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, and 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
Position title: Scientist (Validation)
1. Purpose of the position
- Perform transfers, verifications and validations of both chemical and physical analytical methods for raw materials and finished products.
- Perform optimization of analytical methods and validation work, both chemical and physical, for raw materials, finished products.
- Perform chemical or physical analyzes of raw materials, finished products, and stabilities by known and official methods in order to determine the quality of a product or to follow a manufacturing process.
- Perform analyzes related to laboratory activities in compliance with HSE rules and compliance with GMP, GLP and other guides and standards in force.
- Participate in laboratory activities related to the qualifications of known official methods, manufacturing processes, equipment and washing residues.
- Optimize and validate HPLC and GC analysis methods.
- Participate in the analytical transfer of known and officially approved analytical methods.
- Perform chemical, physical and instrumental analyzes according to known, officially approved methods to determine the quality of products under analysis or to follow a manufacturing process.
- Perform the appropriate follow-up on chemical analyzes.
- Diligently complete the documentation of analyzes carried out according to the standards and procedures in force (BPF, GLP, LIMS, investigations, etc.).
- Participate in the various departmental projects.
- Investigations and re-analyzes following the obtaining of atypical results.
- Qualification and calibration of laboratory instruments.
- Analysis of validation samples of manufacturing processes and stabilities related to projects.
- Participate in various special projects according to the needs of the department.
- Participate in the drafting of procedures and/or operating manual, as needed.
- Is responsible for maintaining his technical qualifications and his knowledge of the methods and procedures in force.
- Calibrate the equipment he uses according to the appropriate programs and for which he has the appropriate knowledge and skills.
- Perform their work in compliance with GMP, GLP and HSE standards, policies and procedures in force in the company.
- Make sure to keep his workstation clean, in accordance with GLP and HSE requirements.
- Ensure the availability of the equipment necessary for the performance of its tasks.
3. Management responsibility
Performs laboratory analyzes (chemical or physical) related to different products and different analytical projects according to known, officially approved methods to determine the quality of the products under analysis or to follow a manufacturing process. Performs analysis method optimization and validation. He is therefore responsible for managing his analysis tasks and their execution and respecting their deadlines.
Act as a resource person during analytical problems on the weights that he or she executes and/or support the use of laboratory instruments, where applicable.
4. Resources (means)
No budget to manage. Expenses to be incurred are the responsibility of the department head.
5. Main professional relationships (internal/external)
Internal partners: The Laboratory department and the purchasing department, in the coordination of their work activities.
External partners: Laboratory analysis service providers.
6. Knowledge and skills required:
a) Required training
Bachelor of Chemistry, Biochemistry.
b) Languages
c) Special experience and knowledge
5 to 7 years of experience in method optimization and validation.
Experience with Empower.
Pharmaceutical analysis laboratory experience.
Knowledge of Canadian and international GMP / GLP standards.
Excellent knowledge of analytical techniques and laboratory instruments (HPLC and GC).
Member of the Ordre des Chimistes.
d) Specific technical skills
Analytical Chemistry.
Instrumentation in the laboratory.
Metrology.
The masculine is used in this publication without prejudice for the sake of conciseness.Bausch Health is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates.
