Quality Lead Technician - Physico chimie - Now Hiring!

Zimmer Biomet; Valence; Sur place; EUR 30 000 - 45 000; Plein temps

Résumé du poste

Zimmer Biomet recherche un Technicien Qualité Lead en physico-chimie à Valence. Le candidat performera des analyses selon les normes GMP et ISO, assurera la conformité des activités de laboratoire et participera à des projets d'amélioration continue. Une connaissance des outils bureautiques et une expérience en physico-chimie sont requises pour ce rôle crucial au sein de l'équipe.

Qualifications

• Compétences techniques en physico-chimie requises.
• Connaissance des normes ISO 13485, ISO 5833 et des BPF.
• Maîtrise des outils bureautiques.

Responsabilités

• Effectuer des analyses dans un laboratoire selon les réglementations applicables.
• Assurer l'exécution correcte de toutes les activités de laboratoire.
• Gérer la documentation et l'équipement du service.

Connaissances

Analyse

Techniques en physico-chimie

BPF (Bonnes Pratiques de Fabrication)

GMP (Good Manufacturing Practices)

Connaissance des normes ISO

Outils

Outils bureautiques

Description du poste

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Quality Lead Technician - Physico chimie - Now Hiring!, Valence

Location: Valence, France

Job Category: Other

EU work permit required: Yes

Job Reference: 413a2c6f968f

Job Views: 3

Posted: 24.06.2025

Expiry Date: 08.08.2025

Job Description:

Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet!

What you can expect

Perform analyses within a laboratory according to applicable regulations (standards, BPF, BPD, HSE, pharmacopoeias), respecting quality policy, instructions, and deadlines.

How you will have an impact

Ensure the proper execution of all laboratory activities in compliance with norms, Good Manufacturing Practices (GMP), Zimmer Biomet directives/procedures, and current procedures.

Manage documentation and equipment of the service.

- Perform analyses prioritizing urgent cases and alert in case of risk of missing deadlines.

- Initiate investigation reports for OOS/OOT results or non-conformities and support their resolution.

- Follow up on CAPA and participate in their implementation.

- Maintain necessary traceability of activities.

- Review and archive analytical records according to your authorizations.

- Send samples and monitor the receipt and review of outsourced analysis results.

- Maintain daily equipment, prepare reagents, and manage stocks.

- Contribute to continuous improvement projects related to laboratory activities.

What sets you apart

Technical skills in physico-chemistry and/or materials are required.

Knowledge of ISO 13485, ISO 5833, and GMP standards.

Proficiency with office tools.

EOE/M/F/Vet/Disability