Sr Quality Technician - Night Shift (D Shift)

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Job description

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Description

A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux provides diagnostic solutions which determine sources 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. Come and join an amazing global company with a solid long-term vision and excellent human-centered culture as a Sr Quality Technician!

Job Summary

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

This position is on the Reagents Manufacturing Quality Assurance (QA) team. This individual will primarily review quality records and inspect manufactured products but may also contribute to other quality functions. Timely and accurate work is expected. This position regularly interacts and collaborates with other departments within the company.

ESSENTIAL 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.
9. Prioritize product release to meet department goals.
10. Control (physically and electronically) material suspected to be non-conforming.

QUALIFICATIONS
Training and Education:

1. High school diploma or equivalent is required.
2. Associate degree (or higher) in a life science or engineering discipline is preferred.
3. 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. Minimum additional 1-year experience in a Quality Assurance, Quality Control, laboratory or life science or other manufacturing setting that has a formal quality system. Education/certification in Quality Management Systems may be used in lieu of this experience.

Knowledge, Skills, and Abilities:

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 push, pull, bend, and/or lift at least 25 lbs, and may be required to lift up to 50 lbs., for extended periods of time on a daily basis.
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.
3. Must be able to travel (if necessary). Minimal domestic travel may be required for training purposes.
4. Must be willing to submit to a color-vision test, though results of the test will not determine employment eligibility.
5. Must be able to perform duties wearing a Powered Air Purifying Respirator (PAPR) as needed.
6. Must be able to perform duties in a clean room environment. This requires the use of work attire provided and laundered by the company.

BioFire Diagnostics, LLC. is an Equal Opportunity/Affirmative Action Employer. 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 BioFire Diagnostics' application process by contacting us via telephone at , by email at email protected , or by dialing 711 for access to Telecommunications Relay Services (TRS).

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