Scientist Bioanalysis 226610
Scientist Bioanalysis 226610
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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 wellbeing 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 well help you build a career that you can feel passionate about.
Job Summary
As a Scientist for our Bioanalysis team located in Senneville you will be responsible for the design conduct and reporting of Laboratory Sciences studies efficiently profitably and with the maximum scientific quality. You will also direct the Analysts and other technical staff in scientific matters associated with the conduct interpretation and reporting of studies.
In this role primary responsibilities include:
- Involved in writing and/or reviewing as necessary study schedules study plans amendments and standalone and contributing Scientist draft and final reports.
- Communicate verbally or in writing with Study Directors and/or Sponsors on study related business and generate and distribute Client Interaction Reports (CIRs) in a timely manner.
- Oversee and coordinate all aspects of study related Laboratory Sciences procedures whether performed within the department or by service departments.
- Familiar with standard operating procedures (SOPs) Good Laboratory Practice (GLP) and regulations published by the FDA EPA JMHW and OECD.
- Review and approve raw data.
- Notify the Principal Director Laboratory Sciences and/or the Associate Scientific Director or Scientific Director / Laboratory Manager of technical problems or deviations from budgeted costs as soon as they become apparent.
Key Elements
We are looking for the following minimum qualifications for this role:
23 years experience with LCMS.
. or . in chemistry or a related discipline with 23 years.
Experience in a GLP environment.
Proficiency in English.
Role Specific Information:
Location: 22022 TransCanada Highway Senneville (QC) H9X 1C1.
Schedule: Monday to Friday.
Why Charles River
- 3 weeks Vacation & 10 Personal day policy
- Competitive benefits as of the hiring. We pay up to 85 of premiums (health & dental coverage)
- Paid development training
- Employee and family assistance program
- Excellent welcome program for new employees as well as inhouse advancement and career development opportunities
- Access to a doctor and various health professionals (telemedicine)
- Many social activities!
If you are interested in contributing to the wellbeing 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 stateoftheart 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 earlystage 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 nonGLP 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 20000 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 clients 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 peoples 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 wellbeing of many across the globe. We have proudly worked on 80 of the approved by the U.S. Food and Drug Administration (FDA) in the past five years.
Were 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 email message to 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 .
Employment Type
Full Time
