What are the responsibilities and job description for the Receiving Quality Inspector position at Biomerics?
Company Overview :
Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech industries. As a vertically integrated company, we specialize in the design, development, and production of medical devices for diagnostic and interventional procedures. We are focused on next-generation solutions for the vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart, and cardiovascular markets.
At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to the Biomerics values in all our interactions. It is an exciting time to be part of our collective team. There is no limit to the impact that can be achieved here at Biomerics.
We improve and advance our employees' lives, and the lives of the patients that depend on our products.
At Biomerics we believe in integrity, partnership, empowerment & accountability, trust, agility, teamwork, excellence, and we care. Our team-oriented, customer-focused corporate culture places a premium on building strategic, mutually beneficial partnerships with customers as well as our team members.
Job Description : You will be responsible for Cleanroom-Receiving Quality Inspector, performing the measurement, testing, and visual inspection of various molded components, extruded tubes, medical device assemblies, etc., for production or development / validation activities. The ideal candidate must be able to work in a team-oriented, fast-paced environment. Biomerics is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.
Job Roles and Responsibilities :
- Receive inspected products in the ERP system and label products released for inventory.
- 1st article inspection.
- Review incoming vendor inspection report submissions for completeness and acceptability. Store these records in an established manner.
- Release product for use.
- Perform certain In-process Inspections. Review associated records. Release for further processing.
- Perform Final Functional Quality Audits of the completed product. Review the final instrument. device history file for completeness and acceptability. Store these records in a conventional manner.
- Release product for shipment.
- Assist with the investigation, documentation, and disposition of non-conforming products.
- Any other duties assigned by the supervisor.
Requirements
Requirements
The incumbent must demonstrate the ability to perform the job's essential functions outlined in the duties and responsibilities.
Salary Description
20.72 - $23.99 per hour
Salary : $21 - $24
