Test method validation jobs

Supervisor, QC (Chemistry) Method Transfer

Cardinal Health · Posted Nov 9, 2026

Open

Indianapolis, Indiana, United States
$82K–$117K per year
5+ years

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Supervisor, QC (Chemistry) Method Transfer

Cardinal Health · Posted Nov 9, 2026

Open

Indianapolis, Indiana, United States
$82K–$117K per year
5+ years

Apply with Referso

Operations Quality Engineer II

Medtronic · Posted Nov 3, 2026

Open

North Haven, Connecticut, United States
On-site
Full-time · Mid
$79K–$119K per year
2+ years

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Supports Operations Quality function within Advanced Surgical Instruments, ensuring product quality, process performance, and compliance across production operations.

Compensation

Salary ranges for U.S (excl. PR) locations (USD):$79,200.00 - $118,800.00

Responsibilities

Support quality engineering initiatives that improve product quality, manufacturing performance, and quality system effectiveness.
Partner with manufacturing and engineering teams to establish, maintain, and enhance quality standards and control methods.
Develop and implement inspection, testing, validation, and monitoring strategies for products and production processes.
Analyze quality, process, and production data to identify trends, investigate issues, and drive corrective and preventive actions.
Execute root cause investigations and ensure effective implementation and verification of corrective actions.

Requirements

Bachelor's degree
Master's degree
Nice to have: Medical device
Nice to have: pharmaceutical
Nice to have: biotechnology

Skills

Quality System Regulation (QSR)ISO 13485 process validation

Operations Quality Engineer II

Medtronic · Posted Nov 3, 2026

Open

North Haven, Connecticut, United States
On-site
Full-time · Mid
$79K–$119K per year
2+ years

Apply with RefersoAI Apply on careers page

Support quality engineering initiatives that improve product quality, manufacturing performance, and quality system effectiveness.

Compensation

Salary ranges for U.S (excl. PR) locations (USD):$79,200.00 - $118,800.00

Responsibilities

Support quality engineering initiatives that improve product quality, manufacturing performance, and quality system effectiveness.
Partner with manufacturing and engineering teams to establish, maintain, and enhance quality standards and control methods.
Develop and implement inspection, testing, validation, and monitoring strategies for products and production processes.
Analyze quality, process, and production data to identify trends, investigate issues, and drive corrective and preventive actions.
Execute root cause investigations and ensure effective implementation and verification of corrective actions.

Requirements

Bachelor's degree
Master's degree
Nice to have: Medical device
Nice to have: pharmaceutical
Nice to have: biotechnology

Skills

Quality System Regulation (QSR)ISO 13485 process validation

Director, Quality Engineering Production Support

MicroVention · Posted Nov 3, 2026

Open

Aliso Viejo, California, United States
12+ years

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Lead quality engineering initiatives to enhance product quality and compliance for medical device manufacturing.

Responsibilities

Develop and implement strategies to enhance product quality and compliance
Manage team members to lead multiple quality operations projects
Assist executives and senior directors in defining organizational goals and strategic plans
Collaborate closely with manufacturing, R&D, regulatory and other quality areas to support manufacturing process changes
Own product non-conformance procedure and ensure timely execution and closure

Requirements

Bachelor’s degree in a related field of study
Nice to have: Master’s degree in a related field of study
Nice to have: Experience with software used to manage quality information
Nice to have: Experience with the auditing process

Skills

MS Office Suite SAP Minitab FDA medical device quality system requirements ISO medical device quality system requirements

Quality Engineer

Flexible & Integrated Technical Services, LLC · Posted Nov 3, 2026

Open

Ponce, Ponce, Puerto Rico
2–3 years

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Quality Engineer responsible for executing validation protocols, statistical analysis, and ensuring compliance with quality and regulatory requirements in manufacturing and engineering environments.

Responsibilities

Execute validation protocols and qualification activities for equipment, processes, test methods, and manufacturing systems
Develop and execute IQ, OQ, PQ, Process Characterization Studies, TMV, IMV, and DOE
Generate and review validation protocols, reports, and technical documentation
Utilize Minitab for statistical analysis, process capability studies, data trending, and DOE analysis
Support investigations, nonconformance evaluations, corrective actions, and process improvement initiatives

Requirements

Bachelor's degree in Engineering

Skills

IQ/OQ/PQ Protocol Development Process Characterization DOE Methodology Test Method Validation Inspection Method Validation Minitab statistical analysis

Supervisor, QC (Chemistry) Method Transfer

Supervisor, QC (Chemistry) Method Transfer

Compensation

Responsibilities

Requirements

Skills

Benefits

Operations Quality Engineer II

Compensation

Responsibilities

Requirements

Skills

Operations Quality Engineer II

Compensation

Responsibilities

Requirements

Skills

Director, Quality Engineering Production Support

Responsibilities

Requirements

Skills

Quality Engineer

Responsibilities

Requirements

Skills

Benefits

Benefits