MSAT Senior Data Scientist (Hybrid) | Houston, TX

small, genuinely improve the world. And that’s the kind of work we want to be part of. Lonza Houston’s Cell and Gene Therapy Facility is the largest in the world and our facility is growing. We are looking for professionals to grow with us and we have an exciting opportunity in the Manufacturing Sciences and Technology (MSAT) department as a Senior Data Scientist.

The Sr. Data Scientist role is a member of the Manufacturing Science and Technology Shared Service (MSAT SS). As such, the individual in this role is responsible for supporting process data analytics (i. e. Global Data Mart) and acting as the Lonza Houston site Global Data Mart Administrator. This role requires direct interfacing

with key stakeholders, in order to identify and implement user requirements, ensure appropriate planning, and execute project tasks, data analysis, manage project risks, providing training and establishing procedures that are necessary for the utilization of the Global Mart / Statistica system.

The incumbent in this role is the project lead who will organize recurring project meetings and is responsible for meeting agenda, minutes, drives overall project execution. Key responsibilities: Serves as the project lead to implement Global Data Mart (GDM) at Lonza Houston, while supporting process data analysis based on the statistical software STATISTICA. Experience with other statistical

analysis software such as MATLAB, Discoverant, Spotfire or others are acceptable.

Collaborates with key stakeholders to gather user requirements for process data track and trending. Leads project team meetings at established frequencies and be accountable for project execution. Serves as the liaison between global support team and the local process teams. Setup web-based data entry templates and analysis configurations to allow for appropriate analysis and enable entry and verification of process data, in compliance with 21CFR Part 11. Performs data entry, as required, data testing and verification. Must be able to complete assignments as instructed, on-time and accurately.

Be actively involved in maintaining high quality data collection systems and continuous improvement. Works with LIMS, Track Wise and PI historian teams, to integrate GDM with these systems, as appropriate. Establishes track and trend objects within GDM for various projects. Provide knowledge and support for validation activities and manufacturing investigations using statistical tools. Performs other job tasks as defined by line manager. Key requirements: Bachelors’ Degree or equivalent in an engineering discipline (biomedical, chemical, biochemical, etc. ), or a life science equivalent.

A Master’s degree in a related field is a plus. Computer/database background is acceptable. Knowledge of statistics and analyses (e. g. ANOVA, T-tests, Regression, Control Charts) Strong knowledge of Statistical Process Control and Continuous Process Verification Understanding of large-scale biotechnology unit operations and GMP requirements Strong leadership skills, capable of distilling complex analyses into easy to understand presentations. Able to communicate status, needs, forecasts, risks and timelines effectively to management. Present information and ideas effectively, formally and informally, verbally and in writing to others in a manner that facilitates understanding.

Displays a clear willingness to listen to others. Has good interpersonal skills and works interdepartmentally in an effective manner to achieve objectives Shows commitment and dedication and strives to be ahead of schedule. Demonstrates ability to find creative solutions to issues and obstacles. Practices safety awareness at all times and considers impact of actions prior to executing activities. Strong computer skills (including Word, Excel, Outlook and Power Point. ), data systems and data analysis; Demonstrates critical thinking skills in problem-solving and decision making; Attention to details and high level of accuracy.

Capacity to motivate and encourage others, in the achievement of specific objectives, and to carry ultimate responsibility. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment.

Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, interaction, interactionual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.