MSAT Data & Compliance Coordinator
Confirmed on the employer's own hiring board on Oct 26, 2026. First seen by Alion on Oct 23, 2026. Randstad Sourceright scores B on the Alion truth index.
MSAT Data & Compliance Coordinator
Join our team as an MSAT Data & Compliance Coordinator at Houston TX, supporting clinical-grade Cell Therapy and Viral Vector production through data integrity, process trending, and compliance management to deliver life-changing medicines to patients on a 6-month contract.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Full-time conversion potential based on performance and engagement.
What you will do:
Verify inserted bioprocess data in the Global Data Mart (GDM) at the Lonza Houston site to ensure maximum data accuracy and compliance.
Utilize integrated statistical software (STATISTICA) to support key stakeholders with process data tracking, trending, and Statistical Process Control (SPC).
Assess Vendor Change Notifications (VCN) on raw materials and take ownership of necessary quality change controls.
Initiate material assessments and Part Number (PN) setups within established timelines under direct supervision.
Support Raw Material List (RML) creation in close collaboration with MSAT Scientists, Quality, Procurement, and cross-functional teams.
Actively participate in maintaining high-quality data collection systems and driving continuous improvement across MSAT compliance activities.
Proactively seek operational efficiency and ensure proper planning across assigned tasks while performing additional duties based on business needs.
What we are looking for:
Bachelor’s Degree in Life Sciences, Biotechnology, Data Analytics, or a related discipline required.
1-3 years of relevant experience in biopharmaceuticals, life science laboratory environments, or data compliance within a cGMP manufacturing setting.
Hands-on experience or familiarity with statistical analysis software (e.g., STATISTICA) and centralized data management systems (e.g., GDM, LIMS, or ERP).
Direct exposure to Cell Therapy and/or Viral Vector processes, change control systems, and raw material management is highly preferred.
Strong work ethic, exceptional attention to detail, reliability, and an eagerness to ensure raw data integrity and compliance.
Excellent cross-functional communication skills and the ability to manage competing deliverables in a fast-paced environment.
About Lonza
At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.
As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.
Ready to play your part in shaping the future of life sciences? Apply now.