Ingénieur Qualité F/H (CDI)

JR France; Portet-sur-Garonne; Sur place; EUR 35 000 - 55 000; Plein temps

Résumé du poste

An established industry player in the Healthcare sector is seeking a Quality Engineer to join their dedicated team in the Toulouse region. This role involves collaborating on the Quality Management System, driving continuous improvement initiatives, and managing quality-related projects. The ideal candidate will possess a degree in Engineering or Pharmacy, with a strong background in quality assurance and ISO standards. This position offers a unique opportunity to contribute to a quality culture within a supportive environment, making a significant impact on operational efficiency and product excellence.

Qualifications

• Higher education in Engineering or Pharmacy with a focus on quality.
• Experience in industrial environments handling quality issues.

Responsabilités

• Implement and lead the quality management system according to ISO 9001.
• Lead improvement projects to enhance quality standards.

Connaissances

ISO 9001 Standards

Quality Management Systems

Project Management

Risk Analysis

Continuous Improvement

Analytical Chemistry

Proficiency in English

Formation

Engineering Degree

Pharmacy Degree

Outils

Quality Management Software

Data Analysis Tools

Description du poste

Social network you want to login/join with:

col-narrow-left

Client:

FYTE

Location:

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

664727864301584384032760

Job Views:

2

Posted:

28.04.2025

Expiry Date:

12.06.2025

col-wide

Job Description:

Position: Our client is an international player in the Healthcare Industry.

They are recruiting a Quality Engineer (F/H), on a permanent contract, in Haute-Garonne (Toulouse region).

Within the Purification and Filtration division of the group, on a human-sized site, and in a team of 4 people, your responsibilities include:

1. Participation in the Quality Management System: Collaborate with the Site Quality Manager to implement and lead the quality management system according to ISO 9001 and specific client requirements.
2. Continuous Improvement: Define, formalize, and deploy methods and tools to ensure continuous improvement of products, processes, and the overall system.
3. Project Management: Lead improvement projects to enhance quality standards and operational efficiency.
4. Risk Analysis and Audits: Conduct risk analyses, participate in product decisions, support investigations following anomalies, and participate in external audits.
5. Developing Quality Culture: Promote a quality culture and enhance operational staff's knowledge of standards and client requirements, while acting as backup for the Site Quality Manager in their absence.

Profile: We are looking for a candidate with higher education, such as an Engineer, Pharmacist, or equivalent, with a specialization in quality. Additional training in analytical chemistry is a plus.

Confirmed experience in an industrial environment dealing with quality issues is required. Knowledge of ISO 9001 standards and good practices related to the pharmaceutical industry is appreciated.

Proficiency in English and computer skills are necessary.

Due to the site's location, being vehicle-equipped is essential.

Company: Fyte, part of Morgan Philips Group, specializes in sourcing, evaluating, and recruiting talents for permanent and temporary positions. Our consultants are highly specialized by sector and role, supporting clients through sourcing and selection processes that combine human expertise with the best technology.