Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Technicien(ne) Documentation Qualité GMP / Gestion documentaire (BPF) - Make an Impact at the Forefront of Innovation. This role can be based on site in Montpellier or Sisteron

Operates an archive and document control systems. Logs, stores, retrieves, and monitors circulation of records which may include analytical methods and protocols and project and general laboratory raw data or Investigator site files. Ensures compliance with applicable facility SOP's and FDA Good Pharmaceutical Practices (i.e. Good Laboratory Practices, Good Manufacturing Practices etc) including maintaining security of the archives.

Essential Functions

• Places data and other records in the facility archives and catalogs these items

appropriately to facilitate prompt retrieval. Maintains appropriate tracking

records in the archive database.

• Prepares project and equipment notebooks in accordance with laboratory

specifications. Assigns and distributes notebooks to laboratory staff.

• Catalogues and maintains analytical method and protocol files. Provides

controlled copies of analytical methods to laboratory staff, and maintains

distribution records in the archive database.

• Conducts reviews of study files prior to submission to permanent storage.

• Interacts with commercial (offsite) archive facilities for data storage and

retrieval.

• Troubleshoots and resolves missing or incomplete documentation of the study

boxes.

• May provide training on departmental tasks as appropriate.

Required Qualifications/ Experience:

Education and Experience:

• High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification

• Technical positions may require a certificate

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

• Knowledge of Federal Regulations, ICH GCPs and procedural documents

• Strong computer skills, including MS Office programs

• Strong organizational and time management skills

• Excellent verbal and written communication skills

• Ability to multi-task and handle multiple priorities

• Ability to work in a collaborative team environment

• Fluency in English and French languages

Working Conditions and Environment:

• Work is performed in an office or clinical environment with exposure to electrical office equipment.
• Travel as required by special projects and supervisor needs.
• Long, varied hours required on occasion.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.