Scientist I

5 days ago

Laval, Canada Nexelis Full time

If you join our team, you will have the chance to participate in the daily life of the most successful advanced testing service provider in the immunology field. Involved in more than 15 SARS-CoV-2 vaccine developments in partnership with multinational pharmaceutical companies, innovative biotechnology companies and prestigious NGOs such as Bill and Melinda Gates Foundation or CEPI, we also proudly serve the needs of our clients in fields such as Flu (universal and seasonal), meningitis, respiratory syncytial virus, chikungunya, malaria, or HPV and are growing an immune-oncology franchise.

If you are interested in working in a dynamic biotechnology environment that is challenging, rewarding and a source of personal pride and growth, we’re interested in hearing from you

Your Main Responsibilities:

- Tabulate and perform final tests review by performing trend analysis, completing all study documentation as required;
- Provide report and/or final results within study timelines and ensure any deviation, exception or events are reflected as appropriate and ensure that all analysis conducted are reported and accurate;
- Assist in writing qualification validation and analytical plans/reports and provide comments and/or recommendations, as needed;
- Assist in the planning of sample analysis by maintaining timeline and scheduling commitments;
- Perform the ordering of reagents, materials and responsible of the inventory for their assigned project(s);
- Write, review and update procedures as needed;
- Support responses to QA reports;
- Provide feedback on progress of work and assist in sponsor teleconferences as required;
- Perform lab activities approximately 50% of the time;
- Conduct all work in compliance with applicable procedures, standards (eg GCLP) and observes all company guidelines and policies;
- Respecting Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures;
- Perform all other tasks as assigned.

What we are looking for:

- Experience in regulated clinical and/or preclinical studies with typically 2 year of experience. Knowledge of regulatory agency guidelines and must understand general procedures and have good knowledge of GCLP regulations;
- Good organizational skill, highly flexible, sense of urgency, excellent troubleshooting skills, client oriented, attentive to details, be able to easily read and understand study plans and protocols, ability to coach/mentor people, good communication skills;
- Knowledge of GDP/GCP/GCLP;
- Understanding of lab operations (LIMS among other things) and ways of working;
- Good in assay troubleshooting;
- Bilingual, both written and spoken in both French and English.

What we can offer:

- Generous time off policy starting at three (3) weeks vacation and five (5) days of sick time
- Employee coverage on medical, dental and vision.
- Employee assistance program.
- Health expense account
- Generous bonus compensation policy

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