GMP Quality Validation - Lab

MEDVACON; Kansas City (MO); On-site; USD 65,000 - 85,000; Full time

Job summary

MEDVACON in Kansas City, Missouri is seeking a Validation Representative to support laboratory validation activities, focusing on Equipment Qualification and change controls. The role requires a Bachelor’s degree or extensive relevant experience, particularly in project engineering and validation of FDA-regulated processes.

Contract duration is one year with an option to extend, working on-site Monday to Friday, 8 AM to 4 PM. Candidates should possess at least 3 years of QA experience in a pharmaceutical environment.

Qualifications

• Bachelor’s degree in a related field or 2-10 years of scientific or engineering experience.
• 3+ years of work experience in project/process engineering and validation.

Responsibilities

• Perform validation for laboratory validation activities.
• Provide technical guidance on validation/process deviations.
• Administer change controls related to validation impact.

Skills

Project/process engineering

Validation of FDA-covered processes

Quality Assurance (QA) experience

Education

Bachelor’s degree in a related field

Job description

Job Description

Validation representative for laboratory validation activities, including Equipment Qualification and systems administration. In addition, provide technical guidance as a SME with respect to validation/process deviations and change controls as pertains to validation impact.

This is a W2 only.

On site.

Shift: M-F 8‑4 PM.

Duration: 1 year with option to extend.

Qualifications

Bachelor’s degree in a related field or 2‑10 years of scientific or engineering experience.

3+ years of work experience in project/process engineering and validation of FDA‑covered processes, as well as QA experience in a pharmaceutical environment.

Benefits

Contract role; no benefits offered.

40‑hour week.

EEO Statement

All of your information will be kept confidential according to EEO guidelines.