Research Scientist - Molecular Biology

Charles River Laboratories, Inc.; Senneville; On-site; CAD 65,000 - 95,000; Full time

Job summary

Join a leading company as a Research Scientist in Molecular Biology, where you will have the opportunity to design and execute studies, develop assays, and analyze data to help advance innovative drug therapies. Bring your expertise in Molecular Biology and contribute to impactful projects within a collaborative team. This full-time position offers comprehensive benefits and is located at our Senneville site, with a daytime schedule from Monday to Friday.

Benefits

Free gym on site

Competitive benefits (health & dental)

Annual bonus based on performance

3 weeks’ vacation and 10 personal days

Employee assistance program

Free shuttle service

Qualifications

• Experience in Molecular Biology is essential.
• Fluency in French and English is preferred.
• Knowledge of GLP is an asset.

Responsibilities

• Design and execute scientific testing strategies.
• Support non-clinical studies related to vector biodistribution.
• Analyze scientific problems and troubleshoot methods.

Skills

Molecular Biology

Communication

Interpersonal Skills

Teamwork

Education

M.Sc. or PhD in Immunology, Microbiology or Virology

Tools

Microsoft Word

Microsoft Excel

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 in Molecular Biology in our immunology team located at the Senneville site, you will be responsible for designing and executing scientific testing strategies and studies, as well as directing assay development, assay validation, or study conduct; examine and interpret study data, communicate results to clients and write final reports.

In this role, primary responsibilities include:

• Support non-clinical studies in assessing vector biodistribution/shedding and/or gene expression as part of safety and/or efficacy assessment;
• Development, optimization and use of qPCR, RT-qPCR, ddPCR, DNA/RNA isolation/quantification assays;
• Write scientific documents, review and interpret the results;
• Analyze scientific problems, troubleshoot analytical methods and technical issues;
• Communicates results to clients and advises clients based on knowledge, experience, best practices and regulatory guidance;
• Management of scientific projects and technical resources involved in study conduct.

Key Elements

We are looking for the following minimum qualifications for this role:
• Molecular Biology experience;
• M.Sc. or PhD in Immunology, microbiology or virology, or in related scientific discipline, or have relevant experience;
• computer literate (Microsoft Word and Excel) and possess excellent communication, interpersonal and teamwork abilities;
• Fluent in French and English. Bilingualism is preferred;
• GLP knowledge (is an asset)

Role Specific Information:
• Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
• Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
• Annual bonus based on performance;
• Schedule: Daytime Monday to Friday;
• 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);
• 3 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 Assessment
Charles 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 River
Charles 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 is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

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, a member of our Human Resources team by sending an ssage to crrecruitment_UScrl. 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, criver.