Quality Technologist (Biotech)

VMRD, Inc.•Pullman, WA

2d•$22 - $28•Onsite

About The Position

The Quality Technologist performs diagnostic assays to assess conformance to company quality specifications and regulatory requirements for products manufactured and provided by VMRD. The work is performed onsite within the Quality Control (QC) laboratory.

Requirements

Treats others with mutual respect and regard
Completes work with accuracy, thoroughness, and a high level of attention to detail while following detailed SOPs
Decisiveness and the ability to work quickly through simultaneous tasks; ability to adjust priorities daily within a dynamic environment
Interest in continual learning with base-level knowledge in molecular biology and immunology
High degree of scientific understanding, curiosity, and dedication to scientific rigor
Solid problem-solving abilities and lab technique (e.g. pipetting, performing dilutions, making buffers)
Written and verbal communication competency
Exhibits constancy and reliability; produces dependable work results
Working knowledge of USDA-CVB, GLP, 9CFR Part 113, and other applicable regulatory bodies
Proficiency with Microsoft Office and adaptability to other software

Nice To Haves

3+ years of experience with quality or manufacturing roles within the biotech industry, ideally focused on diagnostic assays using qPCR and ELISA
Experience with QT9™ QMS software and laboratory information management software systems

Responsibilities

Follows all policies, protocols, regulatory guidelines, and SOPs; Develops and updates SOPs as needed
Efficiently and accurately performs product testing (such as qPCR, ELISA, AGID, IFA, LFD), including completing proper documentation
Generates, performs preliminary analysis, and properly archives data
Calibrates, operates, and maintains critical equipment
Creates and edits QC documents such as COAs and worksheets
Maintains inventory of critical raw materials and supplies necessary for the lab
Proactively coordinates and prioritizes with other departments to meet customer-driven deadlines
Proficiency in performing all regular QC functions independently, after training
At all times, maintains audit readiness of QC's physical and electronic records
Collaborates with cross-functional teams toward achieving business objectives and financial targets by addressing/improving Safety, Quality, Delivery, Cost, and Growth
Contributes to a culture of continuous process improvement
Assist with other duties as needed