Scientifique / Scientist at Bausch Health Companies
Laval, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

01 Sep, 25

Salary

0.0

Posted On

01 Jun, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Validation, Information Systems, Empower, Metrology, It, Instrumentation, Analytical Techniques, Analytical Chemistry

Industry

Pharmaceuticals

Description

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 itwhere your skills and values drive our collective progress and impact.

DESCRIPTION DE POSTE

Titre du poste : Scientifique (Validation)

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

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
Management information systems: (LIMS, Empower, etc, …)
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.
Bausch Health is an EEO/AA employer M/F/D/V.

Responsibilities

2. MAIN DUTIES

  • 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 (analysis for process validation)
  • 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.

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 residue
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