Validation Engineer II

Location: Northern

## Validation Engineer IIApply:
Houston:
Full time:
Posted 30+ Days Ago:
JR100726
*** Join Immatics and shape the future of cancer immunotherapy; one patient at a time!
*** Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of
** PRAME**, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest
** PRAME
* * franchise with the most
** PRAME
* * indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.  
** Why Join Us?**
* ** Innovative Environment:
** Help to pioneer advancements in cancer immunotherapy.
* ** Collaborative Culture:
** Be part of a diverse team dedicated to your professional growth.
* ** Global Impact:
** Contribute to therapies that make a lasting impact on patients globally.
** Role Overview
** We are seeking a
** Validation Engineer II
** to lead the implementation of new systems through the validation process and ensure all validation deliverables and regulations have been met. The Validation Engineer II will build and execute a periodic review program for our validated systems.  
** Schedule**: 8:00 AM – 5:00 PM;
Monday to Friday;
On-site    
** Reports to**:
Senior Director, Enterprise Applications   
** Location**: 13203 Murphy Road Suite 100 Stafford, TX 77477   
*
* Basic Qualifications:

*
* * Bachelor’s degree in Science, Engineering or a related major. Education in Biotechnology or a related major preferred
* 5+ years experience in the pharmaceutical or biotech industry
*
* Preferred Qualifications:

*
* * Experience working within a GxP regulated manufacturing or laboratory environment.
* An understanding of good documentation practices and data integrity principles.
* Demonstrated understanding of 21 CFR Part 11, 21 CFR Part 210, 21 CFR Part 211, GAMP 5 and USP
* Experience in writing and reviewing deviations and CAPAs, investigations leading to change controls
** In this role you will:*
* * Draft validation documents including validation plans, user requirements specification (URS), risk assessments, configuration specification documents, installation qualification (IQ), operational qualification (OQ) and performance qualification (PQ) protocols, trace matrix and summary reports.
* Execute test scripts from IQ/OQ/PQ protocols using good documentation practices and provide appropriate supporting evidence.
* Create and manage project timelines and deliverables.
* Monitor and review Quality Management Systems (CAPA, Change Controls, Deviations) and Batch Record Issuance procedures to ensure and maintain compliance with corporate and regulatory agency requirements.
* Contribute to the writing, coordination, review, and approval of Quality Events when needed.
* Coordinate, support, and investigate Corrective and Preventive Actions (CAPAs).
* Draft SOPs and work instructions for system operation, maintenance, and cleaning.
* Assist in Change Control process from initiation, revision of documents and processes up to training and implementation.
* Assist in preparing QMS training materials and perform training as required.
* Support cross-functional groups for QMS functions and projects not limited to Computer Systems Validation, Equipment Maintenance, Manufacturing, Quality Control, New Hire Onboarding, external and internal audits as needed.
* Perform periodic reviews, requalifications and remediations for systems throughout the system lifecycle.
** What do we offer?
** At Immatics, we believe in investing in our team’s health, safety and well-being. Here’s what you can expect if you join Immatics   
** Comprehensive Benefits**:  
* Competitive rates for Health, Dental, and Vision Insurance
* 4 weeks of vacation, granted up front each year…