In Process Quality Engineer

vareximagingΒ· 0547 Varex Imaging Manufacturing India Private Limited
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πŸ“ PuneFull time
Full time0547 Varex Imaging Manufacturing India Private Limited

About this role

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Summary

Your Role –
Production Monitoring: Conduct stage-wise, patrolling inspections on the production floor to ensure adherence to standard operating procedures (SOPs) and control plans.
Inspection & Testing: Use precision measuring instruments (e.g., Vernier, micrometer, height gauge, CMM) to check dimensions, visual appearance, and material properties. Proficiency in reading engineering drawings, GD&T (Geometric Dimensioning and Tolerancing), and using inspection tools.
Defect Analysis & CAPA: Identify, document, and analyze defects, performing root cause analysis (RCA) using tools like Fishbone, 8D, or Why-Why analysis.
Documentation & Reporting: Maintain inspection reports, control plans, and calibration records for measuring equipment.
Process Improvement: Drive continuous improvement initiatives such as 5S, Kaizen, and Statistical Process Control (SPC) to minimize waste and rejections.
Compliance & Auditing: Ensure compliance and support internal/external audits, perform Internal Process Audits.
Quality Tools: Knowledge of 7 QC tools, APQP, PPAP, and FMEA.
Soft Skills: Strong analytical, problem-solving, and communication skills.

Good to Have
β€’ Documents work/deliverables according to the company standards and ISO 13485 and FDA regulations.
β€’ Greenfield Project experience

Job Description

Your Role –

Production Monitoring: Conduct stage-wise, patrolling inspections on the production floor to ensure adherence to standard operating procedures (SOPs) and control plans.

Β Inspection & Testing: Use precision measuring instruments (e.g., Vernier, micrometer, height gauge, CMM) to check dimensions, visual appearance, and material properties. Proficiency in reading engineering drawings, GD&T (Geometric Dimensioning and Tolerancing), and using inspection tools.

Defect Analysis & CAPA: Identify, document, and analyze defects, performing root cause analysis (RCA) using tools like Fishbone, 8D, or Why-Why analysis.

Documentation & Reporting: Maintain inspection reports, control plans, and calibration records for measuring equipment.

Process Improvement: Drive continuous improvement initiatives such as 5S, Kaizen, and Statistical Process Control (SPC) to minimize waste and rejections.

Compliance & Auditing: Ensure compliance and support internal/external audits, perform Internal Process Audits.

Quality Tools: Knowledge of 7 QC tools, APQP, PPAP, and FMEA.

Soft Skills: Strong analytical, problem-solving, and communication skills.

Good to Have

  • Β Documents work/deliverables according to the company standards and ISO 13485 and FDA regulations.
  • Greenfield Project experience

Your Profile:

  • Bachelor in mechanical engineering/Medical Engineering
  • Β 5+years in process quality experience in Automotive or Medical Manufacturing companies
  • Ability to multi-task effectively
  • Proactive problem-solving mindset.
  • Work from Office

SKILLS, KNOWLEDGE AND CERTIFICATIONS

Required Certifications and Training

  • Obtains and completes LMS training plan specific to assigned responsibility.

Experience Level with Business Tools

  • Proficient in utilizing business tools such as:Β  E-mail, Microsoft Word, Excel, and PowerPoint.Β 
  • Experience with SAP or equivalent ERP product and productivity software desired.

LEVEL DESCRIPTION

Knowledge

  • Developing professional skills and experience.

Job Complexity

  • Works on problems of diverse scope where analysis of situations or data requires a review of a variety of factors.Β  Exercises independent judgment and discretion in solving complex business problems.

Interaction

  • Builds productive internal/external working relationships.

Supervision

  • Normally receives general instructions on new projects or assignments.

Typical Education and Experience

  • Bachelors Degree (or equivalent experience)
  • and/or 2-5 years of related experience or Masters Degree with no or little experience.

ENVIRONMENT AND PHYSICAL REQUIREMENTS

Environment and Physical Demands

  • As described in the job posting

Ability to Travel

  • Travel may be required. See the job posting for more information.

Time Type:

Full time

Job Type:

Regular

Work Shift:

N/A

Pay Rate Type:

Salary

All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.

Frequently Asked Questions

Is the salary disclosed for the In Process Quality Engineer position at vareximaging?
The salary for this In Process Quality Engineer role at vareximaging is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the In Process Quality Engineer position at vareximaging located?
This In Process Quality Engineer role at vareximaging is based in Pune. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the In Process Quality Engineer role at vareximaging full-time or part-time?
This is listed as a Full time position. It is posted as a In Process Quality Engineer role in the 0547 Varex Imaging Manufacturing India Private Limited department at vareximaging.
Which team or department does the In Process Quality Engineer at vareximaging belong to?
This In Process Quality Engineer position is part of the 0547 Varex Imaging Manufacturing India Private Limited department at vareximaging. See the full job description for more information about the team structure and responsibilities.
How do I apply for the In Process Quality Engineer position at vareximaging?
Click the "Apply Now" button on this page. You will be redirected to vareximaging's official application portal hosted on workday where you can submit your application directly.
In Process Quality Engineer
vareximaging
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