Validation Lab Technician - GMP/Pharma Impact

Sartorius; Aubagne; Hybride; EUR 32 000 - 46 000; Plein temps

Résumé du poste

Sartorius in Aubagne seeks a Validation Services Laboratory Technician to perform physicochemical tests per validated protocols and prepare records for approval. You will interpret results, maintain data integrity, and support quality/compliance with GMP requirements.

The role requires 3–5 years in a scientific setting, exposure to pharmaceutical contexts, strong communication, and the ability to work in a global environment. Fluency in English is essential.

Qualifications

• Academic or technical degree in sciences / engineering or similar.
• Minimum 3–5 years of work experience, ideally including filtration knowledge.
• Experience in the pharmaceutical industry is a plus.
• Good understanding of GMP requirements.
• Fluent in English.

Responsabilités

• Perform physicochemical tests according to validated protocols.
• Interpret results, complete and review laboratory data, and submit records for final approval.
• Provide qualification/validation quality/compliance support per safety requirements.
• Prepare test solutions and reagents for laboratory tests.
• Handle chemicals and test solutions following regulations and SOPs.
• Inform Laboratory Manager of deviations related to validation protocols or out-of-spec results.
• Perform cleaning and sanitizing of the laboratory and equipment after testing.
• Check monitoring data of laboratory environment and temperature controlled equipment.
• Perform inventory control of consumables and reagents to ensure safety stock.
• Review validation protocols.

Connaissances

Communication

Problem solving

Project management

Teamwork

Self-motivation

Organizational skills

English proficiency

Formation

Science/Engineering degree

Outils

Microsoft Office

Description du poste

Sartorius in Aubagne seeks a Validation Services Laboratory Technician to perform physicochemical tests per validated protocols and prepare records for approval. You will interpret results, maintain data integrity, and support quality/compliance with GMP requirements.

The role requires 3–5 years in a scientific setting, exposure to pharmaceutical contexts, strong communication, and the ability to work in a global environment. Fluency in English is essential.