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Assistant Quality Engineer (Whitefield)

SMC Verified employer

Actively hiring · Posted 5d ago · JEV2610B73B6C15C3

SalarySalary not disclosed
Experience2–6 yrs
LocationAll India
Work modeRemote · Full time
Openings1
ShiftWork Location: In person .Other DetailsIndustryMedical / HealthcareRecruiter Det
IndustryMedical / Healthcare

Job description

Position Scope & Purpose

This Position Will be responsible for all the aspects of quality assurance, such as implementing testing & inspection procedures, monitoring the quality of products in each stage of production, collecting data; analyzing the test result; maintaining the measuring & monitoring equipment; generating validation reports; control of the nonconforming products, etc.

Preferred Industry- Medical device, healthcare & automobile industry preferably.

Qualitification- Degree/Diploma in Mechanical Engineering is preferred

Experience-2 to 5 Years Preferred

Communication and Presentation Skills-

Equipment Used-Positive communication skills in English (spoken & written).

Working knowledge of measuring devices like Vision Measurement System, Co-ordinate Measuring Machine, Video Measurement Machine, Digital Caliper, Micrometer, Height Gauge, etc.

Key Accountabilities/Essential Functions

Reviewing of product requirements & specifications such as drawings.

  • Preparing inspection plans, performing metrology activities and preparing FAI reports.
  • Participating in FMEA / Control Plan review and preparing of device master records (DMR).
  • Conducting the measurement system analysis (Gage R&R; ans attribute agreement studies).
  • Issuance and retrieval of documents per control of documents procedure.
  • Maintaining the calibration status of the measuring equipment by periodical tracking.
  • Inspection of incoming raw materials, buyouts & packing materials per receiving quality plans.
  • Issuing supplier corrective action requests (SCAR) and controlling the supplier nonconformities.
  • Performing particle count tests & monitoring of bioburden tests for control of cleanrooms.
  • Inspection of products at start-up, in-process and end-up stages of production.
  • Maintaining of the manufacturing and inspection records in device history records (DHR).
  • Performing final inspections of packed finished goods for product release.
  • Participating in the investigation of non-conformities such as root cause analysis.
  • Preparing 8D report and implementing the corrective and preventive actions.
  • Identifying and retaining the records per control of records procedure.

Technical/Functional Skill Sets

  • Knowledge in programming of CMM & VMM inspection software and associated experience.
  • Knowledge in the process qualification requirements (IQ, OQ & PQ) and experience in validation.
  • Experience in the use of tools of Minitab software such as measurement system analysis (Gage R&R; & attribute agreement studies), process capability studies (CpK & PpK), etc.
  • Working knowledge & experience in implementation of ISO 13485 standard.

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Job Types: Full-time, Permanent

Compensation: 300,[hidden],000.00 per year

Benefits:

  • Food provided
  • Health insurance
  • Provident Fund

Schedule:

  • Rotational shift

Work Location: In person .

Key skills

How to apply

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