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
Supplemental Data
Training and Education
Experience
Knowledge, Skills, and Abilities
Working Conditions and Physical Requirements
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
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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).