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A career as a Senior Indirect Tax Compliance Analyst in National Bank's Finance sector means acting as a professional reference in the team, participating in the definition of strategic orientations and policies related to your field, as well as contributing to the maintenance of partnerships with various internal and external stakeholders within the framework of joint projects. It is thanks to your solid experience in accounting and particularly your knowledge of indirect taxes that you will lead large-scale projects that require a high level of experience and expertise. Your job Ensure commodity tax compliance (GST-HST-QST-PST) for various entities within the NBC Group Carry out the control and analysis of various accounting or financial transactions to ensure their compliance with the legislation in force Support our various partners in the Finance and business sectors in decision-making Actively participate in accounting and government audits Adapt work tools and analyses according to the needs and new activities of the sector Ensure the development, implementation, monitoring and control of systems, tools and work processes and formulate recommendations in order to optimize the efficiency of operations and the quality of financial informationYour job Your team Within the Finance sector, you will be part of a team of 4 colleagues and will report to the Director, Commodity Tax Compliance. The team is responsible for accounting, controlling and reporting commodity taxes as well as government audits. This position will allow you to develop in the field of indirect taxes for financial institutions. In particular, you will have the opportunity to gain knowledge about the activities of the bank and its subsidiaries. You will join a dynamic team in which everyone collaborates to achieve a common goal. Prerequisite Bachelor's degree in accounting completed and 6 years of relevant experience OR Master's degree in accounting and 4 years of relevant experience Advanced knowledge with Excel Ability to work with multiple systems and subsystems to extract information needed for accounting analysis Excellent interpersonal skills Respect for deadlines, rigor, meticulousness Strong team player Developed sense of autonomy and organization Have a strong ability to adapt to changes#LI-SR1 Your benefitsIn addition to competitive compensation, upon hiring you’ll be eligible for a wide range of flexible benefits to help promote your wellbeing and that of your family.Health and wellness program, including many optionsFlexible group insuranceGenerous pension planEmployee Share Ownership PlanEmployee and Family Assistance ProgramPreferential banking servicesOpportunities to get involved in community initiativesTelemedicine serviceVirtual sleep clinicThese are a few of the benefits available to you. We have an offer that keeps up with trends as well as your needs and those of your family. Our dynamic work environments and cutting-edge collaboration tools foster a positive employee experience. We actively listen to employees’ ideas. Whether through our surveys or programs, regular feedback and ongoing communication is encouraged.We're putting people firstWe're a bank on a human scale that stands out for its courage, entrepreneurial culture, and passion for people. Our mission is to have a positive impact on peoples' lives. Our core values of partnership, agility, and empowerment inspire us, and inclusivity is central to our commitments. We offer a barrier-free workplace that is accessible to all employees. We want our recruitment process to be fully accessible. If you require accommodation, feel free to let us know during your first conversations with us. We welcome all candidates! What can you bring to our team?Come live your ambitions with us!

Director Financial Crime Apply now » Apply now Start applying with LinkedIn Apply Now Start Please wait... Apply now × Apply for Job × × × Enter your email to apply Date: May 13, 2024 Location: Montreal, Quebec, Canada Company: Deloitte Job Type: Permanent Work Model: Hybrid Reference code: 126372 Primary Location: Montreal, QC All Available Locations: Montreal, QC Our Purpose At Deloitte, we are driven to inspire and help our people, organization, communities, and country to thrive. Our Purpose is to build a better future by accelerating and expanding access to knowledge. Purpose defines who we are and gives us reason to exist as an organization. By living our Purpose, we will make an impact that matters Have many careers in one Firm. Partner with clients to solve their most complex problems Enjoy flexible, proactive, and practical benefits that foster a culture of well-being and connectedness. Experience a firm where wellness matters. -- What will your typical day look like? Lead diverse teams of talented advisors on key client projects Execute a client service plan on complex engagements and work closely with the Partners to exceed our client's expectations while identifying and mitigating business risks associated with projects Cultivate long term relationships with clients and key contacts/influencers Possess strong knowledge of leveraging prevalent methodologies Direct a structured approach to project management to ensure complete client satisfaction and project profitability Develop your expertise in a specialization and enhance your reputation as a business advisor, becoming a thought-leader in your area of specialization Contribute significantly to practice growth and development, supporting Partners Participate in the development and delivery of training programs Coach and mentor select practitioners to their highest potential and be a role model Create a learning environment through leadership About the team Deloitte's team of Forensic professionals advises clients and their counsel by identifying, investigating and resolving financial crimes and other behaviors resulting in financial, reputational and/or regulatory risk. They help major corporations, institutions, governments and regulators in Canada and worldwide to mitigate the risk of financial crime, including money laundering, fraud, and corruption. The Forensic team also works with clients and their internal and external counsel to address complex and unexpected business disputes, insurance claims, class actions and associated litigation as well as computer forensic and e-discovery matters. More specifically, our Financial Crime and Anti-Money Laundering team focuses on fraud risk management and regulatory issues impacting financial services and related industries. We work in partnership with our clients to mitigate financial crime risk through enhancements to people, process and technology aspects of their financial crime programs. Enough about us, let’s talk about you You will be working for, or have worked for, a reputable consulting or advisory firm, a regulator (perhaps OSFI or FINTRAC), or a financial institution You will have at least 10 years of relevant experience in the financial crime space, such as AML/sanctions compliance, fraud advisory, forensic investigations etc. You will have completed an undergraduate degree (e.g., in accounting, criminology, law, computer science) and other qualifications such as professional certifications You will have strong viewpoints on financial crime topics, and how developments in this field will impact our clients and the financial services industry ACAMS/CAMS (Certified Anti-Money Laundering Specialist) and ACFE/CFE (Certified Fraud Examiner) preferred Experience with Anti Money-Laundering regulatory compliance work and/or Analytic & AML/Forensic technology is considered an asset Experience in providing insight in fraud prevention, detection and response Strong commitment to professional and client service excellence Superior verbal and written communication skills both in French and English Experienced with project problem diagnosis, solution development, client communications, facilitation of decision making, documentation, managing client expectations and team leadership Canadian travel required, along with occasional international travel. Candidates must be able to enter the USA to work on client assignments. Total Rewards The salary range for this position is $140,000 - $260,000, and individuals may be eligible to participate in our bonus program. Deloitte is fair and competitive when it comes to the salaries of our people. We regularly benchmark across a variety of positions, industries, sectors, targets, and levels. Our approach is grounded on recognizing people's unique strengths and contributions and rewarding the value that they deliver. Our Total Rewards Package extends well beyond traditional compensation and benefit programs and is designed to recognize employee contributions, encourage personal wellness, and support firm growth. Along with a competitive base salary and variable pay opportunities, we offer a wide array of initiatives that differentiate us as a people-first organization. Some representative examples include: $4,000 per year for mental health support benefits, a $1,300 flexible benefit spending account, 38+ days off (including 10 firm-wide closures known as "Deloitte Days"), flexible work arrangements and a hybrid work structure. Our promise to our people: Deloitte is where potential comes to life. Be yourself, and more. We are a group of talented people who want to learn, gain experience, and develop skills. Wherever you are in your career, we want you to advance. You shape how we make impact. Diverse perspectives and life experiences make us better. Whoever you are and wherever you’re from, we want you to feel like you belong here. We provide flexible working options to support you and how you can contribute. Be the leader you want to be. Be the leader you want to be Some guide teams, some change culture, some build essential expertise. We offer opportunities and experiences that support your continuing growth as a leader. Have as many careers as you want. We are uniquely able to offer you new challenges and roles - and prepare you for them. We bring together people with unique experiences and talents, and we are the place to develop a lasting network of friends, peers, and mentors. Our TVP is about relationships - between leaders and their people, the firm and its people, peers, and within in our communities. The next step is yours At Deloitte, we are all about doing business inclusively - that starts with having diverse colleagues of all abilities. Deloitte encourages applications from all qualified candidates who represent the full diversity of communities across Canada. This includes, but is not limited to, people with disabilities, candidates from Indigenous communities, and candidates from the Black community in support of living our values, creating a culture of Diversity Equity and Inclusion and our commitment to our AccessAbility Action Plan, Reconciliation Action Plan and the BlackNorth Initiative. We encourage you to connect with us at [email protected] if you require an accommodation for the recruitment process (including alternate formats of materials, accessible meeting rooms or other accommodations) or [email protected] for any questions relating to careers for Indigenous peoples at Deloitte (First Nations, Inuit, Métis). By applying to this job you will be assessed against the Deloitte Global Talent Standards. We’ve designed these standards to provide our clients with a consistent and exceptional Deloitte experience globally. Deloitte Canada has 30 offices with representation across most of the country. We acknowledge our offices reside on traditional, treaty and unceded territories as part of Turtle Island and is still home to many First Nations, Métis, and Inuit peoples. We are all Treaty people. Job Segment: Compliance, QC, Fraud Prevention, Law, Consulting, Legal, Quality, Security, Technology Apply now » Apply now Start applying with LinkedIn Apply Now Start Please wait... Apply now × Apply for Job × × × Enter your email to apply

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 Bioanalysis for our Bioanalysis team at our Senneville (Montreal West) site, you will be responsible for the design, conduct and reporting of Laboratory Sciences studies efficiently, profitably and with the maximum scientific quality. The Research Scientist scientifically directs the Analysts and other technical staff associated with the conduct, interpretation and reporting of studies. In this role, primary responsibilities include: • Design, write, review and edit, as necessary, 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. • Ensure that projects are performed according to standard operating procedures (SOPs) and Good Laboratory Practice (GLP) regulations, and are aware of regulations published by the FDA, EPA, JMHW and OECD. • Write, review and edit, as necessary, 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 Sponsors on study related business, and generate and distribute Client Interaction Reports (CIRs) in a timely manner. • Ensure the accuracy and completeness of project cost estimates. • Review and approve raw data. • Ensure that a safe working environment is maintained by staff through the observance of safety procedures, the use of protective clothing and equipment, and by the distribution of relevant safety information. Job Qualifications We are looking for the following minimum qualifications for this role: Ph.D., M.Sc. or B.Sc. in chemistry or a related discipline. Depending on educational background, prior experience in the field may not be necessary. Why Charles River ? Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage) Paid development training and annual conferences Employee and family assistance program Access to a doctor and various health professionals (telemedicine) 4 weeks’ vacation & 10 sick/personal days per year Free on-site gym On-site cafeteria 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 supported the development of 86% of the drugs approved by the FDA in 2021. 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. 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 [email protected]. 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.

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 an Analyst for our Laboratory Sciences team located at the Senneville site, you will be responsible for completing technical tasks by following the guidelines of the study plans and Standard Operating Procedures (SOP) and respecting Best Practices Laboratory (GLP). In this role, responsibilities may include: Carry out technical activities as described in the procedures and study plans, while respecting Good Laboratory Practices (GLP). Check the availability and prepare all of the components required for laboratory activities (documentation, samples, solutions, materials, equipment, etc.). Compile appropriate data and submit it in a clear, readable and complete manner. Ensure technical understanding of your work and ensure the smooth running of studies by identifying potential problems, potential solutions and corrective measures to be made. Perform any other related tasks as assigned. Éléments Clés If you have the following qualifications, we will train you for the rest: Holder of a DEC in sciences (biotechnology, medical laboratory or equivalent) or an AEC or a BAC in sciences (immunology, biology, biochemistry) An equivalent combination of education and experience may be considered an acceptable substitute for the specific education and experience as listed above. Ability to work in a team, organizational skills and ability to adapt to changes. Autonomous, meticulous and detail-oriented. Reading comprehension in English is mandatory. Bilingualism in French and English is preferred Position specific information Location: Senneville, Free parking Schedule: weekday schedule, Monday to Friday 8 a.m. to 4:15 p.m. Permanent position from hire, full time 37.5 hours per week Salary: $23/hour Why Charles River Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage) Employee and family assistance program Access to a doctor and various health professionals at all times (telemedicine) 3 weeks of vacation and 5 days of personal leave Numerous organized social activities If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, 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 supported the development of 86% of the drugs approved by the FDA in 2021. 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. 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 [email protected]. 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.

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 an Analyst for our Molecular Biology team located at the Senneville site, you will perform sample analysis work in a laboratory environment, perform data analysis to determine if results meet expectations and record data in accordance with company policies and standards to meet quality and accuracy requirements The Molecular Biology Department mainly analyzes the biodistribution of vectors and cells used primarily for gene and cell therapy. In addition, the team is called upon to analyze the expression of several genes modulated following treatment. The goal of these analyses is to understand the mode of action of different drugs and to determine if they are effective. We work with pharmaceutical compounds that target several therapeutic areas, including oncology, inflammation, infectious diseases, ocular diseases, metabolism, and diseases of the cardiovascular, renal, respiratory and central nervous systems. In this role, responsibilities may include: Perform a variety of DNA and RNA purification assays as well as qPCR and RT-qPCR assays on platforms such as Quantstudio, QXone (ddPCR), Maxwell, Quantigen, and Nanostring. Perform method development, validation and sample analysis testing. Document and process analytical data according to GLP (Good Laboratory Practices) to maintain the company's high level of quality. Work in collaboration with scientific staff to optimize methods. Key Elements If you have the following qualifications, we will train you for the rest: DEC in Science (Biotechnology, Medical Laboratory or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry or equivalent) Ability to work under time constraints, excellent organizational skills, and ability to adapt to change. Work with precision, pay attention to detail, and strive for quality work. Self-starter with a collaborative and positive attitude. Reading and writing English is required. Bilingualism is an asset. Role Specific Information Location: Senneville (Shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site) Free parking Schedule: Weekday schedule, Monday to Friday Permanent position as of the hiring, full time 37.5hrs per week Salary : $23/H Why Charles River? Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage) Employee and family assistance program 24/7 access to a doctor and various health care professionals (telemedicine) 3 weeks’ Vacation & 5 Personal day policy Numerous organized social activities If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, 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 supported the development of 86% of the drugs approved by the FDA in 2021. 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. 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 [email protected]. 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.

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 an Analyst for our Biomarkers team located at the Senneville site, you will participate in the analysis of biological characteristics used to assess disease progression, normal biological processes and pharmacological responses to a drug or mode of action. Our broad scientific expertise covers key toxicology indications and a variety of therapeutic areas including oncology, inflammation, immunology, infectious diseases, and diseases of the cardiovascular, renal, respiratory and central nervous systems. In this role, responsibilities may include: Perform sample analysis based on a variety of immunoassays and enzyme assays such as ELISA, Luminex, radioimmunonalysis, ECL, MSC technology, Simoa technology, and Simple Protein ELLA Oversee method development and perform validation and data analysis to determine if results are as expected, in compliance with Good Laboratory Practice (GLP). Key elements If you have the following qualifications, we will train you for the rest: Holder of a DEC in Science (Biotechnology, Medical Laboratory or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry) Ability to work under time constraints, outstanding organizational skills and ability to adapt to changes. Autonomous, pay attention to details and strive to achieve quality work Reading comprehension in English is mandatory. Bilingualism in French and English is preferred Role Specific Information Location: Senneville (Shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site) Free parking Schedule: Weekday schedule, Monday to Friday Permanent position as of the hiring, full time 37.5hrs per week Why Charles River? Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage) Paid development training Employee and family assistance program 24/7 access to a doctor and various health care professionals (telemedicine) 3 weeks’ Vacation & 5 Personal day policy Numerous organized social activities If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, 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 supported the development of 86% of the drugs approved by the FDA in 2021. 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. 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 [email protected]. 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.