Senior Quality Engineer

Medtronic

Confirmed live today High trust

Closes in 5 days

Quick summary

Work type: On-site
Location: Juncos, Puerto Rico
Employment: Full-time
Posted: 3 days ago
Freshness: Confirmed live today
Closes: Oct 2, 2026 (soon)
Nearby: 3 roles within 25 mi

Market check

Salary context

How this pay compares to similar roles

Similar $157k

$118k most similar roles pay here $198k

This listing doesn't post a salary. Most similar roles pay $134,302–$180,500.

Based on 240 similar postings.

Employer

About Medtronic

Medtronic plc is the world's largest medical technology company by revenue, specializing in device-based therapies for over 70 health conditions.

Medtronic currently has 77 open roles on FindRole.

Listed pay typically runs $124,000–$186,000 across 73 roles with salary data.

Most-posted roles

View all roles at Medtronic

At a glance

TL;DR · Senior Quality Engineer

Role Posting Log in to save

Sr Quality Engineer The Sr Quality Engineer provides quality leadership and oversight for manufacturing daily activities, ensuring products and processes meet regulatory, quality, and business requirements. Working with cross-functional teams, the individual manages risk management, product disposition, problem solving, change control, and improvement projects while overseeing equipment and process validation. Daily responsibilities include developing and maintaining quality standards for material processing, designing inspection mechanisms, performing statistical analysis to assess non-conforming products, and ensuring corrective measures meet reliability standards. The role requires expertise in GMP, FDA, ISO 13485, and Quality System Regulations. Key technical skills include Minitab, SPC, trend analysis, Lean Six Sigma methodologies, and knowledge of manufacturing process controls and digital quality systems. This position addresses critical quality challenges within the medical device manufacturing space to ensure high-standard production of healthcare technologies.

Skills

GMP FDA ISO 13485 CAPA NCMR Minitab SPC Lean Six Sigma Data Analytics Quality Systems Process Capability Risk Management Change Control Validation

What you'll do

Provide quality leadership and oversight for manufacturing activities to ensure products meet regulatory and business requirements.
Drive risk management, product disposition, problem solving, change control, and site-wide risk burndown initiatives.
Oversee equipment and process validation activities to ensure operational compliance.
Develop and maintain quality standards and protocols for processing materials into finished products.
Design and implement methods for inspecting, testing, and evaluating the precision of products and production equipment.
Perform statistical analysis to assess costs and determine responsibility for materials that fail to meet specifications.
Ensure corrective measures meet reliability standards and comply with all documentation requirements.
Coach and develop junior Quality Engineers while leading site-wide quality culture initiatives.

What we're looking for

Must have a Bachelor's degree with 4 years experience, a Master's with 2 years experience, or a PhD.
Advanced knowledge of GMP, FDA, ISO 13485, and Quality System Regulations is required.
Experience leading complex CAPA, NCMR, and root cause investigations is required.
Expertise in statistical analysis tools including Minitab, SPC, and trend analysis is required.
Lean Six Sigma Green Belt or Black Belt certification is required.
Knowledge of manufacturing process controls, inspection optimization, and process capability is required.
Knowledge of digital quality systems and data analytics tools is required.
Candidates must possess unrestricted U.S. work authorization at the time of hire.

Save