29 Laboratories jobs in Canada

Job Description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Reporting directly to the BUMa/designee, the Scientific Specialist will be responsible for providing advanced technical support and analysis within the Food Chemistry team for method development, method transfer and routine analysis of raw material, bulk and finished products. This is a deadline-based, high-pressure work environment with on-going projects for a variety of clients. The Scientific Specialist will have experience in handling advanced instrumentation analyses and will be able to work independently with minimal supervision. The incumbent must be energetic, exceedingly well-organized, flexible, and must have the ability to interact with customers and staff in a fast-paced environment, sometimes under pressure, while remaining proactive, resourceful, and efficient. A high level of professionalism and confidentiality is crucial to this role.

The Scientific Specialist must:

• Perform method development, method validation, method transfer and routine analyses using various instrumentation
• Learn and apply knowledge with additional advanced instrumentation techniques (GC-MS, LC-MS/MS, GC, GC-MS/MS, ICP-MS, etc.) and software (ChemStation/OpenLab, Empower, Chromeleon, Analyst, Mass Hunter) as necessary.
• Contribute to all phases of assigned projects, including sample preparation techniques such as extraction and digestion. Set up and change instrument configurations for various LC-MS, GC-MS, ICP-MS methods
• Review data, prepare protocols and reports to ensure testing projects meet the timeline.
• Train new Analysts to perform various techniques
• Perform sample preparation and analysis and execute a number of routine/non-routine methods and procedures including method development, validation, verification and sample testing.
• Perform instrument calibration, qualification and preventative maintenance program as necessary.
• Perform investigations and troubleshoot non-confirmatory results or methods
• Understand and follow Quality System documents relevant to responsibilities, e.g., Quality Manual, SOPs, ISO/GMP/GLP requirements.
• Ensure methods within assigned realm of responsibilities are implemented accurately (per source method or validated laboratory method/SOP).
• Adhere to appropriate quality measures to meet or exceed the standards set by ISO17025, GMP (if applicable), government regulatory and company requirements relevant to assigned duties.
• Maintaining a neat and accurate record system of work performed on a daily basis and as needed for quality control tests or regulatory purposes.
• Guide, mentor and train junior staff members to achieve expected quality and TAT metrics.
• Ensure turnaround time goals are met or exceeded.
• Cleaning of lab ware and decontamination as needed.
• Media preparation and storage if needed.
• Any tasks as required by supervisor or Management in all aspects of business to meet the monthly R&D targets.

General Qualification :

• Work competently without direct supervision while applying technical laboratory skills.
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
• Experience in developing new methods and method transfer validation.
• Must be able to handle all kinds of samples.
• Carry out sample preparation procedures and analyses.
• Take and follow directions accurately.
• Strong computer, organizational skills.
• Clear verbal and written communication skills.
• Skilled in data/report generation, retrieval and interpretation of routine analysis.
• Experienced in the operation, routine maintenance and troubleshooting of specified instrumentation or equipment.
• Perform other related duties as assigned.

Specific Desired Experience

• 6+ years working with applied chemistry techniques;
• At least 1-3 years of experience in LC-MS, GC-MS, ICP-MS with hands-on experience in chromatographic separation and mass spectrometry techniques
• Experience working with organic matrices (preferably food);
• Experience working in a contract laboratory considered an asset.

Technical Skills:

• Good computer skills - proficiency with MS Office;
• Working knowledge of Laboratory Information management Systems (LIMS).

EDUCATION

• A B.Sc. degree preferably in Chemistry, or diploma in related field;
• A solid background and understanding of Chemistry is mandatory;

WORKING CONDITIONS

• This position is working in a laboratory environment where standing is required for greater than 50% of the time to work at the bench for analyses.  Light lifting requirements of no more than 20 lbs.    Hazardous materials are handled using established safety procedures and appropriate PPE.  Some lifting and carrying (up to 10 kg).

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at 

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at 

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

NO AGENCIES, CALLS OR EMAILS PLEASE

Job Description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

The Analyst will be responsible for providing technical support and analysis within the Cannabis Chemistry Testing Laboratory. This deadline-driven, high-pressure environment involves ongoing projects for a variety of clients. The role requires strong organizational skills, technical proficiency, and the ability to work independently with minimal supervision.

• Perform routine and non-routine wet chemistry methods and procedures

• Prepare samples and mobile phases accurately following SOPs

• Retrieve, analyze, and interpret technical data and routine test results

• Write and review lab reports, SOPs, and laboratory documentation

• Troubleshoot instrument and method-related issues effectively

• Assist with method transfer, verification, and validation processes (primarily Analyst II)

• Operate and maintain laboratory instrumentation (e.g., HPLC, GC, ICP)

• Provide technical support to R&D and customer service teams, including training and staff development (primarily Analyst II)

• Maintain excellent customer relations by working directly or indirectly with clients

• Conduct system qualification, calibration, and general lab duties under GMP and GLP guidelines

• Ensure compliance with USP and pharmaceutical testing standards

• Document all procedures and results accurately in lab notebooks

• Adhere to safety protocols, including use of PPE and proper handling of hazardous materials

• Work in a collaborative, fast-paced environment, sometimes under pressure and tight deadlines

• Perform administrative tasks as assigned

• Education: B.Sc. in Chemistry or related field preferred; diploma considered for Analyst I

• Experience:

  • Analyst I: 2 years' of experience in instrumentation analyses with ability to work independently

  • Analyst II: 5 years’ experience operating instruments including HPLC, GC, ICP; experience with cannabis or natural health products an asset

• Skills:

  • Proficient in Microsoft Office, especially Excel

  • Excellent organizational, verbal, and written communication skills

  • High attention to detail and accuracy

  • Ability to multitask and remain calm under pressure

  • Proactive, self-disciplined, and able to demonstrate high productivity

  • Strong troubleshooting skills in both instruments and methods

  • Ability to learn quickly and apply knowledge effectively

Key Personal Attributes:

• Energetic, well-organized, flexible, and professional

• Ability to interact effectively with customers and staff in a high-pressure environment

• Maintain confidentiality and demonstrate a high level of professionalism at all times

WORKING CONDITIONS This position is working in a laboratory environment where standing is required for greater than 50% of the time to work at the bench for analyses. Light lifting requirements of no more than 20 lbs. Hazardous materials are handled using established safety procedures and appropriate PPE. Some lifting and carrying (up to 10 kg). Extra hours, weekends and evenings will be required.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at 

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at 

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

NO AGENCIES, CALLS OR EMAILS PLEASE

Job Description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Initial training for this position will take place in Toronto, ON.

• Demonstrates and promotes the company vision.
• Ensures regular attendance and punctuality.
• Reads, understands, and follows management system requirements relevant to responsibilities, including but not limited to requirements found in the Quality Manual, SOPs, Local Work Instructions, and Methods. This ensures compliance with ISO/IEC 17025/AOAC ALACC requirements and relevant government regulatory requirements.
• Adheres to all health, safety, and environmental regulations relative to assigned analytical work; maintains and assists others in maintaining a clean, safe work environment.
• Registers incoming samples as needed, maintains a neat and accurate record system of work performed on a daily basis, and as needed for quality control tests or regulatory purposes.
• Enters sample data into Eurofins eLIMS system in a timely and accurate manner.
• Completes laboratory testing on all incoming samples accurately, efficiently, and in a timely manner; ensures sample turnaround time goals are met or exceeded.
• Verifies results and submits them to the appropriate personnel for transmission in a timely manner.
• Identifies process difficulties and reports these, along with proposed solutions, to the supervisor.
• Maintains a perpetual state of readiness and willingness to respond to the queries and needs of clients, staff, and co-workers.
• Maintains cooperative working relationships with all company employees. Communicates orally and in writing to co-workers, including intra- and inter-departmental employees.
• Promotes the company image through the exercising of sound and ethical business practices related to the public and our customers.
• Continually strives to improve the quality of work provided to clients through existing and new technologies.
• Identifies non-conformances and out-of-specifications.
• Conducts all activities in a safe and efficient manner.
• Performs other duties as assigned.

• 1–2 years of microbiology laboratory experience required.

• Excellent interpersonal and organizational skills.

• Excellent communication skills.

• Responsive problem solver and action-oriented.

• Basic computer literacy.

• Laboratory safety and WHMIS training.

• Troubleshooting skills required for instrument maintenance.

• Technical knowledge of applicable test methods.

• Willingness to work overtime, weekends, and holidays.

Working Conditions:

This is a laboratory environment with the majority of time spent standing and working at a lab bench. Hazardous materials are handled using established safety procedures and appropriate PPE. Lifting requirements may apply. Extra hours, weekends, and evenings may be required as per business needs.

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at 

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at 

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

NO AGENCIES, CALLS OR EMAILS PLEASE

Job Description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Under the direction of the Research & Development Manager, Analyst III (LC-MS/MS or GC-MS/MS) will be responsible for supporting the department through coordinating research activities directed toward the development of new methods and conducting validations that meet the departmental goals. The position is instrumental in the development/validation of a new test method as per ICH guidelines.

Key Responsibilities:

• Write Assay & Impurities method development  & validation protocol and report
• Perform method validation/routine analysis using LC-MS/MS or GC-MS/MS.
• Review technical data, documents, and proposals as required.
• Troubleshoot technical issues/ difficulties with methods.
• Carry out and support OOS/OOT investigations;
• Co-ordinate method transfers study between clients and other departments.
• Assist SOP training for new personnel and on SOP revisions.
• Liaison with clients as needed to maintain superior relationships.
• Provide ongoing technical training and develops staff to enable them to perform technical tasks.
• Support Department Head of R&D in all aspects of a business to run the department smoothly.
• Minimum 3 years’ experience with GCMS/MS with Masshunter software
• Troubleshoot the GCFID and GCMS detector

Education:

• Degree or diploma in Chemistry or related discipline; MSc. would be an asset
• 3+ years working with LC-MS/MS or GC-MS/MS
• 5-10 years experience working in Cannabis, Pharmaceuticals or NHP Laboratory
• Experience working in a contract laboratory is an asset

Other Required Skills:

• Excellent organizational skills
• Strong verbal and written  communication skills
• High level of accuracy and strong attention to detail
• Ability to work independently or in a team environment
• Must be able to work in a fast-paced environment

WORKING CONDITIONS

This position is working in a laboratory environment where standing is required for greater than 50% of the time to work at the bench for analyses.  Light lifting requirements of no more than 20 lbs.   

Hazardous materials are handled using established safety procedures and appropriate PPE.  Some lifting and carrying (up to 10 kg).

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at 

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at 

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.

NO AGENCIES, CALLS OR EMAILS PLEASE

Job Description

Salary:

Closing date: Hiring multiple candidates - Will remain open until suitable candidate found

Salary: Commensurate with experience

Benefits: Health/dental plan, employee & family assistance program, retirement plan, perks

Start Date: Jul/Aug 2025

Primesite Research Solutions is an Integrative Research Organization and Site Network based out of Western Canada. We conduct phase I, II, III, IV clinical trials in various clinical areas at local hospitals and clinics. We are seeking a research assistant to join our growing site network. This position requires a self-motivated, organized, and accountable individual with strong attention to detail. The applicant must have the ability to prioritize and multi-task in a complex rapidly changing environment and must be able to promote teamwork, collaboration, and problem-solving skills. In this position the research assistant will work under the supervision of the research coordinators and research manager to fulfill clinical trials related responsibilities and ensure that each study progresses efficiently. The research assistant will also be responsible for data entry and management of selected patient registries. This position requires frequent contact with physicians, other staff, study participants, biopharma companies and regulatory agencies, and has significant potential for advancement.

Key Responsibilities :

• Adhere to multiple research protocols, confidentiality, ICH, GCP & NIH guidelines
• Prepare REB submissions and other regulatory documents required for study initiation
• Perform data entry for clinical trials and registries
• Prepare for and participate in monitoring visits and conference calls
• Develop study files in accordance with various protocols
• Provide administrative support including filing, directing phone calls, updating tracking logs and maintaining trial regulatory documents
• Organize and maintain project/task management system and clinical trials management system (CTMS)
• Organize, prioritize and respond appropriately to incoming correspondence
• Maintain optimal office systems, processes and equipment
  
• Coordinate with various departments and correspond with study sponsors and regulatory agencies
• Communicate study procedures and provide ongoing support to staff
• Screen hospital charts for potential study participants and be able to discuss eligibility with research coordinators and physicians
• Organize ongoing patient follow up and study visits
• Perform study procedures (including collection of vital signs, blood, ECGs etc) as requested
• Comfortable handling and transporting blood, marrow and other lab samples
• Travel between hospitals for various tasks
  
• Work effectively with study research coordinators and manager to ensure open communication and efficient prioritization of all assigned responsibilities

Required Skills for Success:

• Undergraduate degree required, patient interaction and clinical trials experience are preferred (other education with clinical research experience will be considered)
• 2-3 years of experience in working with clinical trials/research studies
• Must be comfortable interacting directly with patients
• Working knowledge of Microsoft Office software (Word and Excel) and Google Apps (Docs and Sheets) required
• Tech savvy, willingness to learn and adapt to new technologies, and ability to proficiently use required technologies and applications: online software including for meetings, training, timesheets, project/task management, document management and CTMS
• Excellent organizational, communication (oral and written), problem solving and interpersonal skills in dealing with co-workers, clinicians and study participants
• Demonstrated ability to take initiative and work in a team environment as well as independently with minimal supervision in a fast-paced environment
• Ability to be flexible, assist on multiple projects and successfully prioritize multiple responsibilities to meet deadlines
  
• Work in a professional and ethical manner in accordance with internal policies and procedures, and GCP and ICH guidelines
• Self-directed, proactive attitude, highly self-motivated and enthusiastic
• Accountable with strong attention to detail and honest in the performance of all responsibilities
• Willingness to further professional knowledge by reading journals/books, attending educational sessions, completing training programs as necessary
  
• Own transportation and valid driver's license are beneficialas travel to other sites may be necessary

If you are selected for the next step in the interview process, you will be asked to submit a short one-way video application.

English

• Computer and information sciences, general

Work must be completed both in person and remotely.

English

Work must be completed at the physical location. There is no option to work remotely.

Job Description

Salary:

The Akausivik Inuit Family Health Team (AIFHT) is a not-for-profit health clinic dedicated to delivering culturally competent, high-quality care to the Inuit community. AIFHT works collaboratively with federal, provincial, and local health authorities to ensure we are responsive and rooted in a model of excellence in primary care.

AIFHT is currently looking for a Research Assistant/Associate to join our team in a one-year term position (with the potential for extension). The Research Assistant/Associate will support health research activities led by our organization. This includes gathering data, preparing, and distributing surveys, supporting stakeholder engagement, and assisting in other research-related tasks. This role will be based in a medical setting and will involve both administrative and field-based research responsibilities.

The position reports to the Executive Director and receives day-to-day guidance and support from the Research Project Manager.

KEY RESPONSIBILITIES:

• Assist with the collection and management of research data.
• Conduct interviews with survey or study participants.
• Participate in consultations with stakeholders (including Inuit participants and organizations at local, regional, and national levels).
• Prepare meeting materials, schedule sessions, and take meeting minutes as needed.
• Maintain accurate and confidential records, including research and participant files.
• Assist in drafting reports, summaries, and research documentation.
• Support overall research team coordination and communication.
• Perform other related duties as assigned.

QUALIFICATIONS & EXPERIENCE:

• Post-secondary education in Health Research, Social Sciences, Office/Project Administration, or equivalent combination of training and experience.
• 1 - 2 years of experience in research or administrative roles (related experience is considered an asset).
• Strong written and verbal communication skills.
• Proficiency with Microsoft Office, internet-based research tools, and basic data management.
• Knowledge of Inuit health-related challenges in a cultural context.
• Highly organized and able to manage multiple tasks in a dynamic, client-facing environment.
• Fluency in Inuktitut is a strong asset.

WORKING CONDITIONS:

• May be required to work occasional evening or weekend shifts depending on project needs.
• This is a full-time, term position with potential for renewal based on funding and performance.

APPLICATION DETAILS:

Preference in hiring will be given to qualified candidates with Inuit Ancestry as directly relevant to the skills and knowledge for this position. The successful candidate will be required to submit a Criminal Record Check, with Vulnerable Sector Screening.

Only those selected for an interview will be contacted. We thank all applicants for their interest.