Quality Lab Associate

Cormetech Inc•Cleveland, TN

18d•Onsite

About The Position

We are currently seeking a Quality Lab Associate who would be responsible for testing raw material, catalyst strength, geometry, physical properties, batch characteristics, process audits of workflow, adherence to control plans and procedures and finished goods audits of workmanship. Quality Lab Associates also ensure measurement tolerances for project designs, product appearance, labeling, and packaging. At the heart of clean air, Cormetech is the global leader in the design, manufacture, and full lifecycle management of technologies that clean the air pollutants and carbon dioxide linked to climate change. The company’s reputation is built on three decades of developing and delivering market-leading selective catalytic reduction (SCR) catalysts and CO2 adsorbers, the building blocks of emissions control and CO2 capture systems. If you are looking to make a difference in the world you have found the right place. Join us as we continue to fight climate change.

Requirements

High School diploma / GED required
Associates Degree in a Science field or minimum 2 yrs experience in a laboratory setting
Certification in Mixing, Activation or FGI
Strong communications skills
Ability to troubleshoot problems
Self-motivated, self-starter, able to work independently of direct supervision, assumes ownership of task and drives to completion, detail oriented.
Ability to handle multiple tasks
Experience in MS Office Suite (Word, Excel, Outlook, and Power Point)
Ability to work A/B Team, 12 hour shifts or other assigned hours, depending on production needs.
Dedication to a safe working environment

Responsibilities

Perform testing and data review to product specifications for surface area, element geometry, abrasion, material strength, water absorption, shrinkage, chemistry composition, wet sieve, and other testing as required by internal or external demands
Sample preparation and shipment for offsite testing at offsite plant(s) or 3rd party vendors
Follow established methodologies to produce accurate / reliable data along with performing sensitive measurements that require high precision
Clean and maintain laboratory, testing equipment and quality work area(s) located on the manufacturing floor
Document all activities and record testing results in appropriate electronic and manual files.
Release recycles, incoming raw materials, batches, QP Samples, ON HOLD product, and other components as required
Communicate quality alerts and process audit findings as needed and facilitate / support communication throughout entire organization.
Perform Module Workmanship and PPM audits
Audit processes, set-ups, procedures, control plans
Understand Quality Plan and how to follow it
Write SOP’s, WI’s, PCR’s, DCR’s non-conformances and corrective actions, as needed