Full Description
QMS Engineer Your Attention to Detail helps for Audits
Job Description:
Responsibilities:
System Compliance: Uphold and upgrade the Quality Management System in compliance with IATF 16949 and ISO 9001:2015 requirements that are particular to plastic parts used in automobiles or medical devices.
Audit Management: Arrange and carry out audits of internal systems and processes. Oversee the closure of Non-Conformance Reports (NCR) and work with outside organizations to arrange certification audits.
Process Control: Create and oversee Quality Assurance strategies, such as Control strategies, documentation for the Production Part Approval Process (PPAP), and Failure Mode and Effects Analysis (FMEA).
Defect Analysis: Use Fishbone diagrams, the 8D methodology, or 5-Why analysis to look into injection molding flaws (such as sink marks, weld lines, or silver streaks).
Supplier Quality: Evaluate and audit raw material (resin/masterbatch) suppliers and secondary process vendors to ensure incoming quality consistency.
Calibration & Testing: Manage the testing of physical
attributes (MFI, Tensile strength, Ash content) and supervise the calibration of precision instruments (vernier calipers, micrometers, CMM).
Corrective and Preventive Action (CAPA) Management: Take the lead in the CAPA process to make sure that manufacturing irregularities are not only corrected but also kept from happening again.
Training: Provide GD&T (Geometric Dimensioning and Tolerancing), statistical process control (SPC), and QMS awareness training to the production and QC teams.
Experience: 3 to 6 yrs
Education: Diploma/BE in Any Specialization
If Interested Please do Send your CV along with you Informations as below to “infohrmaria04@gmail.com”
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Candidate Category: Fresher / Experienced
Willingness to Relocate: Yes / No
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Current/Last Drawn Salary (Monthly/Annual):
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Warm regards,
HR- Maria
88708 33430