CQV Engineer: Lead GMP Validation & CSV

Atp Group; Indiana (PA); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Attractive remuneration packages

Professional development and continuous training

Excellent social security coverage

Job summary

A Life Science compliance firm is looking for a Qualification & Validation Engineer to support clients in complex GMP-regulated projects. You'll plan, coordinate, and execute qualification activities for laboratory equipment and cleanrooms. The ideal candidate has a university degree in Engineering or Sciences, at least 5 years of experience in the pharmaceutical industry, and strong knowledge of GMP regulations. The role offers attractive remuneration and professional development opportunities.

Qualifications

• Minimum 5 years of relevant experience in qualification & validation.
• Fluent in English and German and/or French.
• Experience in facility projects and/or digital quality systems is advantageous.

Responsibilities

• Plan and execute commissioning, qualification, and validation activities.
• Oversee on-site qualification and validation testing.
• Manage small project teams ensuring quality standards.

Skills

GMP regulations knowledge

Analytical mindset

Customer-oriented communication

Project management

Education

University degree in Engineering or Sciences

Tools

MS Office

MS Project

LIMS

TrackWise

SAP

Job description

A Life Science compliance firm is looking for a Qualification & Validation Engineer to support clients in complex GMP-regulated projects. You'll plan, coordinate, and execute qualification activities for laboratory equipment and cleanrooms. The ideal candidate has a university degree in Engineering or Sciences, at least 5 years of experience in the pharmaceutical industry, and strong knowledge of GMP regulations. The role offers attractive remuneration and professional development opportunities.