Do you believe in the power of teamwork and sharing ideas? Do you take pride in delivering exceptional quality and service with everything you do? Do you seek out ideas for improving the status quo?
If you want to make a difference and love being surrounded by the best and the brightest minds, Bureau Veritas Canada might be the place for you!
Here are our Core Values:
Trusted
Responsible
Ambitious & Humble
Open & Inclusive
If these values resonate with you, Bureau Veritas is looking for a
Job Title: Analyst I
Reports to: Laboratory Supervisor/Laboratory Manager
Department: Organics
Location: Burnaby, B.C.
Full time
Basic Purpose:
Responsible for carrying analysis of environmental samples analysis in strict compliance to the requirements of the Standard Operating Procedures (SOP) and Health and Safety policies. Meets quality and TAT specifications required by the client and ensure samples are analyzed within holding time requirements.

Essential Duties and Responsibilities

• Prepare and analyze test samples in accordance with SOPs using complex analytical instrumentation, such as HPLC, GC-MS, GC-FID, LC-MS/MS, ICP-MS, ICP-OES, KoneLab, Automated Titrator etc.
• Perform set-up, calibration and routine/ preventative maintenance of complex analytical instrumentation in accordance with SOPs.
• Process, review, and interpret analytical data. Perform calculations and enter data into LIMS.
• Prepare reagents and standards as per SOPs, and ensure standard verification is performed prior to use.
• Operate and maintain all necessary instruments and equipment to complete tasks (computers, volumetric dispensers, balances, temperature devices, etc).
• Review LIMS summary report to plan and prioritize daily work to accommodate due dates, rush requests, and hold times.
• Provide Supervisor/Manager with updates on workstation status including advance notification of any delays.
• Provide training and direction to junior staff, and ensure training records are completed and maintained.
• Participate in developing, review and revise general WI’s, method SOP’s, FCD’s.
• Perform method validation studies and summarize data for method validation studies in according to SOPs and validation plans, including accuracy/precision, MDLs, MUs etc.
• Participate in internal/external audits, and contribute to investigations/corrective actions.
• Identify and document all known sample deviations, non-conformances, and/or process deviations and report to the Supervisor.
• Employ proper laboratory techniques to minimize risk of mislabeling, sample mix-up and cross contamination between samples and other materials.

Skills and Competencies:

• Science Technical Diploma or B.Sc. or equivalent
• GCMS/FID experience would be an asset
• Strong science background and experience in laboratory practices
• Competent in reviewing analytical procedures and practices
• Excellent interpersonal, verbal and written communication skills
• High degree of accuracy
• Positive outlook with an ability to work in a fast-paced environment
• Good time-management, communication, multi-tasking and priority setting skills
• Ability to adapt to a changing environment
• Ability to work both independently and as part of a team

Education, certifications, and Experience:

• Bachelor’s degree or equivalent preferred
• Experience with gas chromatography-mass spectrometry (GC-MS) instrumentation is preferred

Physical and Environmental Conditions:

• High level of work production in fast paced lab environment
• May require flexible workings hours, overtime and shift work
• Hazardous materials are handled using established safety procedures and appropriate PPE
• Some lifting and carrying

Benefits:

• Health & Dental Coverage
• Life Insurance
• STD & LTD Coverage
• Company RRSP match
• Employee Assistant Program (EAP)
• Professional Development

Bureau Veritas is proud to be committed to providing fair and competitive pay.
The salary range for this role is 24.89 an hour.
Pay within this range varies by work location and may also depend on job-related knowledge, skills, experience, and market location

• Prepare and analyze test samples in accordance with SOPs using complex analytical instrumentation, such as HPLC, GC-MS, GC-FID, LC-MS/MS, ICP-MS, ICP-OES, KoneLab, Automated Titrator etc.
• Perform set-up, calibration and routine/ preventative maintenance of complex analytical instrumentation in accordance with SOPs.
• Process, review, and interpret analytical data. Perform calculations and enter data into LIMS.
• Prepare reagents and standards as per SOPs, and ensure standard verification is performed prior to use.
• Operate and maintain all necessary instruments and equipment to complete tasks (computers, volumetric dispensers, balances, temperature devices, etc).
• Review LIMS summary report to plan and prioritize daily work to accommodate due dates, rush requests, and hold times.
• Provide Supervisor/Manager with updates on workstation status including advance notification of any delays.
• Provide training and direction to junior staff, and ensure training records are completed and maintained.
• Participate in developing, review and revise general WI’s, method SOP’s, FCD’s.
• Perform method validation studies and summarize data for method validation studies in according to SOPs and validation plans, including accuracy/precision, MDLs, MUs etc.
• Participate in internal/external audits, and contribute to investigations/corrective actions.
• Identify and document all known sample deviations, non-conformances, and/or process deviations and report to the Supervisor.
• Employ proper laboratory techniques to minimize risk of mislabeling, sample mix-up and cross contamination between samples and other materials