Quality Assurance Auditor

BioTalent Canada; Senneville; On-site; CAD 50,000 - 75,000; Full time

Job summary

Join a leading contract research organization as an Auditor in Quality Assurance. You will ensure compliance with regulatory standards by conducting audits, supporting documentation reviews, and communicating findings effectively. This role requires a Bachelor's degree in life sciences and offers a permanent, full-time position with comprehensive benefits.

Benefits

Free shuttle service

Annual bonus based on performance

Competitive benefits including health & dental coverage

Access to on-site gym

3 weeks vacation & 10 personal day policy

Qualifications

• Bachelor’s degree in life science required.
• Knowledge of regulations and guidance.
• Detail-oriented with effective communication skills.

Responsibilities

• Perform audits to ensure compliance with regulations.
• Communicate compliance and quality risks to management.
• Assist in reviewing SOPs and protocols.

Skills

Attention to Detail

Critical Thinking

Communication

Education

Bachelor’s degree in life science

Tools

Microsoft Office

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.

As an Auditor for our Quality Assurance team at the Senneville location, you will perform audits of basic records, reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures.

In this role, primary responsibilities include:

• Communicate all identified compliance and quality risks to supervisor;
• Perform data audits to assess whether records are attributable, legible, contemporaneous, original, accurate, and in compliance with GLP regulations SOPs, and protocols;
• Support the review of SOPs, protocols, and reports to ensure accuracy and compliance with all applicable GLP regulations;
• Prepare written and signed records of all audits and inspections as required. These records may be countersigned by the supervisor or trainer to document the performance of audits and inspections and their reporting to management;
• Assist in the identification of deviations from regulations, protocols, and SOPs.

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

• Bachelor’s degree in life science;
• Knowledge of computer skills including Microsoft Office applications (e.g. Word, Access, Excel);
• Be able to comprehend regulations and guidance documents and apply critical thinking skills to evaluate requirements;
• Be detail oriented and able to effectively communicate findings verbally and in writing.

Role Specific Information:

• 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: Day time from 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.

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 [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.