Sr Quality Technician (A Shift)

4 Days ago • 1-2 Years

Job Summary

Job Description

The Quality Assurance (QA) department supports various company departments, with subunits in Metrology, Document Control, Reagent Quality, Instrument Quality, Servicing Quality, and Incoming Material QC. The role involves reviewing quality records, inspecting products, performing calibration, and maintaining documents. This position requires self-direction and collaboration with other departments. Responsibilities include ensuring compliance, assessing products, and potentially contributing to other QA subunits. The role demands attention to detail, following instructions, and maintaining paperwork. The individual will also release work in process, file records, and prioritize product releases. They will also report floor failures, review records, and release finished goods. In addition, the person will confirm that the manufacturing equipment meets requirements.
Must have:
  • Review and assess process and product compliance.
  • Follow company policy and Quality System guidelines.
  • Effective written and verbal communication skills.
  • Proficiency in MS Office tools, including Outlook, Word, and Excel.
  • Minimum of 1 year of on-the-job experience.
Good to have:
  • Associate degree in a life science or engineering.
  • Knowledge of good manufacturing practices, ISO 9001, ISO 13485, and/or 21 CFR 820 is preferred.
  • Perform duties wearing a Powered Air Purifying Respirator (PAPR) as needed.

Job Details

Position Summary

The Quality Assurance (QA) department provides Quality support across various company departments. The department is organized into distinct subunits, consisting of Metrology, Document Control, Reagent Quality, Instrument Quality, Servicing Quality, and Incoming Material QC.  Depending on the sub-unit, this individual may review quality records, inspect manufactured products and raw materials, perform calibration and preventative maintenance on tools and equipment, and/or maintain Quality system documents. Timely and accurate work is expected.  This position builds upon the skills and responsibilities of a Quality Technician and requires an increased level of self-direction and motivation. This position regularly interacts and collaborates with other departments within the company. 

Primary Duties  

  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. Other Duties – see relevant Appendix section

Supplemental Data 

  1. Minimal domestic travel may be required for training purposes  

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 required.  

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.

Working Conditions and 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).

 Proficiently:

a. Inspect product (including labels) to specifications and established procedures. Determine product acceptance status after inspection.

b. Identify and escalate non-conformances observed during inspection. Work with production teams to resolve non-conformances where possible.

c. 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.

d. Physically release work in process for finished goods processing

e. File and archive quality records according to established processes.

f. Prioritize product release to meet department goals

g. Identify and report floor failures observed during sweeps of manufacturing areas.

h. Review and approve Device History Records.  

i. Receive and hold finished goods inventory until release is authorized

j. Release finished goods to stock inventory k. Coordinate molded part validation inventory

l. Confirm manufacturing equipment meets requirements for release to Manufacturing Engineering for validation.

m. Confirm manufacturing equipment meets specifications for release to Reagent Manufacturing for use.

n. Control (physically and electronically) material suspected to be non-conforming Physical Requirements

  1. Must be willing to submit to a color-vision test, though result of the test will not determine employment eligibility
  2.  Must be able to perform duties wearing a Powered Air Purifying Respirator (PAPR) as needed.
  3.  Must be able to perform duties in a clean room environment.  This requires the use of work attire provided and laundered by the company.
  4.  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. 

Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at recruitment@biomerieux.com.

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 recruitment@biomerieux.com, or by dialing 711 for access to Telecommunications Relay Services (TRS).

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