Research Scientist - Immunology

Microbial Solutions | Charles River; Laval; On-site; CAD 80,000 - 100,000; Full time

Job summary

A leading company is seeking a Research Scientist for their Immunology team in Laval. This role involves designing and conducting laboratory studies, requiring a Master or PhD in Immunology and extensive experience in flow cytometry and immunoassay techniques. The successful candidate will work in a dynamic environment, contributing to significant advancements in drug therapies.

Benefits

Competitive benefits covering up to 85% of health & dental premiums

Free gym on site

Employee and family assistance program

4 weeks’ Vacation & 10 Personal days

Annual bonus based on performance

Qualifications

• 3 to 5 years’ experience working in a Scientific position.
• Experience in development, optimization and use of multi-parameter flow cytometry.
• Experience with immunoassay techniques like ELISAs and cell-based assays is an asset.

Responsibilities

• Design, write, review, and edit study plans and schedules.
• Analyze scientific problems and troubleshoot analytical methods.
• Write scientific documents and review raw data.

Skills

Organizational Skills

Interpersonal Skills

Communication Skills

Problem-Solving Skills

Attention to Detail

Education

Master in Immunology

PhD in Immunology or related discipline

Tools

BD flow cytometer platforms

Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

As a Research Scientist for our Immunology team at the Laval location, you will serve as a Study Scientist or Principal Investigator responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality.

In This Role, Primary Responsibilities Include

• Design, write, review, and edit study plans, amendments and study schedules that define and schedule all study activities;
• Oversee and coordinate all aspects of study related Laboratory Sciences procedures, whether performed within the department or by service departments;
• Analyze scientific problems, troubleshoot analytical methods and technical issues;
• Write scientific documents, review and interpret the raw data;
• Write, review, and edit stand-alone contributing Scientist draft and/or final reports that document all study related procedures and results;
• Prompt verbal or written communications with Study Directors and/or Sponsor on study related business in a timely manner;
• Ensure the accuracy and completeness of project cost estimates;
• Notify the Principal Scientist and/or the Scientific Director of scientist or technical problems as soon as they become apparent.
  
  

Key Elements

We are looking for the following minimum qualifications for this role:

• Holder of a Master in Immunology or any other related discipline with a minimum of 3 to 5 years’ experience working in a Scientific position;
• PhD in Immunology or any biological related discipline;
• 3 to 5 years’ experience in the development, optimization and use of multi-parameter flow cytometry;
• Experience with immunoassay techniques (ELISAs, ECLs, Luminex) and cell-based assays (ELISpot, bioassays) is an asset;
• Experience with the BD flow cytometer platforms; spectral flow cytometry experience is an asset;
• Outstanding organizational skills;
• Good interpersonal and communication skills;
• Strong problem-solving skills;
• Work with precision, pay attention to detail and strive for quality work.
  
  

Role Specific Information

• Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
• Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Monday to Friday, daytime. Depending on the business needs, you may have to do overtime;
• Permanent position as of the hiring, full-time 37.5hrs per week.
  
  

Why Charles River ?

• Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
• Free gym on site;
• Employee and family assistance program;
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
• Access to a doctor and various health professionals (telemedicine);
• 4 weeks’ Vacation & 10 Personal day policy;
• Many social activities!
  
  

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

About Safety AssessmentCharles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles RiverCharles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [e-mail]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

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