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Japanese Quality Assurance Engineer Jobs in Decatur, AL

We provide the advanced engineering, innovative technology, and subject-matter expertise to deliver ... Serve as Quality Assurance specialist for the AFMD Field Maintenance Activity and Warehouse Support ...

This role partners daily with Developers, Product Owners, and Scrum Masters to ensure quality is built in throughout the delivery lifecycle. The Software Consultant, QA influences automation ...

This role partners daily with Developers, Product Owners, and Scrum Masters to ensure quality is built in throughout the delivery lifecycle. The Software Consultant, QA influences automation ...

The QA Inspector reports to the Quality Assurance Supervisor. This position is Monday through ... Receive & understand information provided in the form of Engineering Dwgs, Spec sheets, Parts Lists ...

The QA Inspector reports to the Quality Assurance Supervisor. This position is Monday through ... Receive & understand information provided in the form of Engineering Dwgs, Spec sheets, Parts Lists ...

Cloud Developer

Huntsville, AL · On-site

$55.50 - $75.75/hr

Quality Assurance Engineer Client: US Army POP: 12+ months Location: Huntsville, AL US Citizen REQUIRED SKILLS * Active Top Secret/SCI Eligibility Clearance * At least ten (10+) years of experience ...

Software Consultant, QA Job Location (Short): Madison, United States Workplace Type: Remote Req Id ... Communicate with product developers and technical support specialists on software issues. * Use ...

We offer precision electronic assembly and engineering services to customers with needs-driven, non ... Identify and document defects, non-conformances, and quality issues. * Utilize inspection tools ...

Software QA Intern

Huntsville, AL · On-site

$19 - $25/hr

We are looking for a Software QA Intern to join Vista Robotics, a leading company in the field of computer software and engineering. As a Software AQ Intern, you will play a crucial role in ensuring ...

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Japanese Quality Assurance Engineer information

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How much do japanese quality assurance engineer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for japanese quality assurance engineer in Decatur, AL is $45.51, according to ZipRecruiter salary data. Most workers in this role earn between $35.82 and $52.07 per hour, depending on experience, location, and employer.

What is the difference between Japanese Quality Assurance Engineer vs Software Tester?

AspectJapanese Quality Assurance EngineerSoftware Tester
CertificationsISO standards, QA certifications, ISTQBISTQB, basic testing certifications
Work EnvironmentInvolved in development, process improvement, cross-functional teamsPrimarily focused on executing test cases, bug reporting
Industry UsageManufacturing, software, automotive, electronicsSoftware development, IT companies

The Japanese Quality Assurance Engineer typically has broader responsibilities including process improvement and cross-team collaboration, often requiring specific certifications. In contrast, a Software Tester mainly focuses on executing tests and reporting bugs. Both roles are essential in software and manufacturing industries, but the QA Engineer's role is more comprehensive and strategic.

What job categories do people searching Japanese Quality Assurance Engineer jobs in Decatur, AL look for? The top searched job categories for Japanese Quality Assurance Engineer jobs in Decatur, AL are:
Sr. Director - API Manufacturing Quality Assurance

Sr. Director - API Manufacturing Quality Assurance

Eli Lilly and Company

Huntsville, AL • On-site

$156K - $228K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 71 rated pharmaceutical


Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Lilly is currently constructing an advanced manufacturing facility for production of API molecules. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the leadership team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.
Position Overview
The Sr. Director - QA serves as the Site Quality Leader for the Lilly API site, overseeing manufacturing, utilities, laboratories, and warehousing. This role ensures the strength and continuous improvement of all quality and compliance systems, activities, and personnel. Additionally, the Sr. Director - QA is responsible for maintaining utilities and ensuring that raw materials and drug substances are produced and released in accordance with cGMP standards and marketing authorization requirements.
Key Responsibilities
  • Serve as Site Quality Leader on the Lilly Site Lead Team.
  • Ensure site-wide compliance with cGMPs, procedures, standards, and regulatory commitments.
  • Lead the API Quality Team and manage its agenda.
  • Support quality forums (e.g., Deviation and Change Control Boards).
  • Develop and monitor a site Quality Plan and metrics.
  • Coordinate and manage regulatory inspections.
  • Review and approve manufacturing and quality system documents.
  • Ensure adequate QA staffing and provide coaching and development.
  • Use HR tools for performance management, staffing, and succession planning.
  • Contribute to QA business planning and site-wide strategic planning.

Basic Requirements
  • Bachelor's degree (STEM degree preferred)
  • 10+ years of pharmaceutical manufacturing quality experience
  • 5+ years of supervision/leadership experience

Additional Preferences
  • Experience in Manufacturing, Development, QC, Technical Services, Engineering, or Regulatory Affairs
  • Proficient in statistical analysis and computer applications
  • Strong interpersonal, communication, and networking skills
  • Ability to influence diverse teams and manage multiple priorities
  • Demonstrated problem-solving and analytical thinking

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$156,000 - $228,800
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876