Sr MSAT Engineer Apply Now Applied To save a job sign in or get started

Job ID:

10350543 Posted today Back Stafford, TX, US Scientific Bachelors Degree Full Time, Temporary 60 Experienced (Non-Manager) On-site Biotechnology/Pharmaceuticals First Shift (Day) Stafford, TX, US 60 Experienced (Non-Manager) Full Time, Temporary Biotechnology/Pharmaceuticals On-site Scientific Bachelors Degree First Shift (Day) Apply Now Applied Job details Senior MSAT Engineer Kelly® Science & Clinical is seeking a Senior MSAT Engineer for a 12-month contract position at a cutting-edge client in Houston, TX . If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Pay:

$60/hour

Schedule:

Mon-Fri Day Shift Onsite Overview Our client is an industry-leading company at the forefront of cell therapy manufacturing and CMC-GMP operations. This is a unique opportunity to join a cutting-edge organization where you will play a critical role in supporting quality records and PLI inspection readiness within a fast-paced, highly regulated biopharmaceutical environment. In this role, you will be responsible for owning and driving deviations, investigations, and CAPAs from initiation through closure, while partnering cross-functionally with Manufacturing, QA, and other technical teams. You will apply structured problem-solving methodologies, draft inspection-ready technical documentation, and support broader MSAT activities including process troubleshooting, change controls, and continuous improvement initiatives.

Responsibilities:

Own and drive deviations, investigations, and CAPAs from initiation through closure Support execution of PLI-enabling CAPAs and other inspection-readiness quality records Lead root cause analysis, technical impact assessments, and development of corrective actions Draft clear, technically sound, inspection-ready investigation and CAPA documentation Partner with Manufacturing, QA, and other technical functions to drive timely closure of quality records Apply structured problem-solving and risk-assessment methodologies Support broader MSAT activities as needed, including process troubleshooting, process assessments, change controls, manufacturing support, and continuous improvement

Qualifications:

Bachelor's degree in engineering, Life Sciences, or a related technical field 7+ years of relevant biopharmaceutical manufacturing, MSAT, or Process Engineering experience Direct cell therapy manufacturing experience required Strong experience owning deviations, investigations, and CAPAs in a cGMP environment Excellent GMP technical writing and documentation skills Strong root cause analysis and cross-functional problem-solving capability Ability to work independently and manage multiple time-sensitive priorities

Preferred:

Autologous cell therapy experience Late-stage, pivotal, or commercial manufacturing/MSAT experience PLI / inspection-readiness experience Veeva or other electronic Quality Management System (eQMS) experience Houston-area based What happens next: Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless. p#1 10350543 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.

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