Senior Investigational Analyst - Medical Device QA & PM

Kindeva; Missouri; On-site; USD 90,000 - 110,000; Full time

Job summary

Kindeva is seeking a Sr. Investigational Analyst to join the St. Louis Maryland Heights team. This role conducts investigational analysis and testing in the Quality Control Investigational Laboratory, manages protocols and studies, and coordinates testing for auto-injector platforms.

You will work with microscopes, CMM, FT-IR, CT, X-ray, and support project timelines, budgets, and technical reporting, while upholding cGMP, FDA, and ICH guidelines.

Qualifications

• Minimum 1–2 years in a pharmaceutical/medical device laboratory with experience in Quality Control, project management, and investigations.
• Bachelor’s or Master’s degree required.
• Experience with analytical equipment and device development is preferred.

Responsibilities

• Perform testing in the Quality Development Support Laboratory and coordinate testing with others.
• Create initial test documentation and analyze findings, writing technical reports.
• Develop and manage test protocols, timelines, and budgets; provide project summaries.

Skills

Quality Control

Project management

Investigations

Analytical equipment usage

Education

Bachelor’s or Master’s degree

Tools

Microscopes

CT Scanner

X-ray

CMM

FT-IR

Equipment software usage

Job description

Kindeva is seeking a Sr. Investigational Analyst to join the St. Louis Maryland Heights team. This role conducts investigational analysis and testing in the Quality Control Investigational Laboratory, manages protocols and studies, and coordinates testing for auto-injector platforms.

You will work with microscopes, CMM, FT-IR, CT, X-ray, and support project timelines, budgets, and technical reporting, while upholding cGMP, FDA, and ICH guidelines.