Quality Assurance Inspector Ii

Takeda UK

Van Nuys, CA, United States
Base: $21.78 - $34.22; bonus/equity: not specified...
On-site
Perform sampling of chemicals
Conduct physical analysis on chemicals
Handle nonconforming materials
Takeda UK is seeking a Quality Assurance Inspector II for their Van Nuys, CA location. The role involves inspecting chemicals and components used in manufacturing, ensuring compliance with quality standards, and maintaining safety protocols

Job Summary

  • As a Quality Assurance Inspector II, you are responsible for inspection activities for all chemicals and components used in the manufacturing process.
  • You will ensure raw materials meet specifications and reject those that fail to meet quality expectations.
  • This role requires adherence to SOPs and Material Specifications for accuracy and compliance, as well as maintaining data integrity and compliance with FDA and cGMP regulations.

Matching Summary

Match Score: 85

Takeda UK is seeking a Quality Assurance Inspector II for their Van Nuys, CA location. The role involves inspecting chemicals and components used in manufacturing, ensuring compliance with quality standards, and maintaining safety protocols.

Salary

Base: $21.78 - $34.22; Bonus/Equity: Not specified; Benefits: Medical, dental, vision insurance, 401(k) plan and company match, disability coverage, life insurance, tuition reimbursement, paid volunteer time off, company holidays, well-being benefits, sick time, paid vacation

Skills & Requirements

Must-have

  • Perform sampling of chemicals
  • Conduct physical analysis on chemicals
  • Handle nonconforming materials
  • Maintain data integrity
  • Operate powered industrial equipment
  • Adherence to SOPs and Material Specifications

Nice-to-have

  • Attention to detail
  • Organizational skills
  • Effective communication skills
  • General computer knowledge
  • General biotech manufacturing theories

Key Requirements

  • 2+ years of related experience or AA (or equivalent) with no prior experience
  • Familiar with cGMP and FDA requirements
  • Ability to operate in a dynamic, high-paced, cross-functional environment
  • Ability to handle multiple tasks concurrently
  • Intermediate knowledge of laboratory and inspection tools
  • Knowledge of Good Data and Documentation Practices (GDDP), current Good Manufacturing Practices (cGMP), and Environmental, Health and Safety (EHS) requirements preferred

Work Rights

Not specified

Tailored Resume

Cover Letter