality & Compliance Lead (IQ/OQ/PQ)

Jce Biotechnology; France; Remote; EUR 55,000 - 75,000; Full time

Job summary

Jce Biotechnology in France is seeking a Quality Officer to drive regulatory compliance and performance of our equipment. You will define customer needs and lead final validation, ensuring adherence to GMP and ISO standards across projects, locally and internationally.

You will build qualification strategies, draft IQ/OQ/PQ protocols and reports, oversee testing, and collaborate with technical teams, production and customers.

Qualifications

• This role requires strong knowledge of ISO standards, GMP and qualification fundamentals.
• Experience in defining customer needs and validation activities is essential.
• Ability to analyze, structure and improve process reliability within a pharmaceutical environment.

Responsibilities

• Define the equipment qualification strategy from customer specifications to final validation.
• Draft IQ/OQ/PQ protocols and reports and oversee testing.
• Ensure strict compliance with pharmaceutical standards and regulatory requirements.
• Collaborate with technical teams, production, after-sales service and customers on-site in France and internationally.
• Travel to customer sites on occasion.

Skills

ISO standards

GMP knowledge

IQ/OQ/PQ fundamentals

Tools

IQ/OQ/PQ protocols

Job description

Jce Biotechnology in France is seeking a Quality Officer to drive regulatory compliance and performance of our equipment. You will define customer needs and lead final validation, ensuring adherence to GMP and ISO standards across projects, locally and internationally.

You will build qualification strategies, draft IQ/OQ/PQ protocols and reports, oversee testing, and collaborate with technical teams, production and customers.