Job Description – Manager / Sr. Engineer – Process Quality (IPQA)

Company: Syrma Johari Med Tech
Location: Jodhpur
Industry: Medical Device Manufacturing / Electronics Manufacturing
Experience: 10+ Years
Qualification: B.Tech / B.E. in Electronics, Mechanical, Production, Industrial Engineering
Certification: Six Sigma Green Belt / Black Belt Preferred

About the Company

Syrma Johari MedTech is a leading medical device manufacturing company specializing in design, development, and manufacturing of electronic medical devices with global quality standards including ISO 13485, MDSAP, and US FDA compliance. (Syrma Johari Medtech Ltd.)

Job Summary

We are looking for a highly motivated professional for the role of Manager – Process Quality (IPQA) to drive in-process quality assurance activities, process improvements, defect reduction initiatives, and quality compliance across manufacturing operations. The candidate should have strong exposure to electronics or manufacturing industries with hands-on experience in process quality, root cause analysis, and continuous improvement methodologies.

Key Responsibilities

· Handle end-to-end In Process Quality Assurance (IPQA) activities in manufacturing.

· Monitor production processes and ensure adherence to quality standards and SOPs.

· Drive process improvement and defect reduction initiatives using Six Sigma and Lean methodologies.

· Conduct Root Cause Analysis (RCA) for quality issues and implement CAPA.

· Perform in-process inspections, line audits, and quality checks.

· Coordinate with Production, Engineering, Testing, and Supplier Quality teams for issue resolution.

· Analyze rejection trends, customer complaints, and process deviations.

· Ensure compliance with ISO, GMP, and regulatory quality standards.

· Prepare quality reports, MIS, and process performance metrics.

· Support internal and external audits.

· Train operators and production teams on quality standards and process controls.

Required Skills

· Strong knowledge of IPQA, Process Quality, and Manufacturing Quality Systems.

· Experience in defect analysis, troubleshooting, and process validation.

· Good understanding of CAPA, 5 Why, Fishbone Analysis, FMEA, SPC, and Quality Tools.

· Exposure to electronics manufacturing, PCB/SMT, medical devices, or industrial manufacturing preferred.

· Knowledge of ISO 13485, GMP, or regulated manufacturing environments will be an advantage.

· Good communication, analytical, and team management skills.

Preferred Industry Background

· Electronics Manufacturing Services (EMS)

· Medical Device Manufacturing

· PCB/SMT Manufacturing

· Industrial Manufacturing

· Automotive Electronics

Key Keywords for Sourcing

IPQA, Process Quality, Six Sigma, RCA, CAPA, Process Improvement, Defect Analysis, Quality Assurance, Manufacturing Quality, Electronics Manufacturing, SMT, PCB, Lean Manufacturing, ISO 13485.