QMS Engineer

What to Expect

Gotion is seeking a dynamic QMS Engineer this person will play a critical role in ensuring high quality in production process and output. They are responsible for ensuring control plan implementation, conducting conformance checks, analyzing quality data and driving continuous improvement. Through cross-functional collaboration, they identify and resolve issues in the quality management sustem, ensuring plant operations meet Gotion's standards and customer requirements.

What You’ll Do

• Build a QMS system architecture based on the organizational structure. Establish quality system documents (including quality manual) based on factory requirements and company background, responsible for organizing the related functions for the procedure document cross checking and sign-off, keep running.
• Organize internal quality system audits and management reviews, coordinating with third-party training and certification agency, organizing certification documents submission, and in charge of certification audits until certificate release.
• Identify trends and potential issues and propose preventive measures to reduce risks.
• Organize root cause analysis of quality issues, promote and verify the effectiveness of corrective and preventive measures.
• Develop standard inspection guidelines
• Maintain clear records of all quality activities, including quality reports, audit records, and corrective measures.
• Track industry best practices and quality standards and promotes factory quality systems and process optimization.

What You’ll Bring

• Bachelor’s degree in Engineering

• 3+ years of experience in quality engineering in manufacturing industry, with priority given to those with experience in battery or automotive battery industry. Proven ability to manage multiple events simultaneously and meet tight deadlines.

• Build a QMS system architecture based on the organizational structure. Establish quality system documents (including quality manual) based on factory requirements and company background, responsible for organizing the related functions for the procedure document cross checking and sign-off, keep running.
• Organize internal quality system audits and management reviews, coordinating with third-party training and certification agency, organizing certification documents submission, and in charge of certification audits until certificate release.
• Proficient in quality tools, especially in APQP, PPAP, SPC, FMEA, MSA. Better if familiar with VDA6.3

The U.S. base salary range for this full-time position is $90,000- $120,000, plus eligibility for bonus and benefits. Our salary ranges are determined by factors such as the role, level, and geographic location. The range listed in the job posting represents the minimum and maximum target salaries for this position across all U.S. locations. Actual compensation within the range will be influenced by the specific work location, along with factors such as job-related skills, experience, and relevant education or training. Your recruiter will provide more details about the specific salary range for your preferred location during the hiring process. Please note that the listed compensation reflects the base salary only and does not include bonus or benefits.