Team Leader Quality

Join a team We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufacture and market a range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Our 7,000 employees share a common goal and values, propelling us to provide essential care to millions of people globally. We seek dedicated individuals who share our sense of urgency, unity, and excellence.

We are looking for a trustworthy and respectful individual who consistently does the right thing. Someone who is imaginative and proactive, with a keen eye for what is possible. A perceptive and adaptive person who is action oriented. We need a disciplined, focused, and accountable team member. If you embody these values, come join our company and help us shape the future.

We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.

**Job Description**:

- Ensures the coordination of compliance activities such as Supplier management, Licensing Quality Agreements, Internal audit and Investigations
- Ensures coordination of activities internally related to these compliance systems and ensures the KPIs are tracked and communicated
- Responsible for supervision of the compliance specialists responsible for the tasks related to the Compliance activities
- Supplier Management
- Ensures that supplier program is up to date
- Ensure external audits are performed
- In conjunction with Procurement, performs supplier reviews and coordinates supplier issues and communications

Quality Agreements
- Manages quality agreement updates within timelines required by the procedure
- Coordinates new quality agreements issuance

Investigations
- Provides quality support for investigations and participates in SWOT team activities for site investigaitons
- Manages the investigations system including ensuring the investigations are completed on time and as per requirements
- Provides KPIs for investigations

Internal Audit
- Responsible for the internal audit program
- Provides KPIs for investigations

Licenses
- Responsible for filing of the DELs, Table A and other site licenses

Management Responsibilities
- Veille à entretenir un climat propice à une bonne performance des équipes.
- Relaie les informations entre sa hiérarchie et l’équipe.
- Participe à l’évaluation de ses collaborateurs et participe à leur développement notamment par l’identification des besoins de formation.
- Effectue le suivi des vacances en fonction des besoins de la cédule.

Skills and Qualifications
- Training required
- BSc in science or equivalent combination of experience and academic education Languages - French and English
- Special knowledge and experience
- Minimum 5 years’ experience in a pharmaceutical industry
- Experience required in GMP, Quality systems, investigation writing and audit
- GMP knowledge
- Knowledge of investigation writing tools (5whys/ ishikawa)
- Knowledge of production flows/steps
- Knowledge of use of Microsoft office tools

**This position may be available in the following location(s)**:Laval, QC**

Any exception will have to be authorized by your HR Business Partner.

Bausch Health Companies Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Job Applicants should be aware of job offer scams perpetrated through the Internet and social media platforms.

Bausch Health is an EEO/AA employer M/F/D/V.