Quality Engineer – ISO 13485 / Quality Systems

8 years

0 Lacs

Posted:4 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Candidate from Hyderabad and Pune or someone willing to relocate are preferred.


Summary

We are seeking an experienced Quality Engineer with a strong background in ISO 13485 quality-management systems to support our growing manufacturing operations. The ideal candidate will be proficient in QMS implementation, CAPA management, supplier quality, and process validation within a regulated environment. Experience with injection molding or precision component manufacturing is highly desirable, but the key requirement is the ability to manage and maintain a compliant, efficient, and audit-ready ISO 13485 QMS.


Key Responsibilities

Quality System & Compliance

  • Maintain and improve the company’s ISO 13485-compliant QMS, ensuring documentation control, change management, and risk analysis meet regulatory expectations.
  • Lead internal audits, management reviews, and support external audits (ISO registrar and customer).
  • Ensure compliance with ISO standards and customer-specific requirements.
  • Develop, revise, and approve quality procedures, forms, and records.

CAPA & Non-Conformance Management

  • Lead investigations for non-conformances, customer complaints, and deviations using structured root-cause analysis (5 Whys, fishbone, etc.).
  • Initiate and manage Corrective and Preventive Actions (CAPA) to closure; verify effectiveness and prevent recurrence.
  • Trend quality data and drive continuous improvement using SPC and Lean/Six Sigma tools.

Validation & Process Qualification

  • Author and review IQ/OQ/PQ protocols and validation reports for new processes, equipment, or products.
  • Support risk-based process validation planning consistent with ISO 13485 requirements.
  • Collaborate with engineering to ensure proper documentation of design transfer and production readiness.

Supplier Quality

  • Support supplier qualification, audits, and performance monitoring.
  • Review supplier CoAs, perform risk-based evaluations, and manage supplier corrective actions.
  • Maintain supplier-quality files and ensure incoming materials meet specifications.

Measurement, Inspection & Calibration

  • Support inspection planning, AQL sampling, and FAI documentation.
  • Ensure calibration control and MSA (Gage R&R) for inspection equipment.
  • Review and interpret GD&T on customer drawings; assist inspectors with dimensional analysis.

Documentation & Reporting

  • Prepare and maintain validation summary reports, PFMEAs, control plans, PPAPs, and audit records.
  • Generate quality metrics and dashboards for management review.
  • Provide training and support for operators, inspectors, and engineers on QMS procedures.


Qualifications

Education

  • Bachelor’s degree in Engineering, Quality, or a related technical discipline.

Experience

  • Minimum 8 years of Quality-Engineering experience in a regulated manufacturing environment.
  • Proven expertise in ISO 13485 implementation, audit readiness, CAPA, and risk management.
  • Experience with injection molding, plastics, or silicone component manufacturing is a plus.

Technical Skills:

  • Proficient in QMS software tools, document control systems, and ERP integration (e.g., Odoo, DELMIAWorks, MasterControl).
  • Strong understanding of validation principles, statistical analysis, and data-driven decision-making (SPC, Minitab, DOE).
  • Familiarity with ISO 14971 (risk management) and 21 CFR Part 11 electronic recordkeeping is desirable.

Certifications (Preferred):

  • ASQ Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA).
  • Six Sigma Green or Black Belt.

Soft Skills:

  • Exceptional attention to detail and documentation accuracy.
  • Strong analytical and problem-solving skills.
  • Effective communicator across departments and with customers.
  • Able to thrive in a fast-paced, high-mix manufacturing environment.


Performance Metrics:

  • Timely closure of CAPA and non-conformance actions.
  • Successful ISO and customer audit outcomes.
  • On-time completion of validation and QMS documentation deliverables.
  • Reduction in defects, complaints, and audit findings.

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