Quality - Quality Assurance Inspector I
About The Position
The Quality Assurance Inspector I is responsible to provide general quality assurance support in the areas of inspection manufacturing and assembly. Performs mechanical, electrical and visual inspection of manufactured product and/or processes per documentation (drawings, specifications and procedures) and industry standards. Freedom to act, under supervision, in semi-structured assignments that requires adherence to defined procedures and/or specific, detailed instructions with limited originality. Solves problems of limited scope and complexity. Demonstrates Viant values. This position has the authority to accept or reject materials, subassemblies, assemblies and processes that affect the quality and safety of products. This includes the authority to stop production if necessary to assure that nonconforming products are not released for distribution.
Requirements
- Proficient in knowledge of a variety of testing equipment (pin gauges, snap gauges, micrometer, caliper, etc.).
- Ability to interpret component specifications, drawings and quality procedures.
- Proficient technical writing skills and use of documentation programs (e.g., Office Windows, Excel, Access, PowerPoint, etc.).
- Performs basic arithmetic calculations: add, multiply, subtract, and divide in all units of measure using whole numbers, common fractions and decimals.
- Requires the ability to adjust a microscope lens to bring an object into sharp focus.
- Manual dexterity sufficient to reach/handle items, work with fingers, and perceive attributes of objects and material.
- Requires the ability to identify and distinguish colors and shapes.
- Associates degree or equivalent in work experience.
- English understanding, quality oriented and statistical knowledge.
- 3 months to 1 year of recent experience in medical device industry, with experience of different medical products with as molding operator.
Nice To Haves
- Bachelor Degree in Natural Sciences preferable.
Responsibilities
- Follows all Good Manufacturing Practices and SOP’s as defined by Viant’s policies, practices and procedures to ensure that FDA regulations, GMP, ISO13485, and Viant quality standards are met.
- Checks material disposition and identification in order to meet GMP regulations.
- Inspect and document in-bound raw materials for conformance.
- Collects samples at scheduled intervals from each machine.
- Perform in process dimensional and visual inspection to assure compliance with customer specification giving appropriate disposition according to Viant’s procedures.
- Responsible for documentation of (in-process) sampling plan, disposition and inspection results.
- Perform basic ERP transactions.
- Work on validation projects as needed.
- Manage retains of production and validation projects.
- Audits assigned areas.
- Verifies that the process inspections and areas in charge are in conformance with Viant’s procedures.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
