Chargé(e) d'assurance qualité (H/F)

CONSULTYS; Paris; Vor Ort; EUR 45.000 - 60.000; Vollzeit

Benefits dieser Stelle

Mobility support with partial reimbursement of travel expenses

Meal reimbursement

Health coverage with 60% of the premium paid

Comprehensive integration program

Regular training for career development

Zusammenfassung

CONSULTYS, located in Paris, is seeking a Quality Assurance Engineer to support the quality policy and manage compliance in the pharmaceutical sector. Candidates should have 3 to 5 years of experience, preferably with knowledge of BPF and GMP regulations.

The role offers various advantages, including mobility support, meal reimbursement, and health coverage, along with a commitment to career development.

Qualifikationen

• 3 to 5 years of successful experience in Quality Assurance in the pharmaceutical industry.
• Knowledge of relevant references (BPF, GMP).

Aufgaben

• Participate in the diffusion of the quality policy within the company.
• Analyze deviations.
• Participate in investigations.
• Manage change control.
• Implement corrective and preventive actions.
• Serve as quality approver for various documents.

Kenntnisse

Autonomous

Rigorous

Team player

Good organizational abilities

Professional English proficiency

Ausbildung

Engineer or university degree (Bac + 5)

Jobbeschreibung

Job Description

Consultys is a subsidiary of Vulcain Engineering, a consulting and engineering firm specializing in Life Sciences (pharma, biotech, cosmetics, medical devices) in France and internationally. Since 2005, we support industry partners with regional expertise and contribute to sustainable, innovative projects.

Vos Missions

• Participate in the diffusion of the quality policy and culture within the company.
• Analyze deviations.
• Participate in investigations.
• Manage change control.
• Implement corrective and preventive actions.
• Serve as quality approver for various documents (specifications, protocols, reports, traceability matrix, test sheets, test reports, memo).
• Verify compliance with good documentation practices.

Localisation

Région Ile de France.

Required Profile

• Engineer or university degree (Bac + 5).
• 3 to 5 years of successful experience in Quality Assurance in the pharmaceutical industry.
• Knowledge of relevant references (BPF, GMP).

Vos Compétences et Outils

• Autonomous, rigorous, and convincing.
• Team player.
• Good organizational and relational abilities.
• Professional English proficiency.

Vos Avantages

• Mobility support with partial reimbursement of travel expenses.
• Meal reimbursement.
• Health coverage with 60% of the health insurance premium paid.
• Comprehensive integration program and regular training for career development.
• Strong commitment to CSR for a positive, lasting impact.

We are committed to diversity, disability inclusion, and professional equality.