Use our `search` to find similar offers.
Laboratory Software Specialist - Validation
Charles River Laboratories International Inc (CRL)
Montreal (Senneville), Quebec, CA, H9X 3R3
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
Job Summary
We are looking for a Software Specialist for our Instrumentation Department located in Senneville (Greater Montreal area) in Canada.
As a software specialist, you will develop your expertise in the area of software support and it is a resource for the technical and scientific sector.
In this role, key responsibilities may include:
• Demonstrate proficiency with procedures and processes related to local software administration, validation and change controls. • Support management of routine requests, such as creating study records or archiving study data with minimal supervision. • Participate in staff training related to the operation of specific software. • Report any problem or potential problems in the conduct of daily activities to the supervisor or delegate. • Participate in software validations in a technical expertise support role [write and execute test script]. • Participate in the maintenance of SOPs for the administration of software and/or those associated with equipment and instruments. • Ensure a safe work environment is maintained by following all work procedures and methods, making proper use of protective clothing and equipment, and reading, understanding and following all documents security issued.
• Ensure documentation associated with systems meets GLP and MVP standards. • Ensure quality work by adhering to applicable departmental policies, practices and procedures [SOPs, security procedures and biosecurity protocols]. • Be flexible with the nature of the work to meet the demands of his group and all other groups in the division. • Ability to work extended hours beyond normal working hours, including but not limited to evenings, weekends, extended shifts and/or overtime shifts, sometimes on short notice. • Performs any other related duties as assigned.
Key Elements
The minimum requirements for the Software Specialist position are:
• Education: CEGEP • Experience: 2 years of related experience • An equivalent combination of education and experience may be considered an acceptable substitute for the specific education and experience as listed above.
Why Charles River:
• Comprehensive group insurance paid 85% by the employer • Paid development trainings • Gym on site, free • Employee and Family Assistance Program • Access to a doctor and various health professionals at all times (telemedicine) • Personal days off • Many organized 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!
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
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 120 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 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 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.
Job posted: 2023-03-16
