Lighthouse Lab Services is currently seeking a dedicated and detail-oriented R&D; Bioanalytical Scientist / LC-MS Leader to join our client in Laval, QC . This is a full-time position.
Role open to Canadian citizens or permanent residents.
About the Opportunity
Our client is seeking an experienced scientific leader to oversee bioanalytical research and development activities within a GLP-compliant laboratory environment. This role will lead method development using LC-MS, support bioanalysis of small and large molecules, and serve as a key scientific resource across R&D;, laboratory operations, validation, and client-facing activities.
This is an opportunity to lead a growing R&D; function while working with advanced analytical technologies and contributing to the development and evaluation of innovative pharmaceutical products.
Why Live and Work in Quebec?
Quebec offers an exceptional quality of life, combining a vibrant cultural scene with access to beautiful outdoor spaces and a strong life sciences community. With its distinctive French-Canadian culture, excellent food,
and relatively affordable cost of living compared with many major North American cities, Quebec is a unique place to build both a career and a life.
Key Responsibilities
- Lead method development and R&D; activities for bioanalytical assays using LC-MS.
- Provide scientific leadership for bioanalysis of small and large therapeutic molecules.
- Lead, manage, and develop the R&D; team while coordinating departmental activities.
- Serve as the scientific liaison between R&D;, validation, production, and external clients.
- Support recruitment, onboarding, and development of R&D; personnel.
- Serve as a scientific resource for feasibility assessments, project planning, timelines, and technical inquiries.
- Develop new analytical methods and establish verification of client methods according to applicable SOPs.
- Apply robust chemistry expertise to develop and implement current methodologies for creative molecules.
- Review and approve R&D; reports and non-clinical data prior to submission to sponsors.
- Review and approve bioanalytical methods prior to