Scientist in Immunochemistry
- Montreal, QC, Canada
Salary: The hiring range for this position is $61.000 to $78.000/year. · Full-time
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Job details
- Pay
- Salary: The hiring range for this position is $61.000 to $78.000/year.
- Job type
- Full-time
- Apply by
- Experience
- At least 3 years of experience as a Laboratory Analyst;
- Posting language
- English
- Posted
Original job description
Job Overview
As a Scientist for our Immunochemistry team located at the Ville St-Laurent facility, you will be responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.
In This Role, Primary Responsibilities Include
- Write and/or review study schedules, study plans, amendments and standalone and contributing Scientist draft and final reports;
- Prompt verbal or written communication with Sponsors on study related business;
- Oversee and coordinate all aspects of study related procedures, whether performed within the department or by service departments;
- Review and approve raw data;
- Notify the Senior Director, Laboratory Sciences and/or the Associate Scientific Director of technical problems or deviations from budgeted costs as soon as they become apparent;
- Ensures that projects are performed according to Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) regulations and is aware of appropriate regulations, guidelines and guidance.
We are looking for the following minimum qualifications for this role:
- Holder of a Master or a PhD in Biochemistry, Immunology or any other Laboratory Science related discipline;
- At least 3 years of experience as a Laboratory Analyst;
- Outstanding organizational skills;
- Good interpersonal and communication skills;
- Strong problem-solving skills;
- Work with precision, pay attention to detail and strive for quality work.
- Location: 7170 rue Frederick-Banting, Saint-Laurent, QC, H4S 2A1;
- Transportation: Free parking;
- Annual bonus based on performance;
- Schedule: Monday to Friday daytime;
- Permanent position as of the hiring, full-time 37.5hrs per week;
- Salary: The hiring range for this position is $61.000 to $78.000/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications and location.
- We offer competitive benefits and advantages from day one to support your well-being;
- 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!
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, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. 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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More about this job
Responsibilities
Design, conduct, and report Laboratory Sciences studies while ensuring scientific quality, efficient execution, and compliance with SOPs and GLP regulations. Coordinate study procedures, communicate with sponsors, review raw data and reports, and promptly escalate technical issues or budget deviations.
Requirements
A master's or PhD in biochemistry, immunology, or another laboratory science discipline is required, along with at least three years of experience as a Laboratory Analyst. The role also requires strong organizational, interpersonal, communication, and problem-solving skills, as well as precision and attention to detail.
Skills
- Immunochemistry
- Biochemistry
- Immunology
- Laboratory Analysis
- Study Design
- Study Reporting
- Raw Data Review
- Sponsor Communication
- Study Coordination
- Good Laboratory Practice
- Standard Operating Procedures
- Regulatory Compliance
- Organization
- Interpersonal Communication
- Problem-Solving
- Attention To Detail
Benefits
- Performance Bonus
- Free Parking
- Employee And Family Assistance Program
- Telemedicine
- Three Weeks Of Vacation
- Ten Personal Days
- Career Development Opportunities
- Social Activities
- Health And Wellness Coverage
- Stock Purchase Program
- Work-Life Balance Flexibility
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Healthcare
Keywords
- Immunochemistry
- Biochemistry
- Immunology
- Laboratory Sciences
- Laboratory Analyst
- Preclinical Studies
- Study Design
- Study Plans
- Study Schedules
- Study Amendments
- Scientific Reports
- Raw Data
- Sponsor Communication
- Study Coordination
- Standard Operating Procedures
- Good Laboratory Practice
- Regulatory Compliance
- Scientific Quality
- Budget Monitoring
- Safety Assessment
- Drug Development
- Contract Research Organization
- Biotechnology Research