Quality Assurance Validation Specialist II
Immatics
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 Quality Assurance Validation Specialist II to support our Global Quality Operations team. The QA Validation Specialist II will be responsible for providing QA oversight of regulated assets and business processes within the Validation Lifecycle Management System (VLMS), ensuring compliance with the Quality Management System (QMS) and GMP requirements. This role will also serve as a Subject Matter Expert (SME) in biopharmaceutical quality and as an on-site QA representative within the U.S. QA Validation team. Schedule : 8:00 AM – 5:00 PM; Monday to Friday; On-site Reports to : Senior Manager, Quality Assurance Validation Location : 13203 Murphy Road Suite 100 Stafford, TX 77477 Basic Qualifications Bachelor Degree in Engineering, Life Sciences, Computer Science or related. At least three years’ experience in a related role. Possess scientific, technical background with experience in Biotechnology, Engineering, Computer Science or related field as well as work experience in related Biopharma industry or similar regulated settings. Advanced understanding of Validation Lifecycle Pillars, which may include equipment lifecycle management, equipment qualification execution, equipment operation, equipment maintenance, workflows incl. GxP Computerized System Validation (CSV), Qualification phases such as IQ, OQ, PQ, Manufacturing Process Validation and Continued Process Verification. Preferred Qualifications: Experience in one or more of the following areas: Quality Assurance (QA) validation within a regulated biopharmaceutical environment. QA release activities within regulated environments. Regulatory audits and inspections. Development, review, and contribution to documentation supporting the testing, validation, and release of Quality Control (QC) and production equipment within clinical and/or commercial GMP environments. Cell and Gene Therapy operations, including clinical and/or commercial-stage environments. Software application deployment, administration, and periodic review within regulated environments. Analytical method validation. In This Role You Will Review and approve asset validation documentation, including User Requirement Specifications (URS), Risk Assessments, Validation Plans, Qualification Protocols, and Validation Reports. Review and approve operational, maintenance, and cleaning (OMC) procedures, ensuring compliance with quality requirements and Good Documentation Practices (GDP). Ensure compliance with applicable regulations and the company’s Quality Management System (QMS). Serve as the QA representative for validation deliverables related to GxP-regulated computerized systems, production equipment, laboratory methods, facilities, and IT infrastructure. Provide QA guidance and best practices based on industry standards and current Cell Therapy practices, including Adoptive Cell Therapy. Collaborate with cross-functional stakeholders to align QA Validation activities with U.S. QA Validation Management, Global Quality Operations, and Site Leadership. Provide QA support for Data Management, Digitalization, Artificial Intelligence (AI), Operational Excellence, Business Continuity, and Archival initiatives. 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 and prorated for first and last year of employment. 12 company paid holidays 7 days of sick time 100% employer-paid life insuranceup to at 1x annual salary, up to one hundred thousand dollars 100% employer-paid short- and long-Term disability coverage 401(k) with immediate eligibilityand company match… The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment. Partially paid parental leavefor eligible employees. Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance. Equal Employment Opportunity We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard torace, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexualorientation, gender identity or expression, national origin, ancestry, age, marital status, disability, geneticinformation, veteran status, or any other status protected by applicable law. Reasonable Accommodations We are committed to providing reasonable accommodations to individuals with disabilities and to applicants withsincerely heldreligious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us View email address on click.appcast.io. Work Authorization Applicants mustbe authorized towork in the United States without the need for current or future sponsorship. Pre-Employment Requirements Employment is contingent upon successful completion of a background check, referencechecksand pre-employment drug screening, wherepermittedby applicable law. For certain roles,additionalscreenings such as a credit check or motor vehicle record review may berequired, where job-related and consistent with business necessity. #J-18808-Ljbffr Immatics
- We’re searching for a Coding Quality Assurance Specialist II — someone who works well in a fast-paced setting. In this position, you will assign and audit the accuracy of the ICD-10-CM and CPT codes to ambulatory, emergency center, observation, and day surgery records for...Suggested
- Quality Assurance Specialist II - Viral Vector Location: Houston, Texas - Onsite Shift: Monday through Friday, 7:30 AM - 4:00 PM As a Quality Assurance Specialist II - Viral Vector, you will serve as a key representative of the Quality Assurance organization, ensuring...SuggestedTemporary workMonday to FridayShift work
- ...SundaythroughThursday,7:00AM-3:30PMAsaQualityAssuranceSpecialistII-ViralVector, you will serve as a key representative of the Quality Assurance organization, ensuring quality and compliance standards are maintained across viral vector and advanced therapy manufacturingoperations...SuggestedFull time
- ...patients globally. Role Overview We are seeking a Validation Engineer II to lead the implementation of new systems through the validation... ...project timelines and deliverables. Monitor and review Quality Management Systems (CAPA, Change Controls, Deviations) and...SuggestedTemporary workImmediate startMonday to Friday
- Creative Solutions Services, LLC is seeking a Validation Engineer II to develop and execute validation protocols for equipment, utilities and facilities at our Houston site. This role supports IQ, OQ and PQ activities and engages with cross-functional teams including Manufacturing...Suggested
- Lonza Biologics, Inc. is seeking a Quality Assurance Specialist II - Viral Vector in Houston, onsite. You will oversee quality for viral vector manufacturing, ensuring cGMP compliance and quality systems integration across manufacturing, QC, and engineering teams. The role...
- Lonza in Houston, Texas is seeking a Quality Assurance Specialist II - Viral Vector to oversee QA for viral vector and cell therapy manufacturing, ensuring products meet quality standards. This onsite role collaborates with Manufacturing, Quality Control, and Engineering...Shift work
- Job-ID32181996Reference26-00479Summary : The Validation Resource for Utilities and Facilities is responsible for ensuring the qualification... ..., including HVAC balancing, environmental monitoring, water quality testing, and cleanroom certification. • Ensure systems meet...Weekend work
- Alcon is seeking an Associate II in Manufacturing Science & Technology Engineering to help develop, implement, and evaluate new production... ...with vendors and partner functions to improve production quality and efficiency. The role requires strong technical knowledge, problem...
- ...role is part of Alcon's Engineering function, a team focused on improving quality, processes, products, packaging and materials across our business to help deliver brilliant outcomes. Associate II, Manufacturing Science & Technology Engineering (Science/Tech/Engineering...Hourly payWorldwideRelocation packageMonday to FridayFlexible hoursDay shift
- Astrion in Houston, TX seeks a Quality Assurance Specialist 2 to support NASA Safety and Mission Assurance by performing inspections to ensure specifications are met. You will inspect mechanical, electrical, and electronic subsystems, witness assembly and test build-ups...
- ...Houston TX Reporting to the Director, Quality Assurance, this position will assist in... ...batch records, QC testing records, validation documentation, and related GMP records... ...coaching, and day-to-day training to QA Specialists I and II and other functional personnel on GMP...Full timeWork at officeShift work
- ...contributions, and challenges you to make a lasting impact every day.Help shape the future of energy infrastructure. As an Engineer II, III, or Senior Engineer - Power Innovation & Project Development, you will support the development of power generation, energy storage...Full timeFor contractorsWork at officeRelocation
- ...We have an exciting opportunity for a Quality Assurance Specialist - Mission Assurance Office to join our... ...assurance activities under the NASA JETS II Contract. This role ensures mission‑... ...storage, calibrated tooling). Validate cleanroom process documentation, ensuring...Hourly payPermanent employmentContract workWork at officeLocal area
- Amentum, NASA JETS II contract partner in Houston, seeks a Quality Assurance Specialist - Mission Assurance Office to ensure mission-critical hardware is processed, inspected, and released in full compliance with NASA, JETS, and Amentum quality requirements. The role supports...Contract workWork at office
- ...and related industries. We're known for fast turnaround, reliable quality, and a strong commitment to helping our customers keep critical... .... Position Summary The Manufacturing Process Engineer II reviews project designs and fabrication drawings to determine efficient...Full timeWork at office
- Job-ID32696496Reference26-01251 Summary : We are looking for a Validation Engineer II with experience in the pharmaceutical or biopharmaceutical industry to join our growing team. Roles & Responsibilities: Develop and execute IQ, OQ, PQ validation protocols and reports...
- We are currently accepting applications for a Project Engineer II to join our Industrial team. (Must be willing to travel based on the needs of the project). Initial assignment is in Beaumont, TX. The Project Engineer I/II is responsible for several functions throughout...Temporary workFor contractorsFor subcontractorWork at officeRelocation
$32 - $35 per hour
...Manufacturing Engineer Location: Houston, TX Duration: 12+ Months Pay Range: $32/hr - $35/hr Lead, execute, document & manage the validation activities (IQ/OQ/PQ) necessary to support the introduction or revision of automated and semi-automated production equipment and...- Quality Assurance Specialist III - Viral VectorLocation: Houston, Texas - OnsiteShift: Sunday through Thursday, 11:00 PM - 8:00 AMAs a Quality Assurance Specialist III - Viral Vector, you will serve as a senior representative of the Quality Assurance organization, ensuring...Full timeTemporary work
- ...Serve as a point of escalation for technical issues within the Quality Management department. Monitor project investigations. Update... ...may assist with field PHMSA document audits. Serve as a lead in Specialist of Construction Quality meetings. Lead training for new...Contract work
- Quality Assurance Specialist IVLocation: This is an on-site position located in Pearland, TX.Available shift: 8:00 am to 5:00 pm Monday through Friday.The Quality Assurance Specialist IV serves as a senior quality representative supporting Cell Therapy manufacturing operations...Full timeTemporary workWork at officeMonday to FridayShift work
$63 per hour
Role: Validation Engineer II Location: 14905 Kirby Drive, Houston, TX - 77047 Contract length: 6+ months with potential for extension... ...with cross-functional teams including Manufacturing, Quality Assurance, Engineering, and R&D. Analyze validation data, identify...Weekly payPermanent employmentContract workShift workDay shift- The Rig Automation Technology Engineer II, within Rig Automation Technology - NCS Engineering & Technical, supports the development... ...suppliers to support field execution, testing, troubleshooting, quality, and project deliverables.Expand technical knowledge through hands...Full timeFor contractorsWork at officeLocal area
- ...seeking qualified candidates to fill the role of a Process Engineer II. Role and Responsibilities Lead new product... ...facing technical representative, collaborating with operations, quality, engineering, and external stakeholders Lead and coordinate Lean...Work experience placement
- Astrix Inc. in Houston, TX, seeks an Injection Molding Process Engineer II to lead development, validation, and optimization of medical-grade molding processes, emphasizing quality, compliance, and efficiency through scientific molding and data-driven improvement. This...Contract work
- ...Laboratory Quality Assurance Specialist The Laboratory Quality Assurance Specialist develops, maintains, and monitors the quality management system for Laboratory Services. Responsibilities include evaluating/implementing patient safety initiatives, regulatory and...
- ...Job Description Job Description Position Summary The Quality Assurance Specialist (QA) is responsible for ensuring Nan & Company Properties maintains high standards of quality, compliance, and efficiency. This role supports agents through compliance oversight,...Monday to Friday
- ...Job Description Job Description Quality Assurance & GMP Compliance Support compliance with Good Manufacturing Practices (GMP), internal procedures, and regulatory requirements. Collaborate with department management to investigate quality issues and develop strategies...
- ...Job Description Job Description Overview Quality Assurance Specialist 2 LOCATION: Houston, TX (Johnson Space Center) JOB STATUS: Full-time CLEARANCE: Currently possess or able to obtain Public Trust CERTIFICATION: N/A TRAVEL: Limited; as needed...Full time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Quality Assurance Validation Specialist II. Be the first to apply!
- quality assurance specialist Houston, TX
- quality assurance associate Houston, TX
- qa associate Houston, TX
- qa specialist Houston, TX
- verification engineer Houston, TX
- validation engineer Houston, TX
- validation consultant Houston, TX
- computer system validation engineer Houston, TX
- senior design verification engineer Houston, TX
- verification & validation engineer Houston, TX


