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Quality Technician - Reagents (C Schedule)

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Location: Salt Lake City, UT, United States
Position Type: Unfixed Term
Job Function: Quality

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A family-owned company, bioMérieux has grown to become a world leader in the field of in vitro diagnostics. For almost 60 years and across the world, we have imagined and developed innovative diagnostics solutions to improve public health. Today, our teams are spread across 44 countries and serve 160 countries with the support of a large distribution network. This includes our SLC site, formerly known as BioFire Diagnostics.

Description

A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety.

In North America we have more than 5,000 team members across 11 sites or subsidiaries, including Salt Lake City-based BioFire Diagnostics and one subsidiary in Montreal, Canada. 

Come and join a family-owned global company with a long-term vision, and a human-centered culture as a
Quality Technician!

Team C schedule: 12 hr night shifts Sunday - Tuesday + every other Wednesday, 6:30 PM - 6:00 AM.

Position Summary:

The Quality Assurance (QA) department provides Quality support across various company departments. The department is organized into distinct subunits, consisting of Metrology, Calibration & Preventive Maintenance, Document Control, Reagent Quality, Instrument Quality, Servicing Quality, and Incoming Material QC.

This is an entry-level position. Depending on the sub-unit, this individual may review quality records, inspect manufactured products and raw materials, perform calibration and preventive maintenance on tools and equipment, and/or maintain Quality system documents. Timely and accurate work is expected.  This position regularly interacts and collaborates with other departments within the company.

 

Principle Job Duties and Responsibilities:

  1. Perform all work in compliance with company policy and within the guidelines of its Quality System.
  2. Responsible for reviewing, assessing and monitoring process and product to ensure compliance to requirements.
  3. May contribute to other Quality Assurance subunits that are outside of their primary Quality Assurance subunit, as assigned.
  4. Inspect product (including labels) to specifications and established procedures. Determine product acceptance status after inspection.
  5. Identify and escalate non-conformances observed during inspection. Work with production teams to resolve non-conformances where possible.
  6. Ensure good documentation practices during quality document and quality record review.  Report inconsistent or incorrect records to appropriate systems.  Work with production teams to resolve erroneous records.
  7. Physically release work in process for finished goods processing.
  8. File and archive quality records according to established processes.

QUALIFICATIONS

Training and Education:

  1. High school diploma or equivalent is required
  2. Knowledge of good manufacturing practices, ISO 9001, ISO 13485, and/or 21 CFR 820 is preferred

Experience:

  1. Minimum 1-year previous on-the-job experience requiring professional communication and interactions utilizing skills outlined below.
  2. Experience in Quality Assurance or Quality Control, laboratory or life science manufacturing setting that has a formal quality system is preferred.

Skills: 

  1. Effective written and verbal communication skills
  2. Proficiency in MS Office tools, including Outlook, Word, and Excel
  3. General computer operation
  4. Attention to detail is fundamental to this position.
  5. Ability to accurately follow written and verbal instructions.
  6. Organization skills as needed to maintain paperwork and task schedule.
  7. Proficiency in internet navigation
  8. Basic math proficiency

Physical Requirements:

  1. Must be able to lift at least 25 lbs and may be required to lift up to 50 lbs.
  2. Must be able to sit or stand for moderate amounts of time and look at computer monitors for an extended amount of time with or without accommodation. Must be able to travel (if necessary).
  3. Must be willing to submit to a color-vision test, though result of the test will not determine employment eligibility
  4. Must be able to perform duties wearing a Powered Air Purifying Respirator (PAPR) as needed.
  5. Must be able to perform duties in a clean room environment. This requires the use of work attire provided and laundered by the company.

BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

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