Laboratory Analyst 1 - RCAp

at  Company Bureau Veritas

Bedford, NS, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Nov, 2024Not Specified22 Aug, 2024N/AGood communication skillsNoNo
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Description:

Laboratory Analyst 1 - RCAp
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Date: Aug 13, 2024
Location: Bedford, Nova Scotia, CA
Company: Bureau Veritas
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, Bureau Veritas Laboratories might be the place for you!

IMAGINE BEING SURROUNDED BY THE BRIGHTEST MINDS IN THE INDUSTRY.

Bureau Veritas is looking for an

How To Apply:

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Responsibilities:

  • Follow Standard Operating Procedures.
  • Ensure that working records are completed and raw data is appropriately labelled.
  • General housekeeping of laboratory and workstations.
  • Prepare and clean glassware required for reagent and standard preparation.
  • Organizing and preparing the samples to be analyzed on the Discrete Analyzer instruments to ensure client required deadlines are met and to prioritize RUSH samples to meet client requirements.
  • Creating LIMS worksheets for each test being done and assigning the samples to the worksheets plus required QC samples. Where in place, adding the traceability code for each reagent and standard used for the samples to the individual worksheets.
  • Preparing the required calibration standards, QC samples and reagents as outlined in the individual SOPs. Documenting the standard and reagent preparation details in the Reagentc module in the MaxxLIMS Applauncher.
  • Performing daily instrument calibration for each test being performed and carrying out the required instrument maintenance activities. Filling out the Maintenance Log for each instrument on a daily basis.
  • Reviewing the analytical data while an analysis run is in progress to ensure sample results are acceptable for reporting, this includes ensuring that the results for QC samples meet data acceptance criteria as outlined in the individual SOPs and initiating any required corrective actions or repeat sample analysis as required.
  • Documenting non-conformances in Bench Level Non-Conformance Log and notifying senior staff of non-conformances for sign-off and approval.
  • Uploading and reporting the sample results into LIMS worksheets and entering the results for the QC samples Laboratory Control Samples (Blank Spikes) into each individual control chart.
  • Perform simple analysis, including operation of balances and pipettes.
  • Meet quality and turnaround time specifications required by the client and ensure samples are analysed within holding time requirements.
  • Provide supervisor with updates on workstation status including advance notification of any delays.
  • Maintain control charts as per QA manual requirements, monitor for failure to meet tolerances and consult with Supervisor regarding remedial action.
  • Standard laboratory environment
  • Availability for shift work, OT and weekend work required
  • Other duties as assigned

You are the ideal ANALYST 1 if:

  • You have a technical diploma, B.Sc. preferred
  • Knowledge of standard operating procedures and instrumental techniques

Attributes:

  • Basic laboratory cleanliness skills
  • Good analytical laboratory skills
  • Good organizational skills
  • Good multi-tasking abilities
  • Good independent worker
  • Good written and oral communication skills
  • Ability to work as part of a team
  • Ability to work under pressure to meet challenging deadlines

Bureau Veritas is a world leader in testing, inspection and certification services.
When we look at Bureau Veritas, we want to see a reflection of the communities in which we work. Inclusion is about actively involving every employee’s ideas, knowledge, perspectives, approaches and styles to maximize business success. Inclusion is about attracting new talent who will bring more diversity to our workforce, with differences in culture, professional backgrounds and beliefs.
Our purpose: shaping a world of trust.
Guaranteeing quality, ensuring Health and Safety, mitigating risks and improving performance as well as environmental protection and social responsibility … This is what Bureau Veritas is about, truly believing that it contributes to bettering society.
Blending performance & integrity, with ambition & humility, responsibility & openness, we are proud that our people leave a mark on what they do.
We respect our people and believe in our talents.
We empower them to leave their mark, working as a team for the benefit of our 400,000 clients across 140 countries.
We believe that leaving a mark is a true challenge and opportunity for every one of us, a sign of trust and impact, a bond with the future, a proof of growth and development.
Being part of the BV family, is more than just working, it’s being convinced that you will Leave your mark…. in shaping a world of trust.
Join our talented community of scientists and experts and apply today at https://www.bvna.com/careers
Bureau Veritas Labs is an equal opportunity employer. We are committed to an inclusive, barrier-free recruitment and selection process and work environment. If you are contacted for a job opportunity, please advise Human Resources of any accommodations that are required. Any information received relating to accommodations will be treated as confidential.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Information Technology/IT

Pharma / Biotech / Healthcare / Medical / R&D

Other

BSc

Proficient

1

Bedford, NS, Canada