Manager, Investigations

2 weeks ago


Montréal, Canada Jubilant Pharma Holdings Inc. Full time

English version below

**Rejoignez notre équipe en tant que responsable des enquêtes **

Vous êtes passionné par l'assurance de la qualité et de la conformité dans un environnement pharmaceutique dynamique ? Nous sommes à la recherche d'une personne très motivée pour diriger notre programme de gestion des notifications Jubilant DraxImage et notre système CAPA. En tant que gestionnaire des enquêtes, vous jouerez un rôle crucial dans l'amélioration des processus tout en respectant les normes réglementaires et les objectifs de l'entreprise.

**Pourquoi Jubilant Radiopharma ?**

Chez Jubilant Radiopharma, nous sommes déterminés à avoir un impact significatif sur la vie des patients en fournissant des produits radiopharmaceutiques de haute qualité. En tant que leader de l'industrie, nous offrons des opportunités passionnantes de croissance et de développement professionnels, ainsi qu'un environnement de travail collaboratif où vos contributions sont valorisées et reconnues.

**Principales responsabilités**:

- Mener des enquêtes avec une analyse approfondie des causes profondes et mettre en ?uvre des actions correctives/préventives pour remédier aux écarts de qualité.
- Maintenir la conformité avec les normes et les lignes directrices réglementaires, en veillant à la résolution rapide des problèmes de qualité.
- Suivre les indicateurs de performance clés et fournir des mises à jour périodiques à la direction.
- Recruter et former le personnel, en encourageant une culture de l'excellence et de l'amélioration continue au sein de l'équipe.

**Qualifications**:

- Licence en sciences ou en ingénierie dans un domaine connexe.
- Au moins cinq (5) ans d'expérience dans le soutien aux systèmes de gestion de la qualité des médicaments et/ou des dispositifs médicaux.
- Connaissance approfondie des réglementations et normes BPF (par exemple, FDA 21 CFR 820 / ISO 13485, ISO 14971). Connaissances informatiques (Microsoft Office et environnement SAP).
- Maîtrise du français et de l'anglais, avec de solides compétences interpersonnelles et de communication.

**Rejoignez-nous**:
Si vous êtes à la recherche d'une opportunité à la fois stimulante et gratifiante de faire la différence dans l'industrie de la santé, nous vous invitons à postuler pour notre poste chez Jubilant Radiopharma. Rejoignez-nous dans notre mission de fournir des solutions innovantes qui améliorent les soins aux patients et les conditions de vie. Postulez maintenant et faites partie de notre histoire à succès

**ENGLISH**

**Join Our Team as a Manager of Investigations**

Are you passionate about ensuring quality and compliance within a dynamic pharmaceutical environment? We are seeking a highly motivated individual to lead our Jubilant DraxImage Notification Management program and CAPA system. As the Manager of Investigations, you'll play a crucial role in driving process improvements while adhering to regulatory standards and company objectives.

**Why Jubilant Radiopharma?**

At Jubilant Radiopharma, we are dedicated to making a meaningful impact in the lives of patients by delivering high-quality radiopharmaceuticals. As a leader in the industry, we offer exciting opportunities for professional growth and development, along with a collaborative work environment where your contributions are valued and recognized.

**Key Responsibilities**:

- Lead investigations with thorough root cause analysis and implement corrective/preventive actions to address quality deviations.
- Maintain compliance with regulatory standards and guidelines, ensuring timely resolution of quality issues.
- Track key performance indicators and provide periodic status updates to management.
- Recruit and train staff, fostering a culture of excellence and continuous improvement within the team.

**Qualifications**:

- Bachelor's degree in Science or Engineering in a related field.
- Minimum five (5) years of experience supporting Drug and/or Medical Device Quality Management Systems.
- In-depth knowledge of GMP regulations and standards (e.g., FDA 21 CFR 820 / ISO 13485, ISO 14971).
- Computer literacy (Microsoft Office and SAP environment).
- Bilingual proficiency in French & English, with strong interpersonal and communication skills.

**Join Us**:
Job Overview

**DATE POSTED**:
27/02/24

**LOCATION**:
Montreal, Quebec

**COMPANY**:
Jubilant DraxImage Inc.

**FUNCTION**:
Quality


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