Engineer Qualification & Validation/Ingénieur Qualification & Validation

Beckman Coulter Life Sciences; Marseille; Hybride; EUR 40 000 - 60 000; Plein temps

Avantages offerts par ce poste

Hybrid work arrangement

Support for flexible work modalities

Résumé du poste

Beckman Coulter Life Sciences is seeking a Qualification Engineer (f/h) located in Marseille. The role involves qualifying production and laboratory equipment, as well as writing and executing acceptance tests at both supplier and customer sites.

Candidates should possess an academic degree in qualification/validation or a related field, have experience in the pharmaceutical or biotech industries, and be fluent in English and French. The position offers a hybrid work model.

Qualifications

• Academic degree with focus in qualification/validation or a related field.
• First experience in qualification/validation in the pharmaceutical, biotech, chemical or similar industries.
• Fluency in English and French is required.

Responsabilités

• Qualification of production and laboratory equipment.
• Write protocols and perform acceptance tests (FAT/SAT).
• Draft Validation Plan up to Validation reports.

Connaissances

Qualification of production and laboratory equipment

First experience in qualification/validation

Fluency in English and French

Good analytical and synthesis skills

Formation

Academic degree in qualification/validation or related field

Outils

Computerized systems

Description du poste

Job Title: Qualification Engineer (f/h)

Responsibilities

• Qualification of production and laboratory equipment.
• Write protocols and perform acceptance tests at the supplier and at the customer site (FAT/SAT).
• Write and perform Installation, Operational and Performance Qualification (IQ, OQ, PQ) protocols, write the reports and manage associated non‑conformities.
• Draft Validation Plan (VMP) up to Validation reports.

Qualifications

• Academic degree with focus in qualification/validation or a related field.
• First experience in qualification/validation in the pharmaceutical, biotech, chemical or similar industries.
• Fluency in English and French is required.
• Good analytical and synthesis skills, diligence and team spirit.
• Ensure proper application of GMP and GAMP 5 rules.

Additional Experience (Plus)

• Skills in computerized systems, Quality Control department functions and Metrology.

Benefits

• Hybrid work arrangement: part‑time onsite at the specified location and part‑time remote from home.
• Support for flexible and hybrid work modalities for eligible positions.