GMP Validation Pro: Equipment Qualification & Change Control

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

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.