Senior Investigational Analyst - Med Device QC & PM Lead

Kindeva; Maryland Heights (MO); On-site; USD 75,000 - 110,000; Full time

Job summary

Kindeva is seeking a Sr. Investigational Analyst to join our St. Louis, Maryland Heights team.

You will perform investigational analysis and testing in QC Investigational Laboratory, manage protocols, oversee studies, and coordinate testing across teams for auto-injector platforms. The role combines project management and engineering expertise, requiring hands-on experience with FT-IR, CT, X-ray, CMM, and related software, plus strong documentation and reporting skills to drive timelines and

Qualifications

• Minimum 1-2 years in a pharmaceutical/ medical device laboratory with experience in Quality Control, project management, investigations, analytical equipment usage, device design or product development.
• Laboratory experience, preferably medical device.
• Bachelor’s or Master’s degree; ability to collaborate and think creatively during investigations.

Responsibilities

• Perform testing in the Quality Development Support Laboratory, coordinating and overseeing additional testing with others as necessary.
• Create initial test documentation including background information, procedures, components, equipment, and data sheets; analyze findings and write technical reports.
• Issuance of NTM, PR and perform root cause analysis as needed.
• Operate FT-IR, CT, X-ray analyses and CMM measurements and manage corresponding software programs.

Skills

Quality Control

Project management

Investigations

Analytical equipment usage

Device design

Product development

Education

Bachelor’s or Master’s degree

Tools

Microscopes

CT Scanner

X-ray

CMM

FT-IR

Job description

Kindeva is seeking a Sr. Investigational Analyst to join our St. Louis, Maryland Heights team.

You will perform investigational analysis and testing in QC Investigational Laboratory, manage protocols, oversee studies, and coordinate testing across teams for auto-injector platforms. The role combines project management and engineering expertise, requiring hands-on experience with FT-IR, CT, X-ray, CMM, and related software, plus strong documentation and reporting skills to drive timelines and