CHARGE DE PROJET PHARMACEUTIQUE (H/F) - CDI

TN France; Les Ulis; Sur place; EUR 35 000 - 55 000; Plein temps

Résumé du poste

Join a dynamic company in the pharmaceutical industry, where you'll play a crucial role in ensuring the quality of products through rigorous analytical testing. As part of a dedicated team, you'll perform vital analyses, maintain laboratory equipment, and contribute to quality investigations. This position offers a chance to grow your career in a supportive environment focused on innovation and excellence. If you're motivated, curious, and eager to make a difference, this opportunity is perfect for you.

Qualifications

• Experience in a quality control laboratory specialized in physico-chemical analyses.
• Professional English skills preferred for technical communication.

Responsabilités

• Perform analyses for validation of raw materials and finished products.
• Ensure documentation and management of analytical results according to GMP.

Connaissances

Analytical Chemistry

Quality Control

GMP Compliance

Technical Communication

Formation

Bac+2/3 in Analytical Chemistry

Outils

LIMS

Description du poste

Job Details

Client: Eurofins France Pharma

Location:

Job Category: Other

EU work permit required: Yes

Job Reference: 11f06d66e39c

Job Views: 2

Posted: 09.05.2025

Expiry Date: 23.06.2025

Job Description

Directly reporting to the Laboratory Manager «Wet Chemistry», your missions will include:

• Perform analyses for transfer or validation of raw materials and finished products according to analysis methods (Pharmacopoeias or client methods): particle size (laser diffraction, sieves, etc.), physical measurements, limit tests (colorimetric), UV dosage, potentiometric dosage, etc.
• Perform Level I maintenance of laboratory equipment following internal procedures.
• Ensure the maintenance of the responsible area (premises + equipment).
• Verify and correct analytical files.
• Ensure documentation and management of analytical results according to internal procedures and GMP requirements.
• Monitor and coordinate analytical activities of projects (development, validation, and transfer of analytical methods) within the department.
• Communicate with clients regarding technical aspects and project timelines.
• Participate in quality investigations (PACF, OOS) related to analytical problems via LIMS.
• Contribute to laboratory Quality actions (CAPA) based on Quality standards applicable to EPQC.
• Propose and implement actions to improve laboratory efficiency in collaboration with your supervisor.
• Provide technical support to laboratory technicians.
• Provide regular reports to management.

Qualifications

Minimum Bac+2/3 in analytical chemistry with successful experience in a similar role or several years as a technician in a quality control laboratory, specialized in physico-chemical analyses within the pharmaceutical industry under GMP conditions.

Professional English (reading and writing) is preferred.

You are motivated, dynamic, and curious. Autonomous and rigorous, you demonstrate critical thinking and initiative to accomplish your tasks. You enjoy teamwork and idea sharing. Customer satisfaction orientation, adaptability, and flexibility are also important qualities.

If you wish to showcase your skills in a dynamic company offering real career prospects, join us! Please send your application (cover letter + CV + salary expectations) referencing 2025/LU/CP/08 to [emailprotected].