The University of Texas MD Anderson Cancer Center
MSAT Associate II, Materials Science and Technology
The University of Texas MD Anderson Cancer Center, San Diego, California, United States, 92189
Job Title:
MSAT Associate II, Materials Science and Technology
Job Number:
83464
Location:
San Diego, US
Salary:
$75-95K
Job Description:
We are seeking a motivated, science-oriented individual with proficient knowledge of GMP manufacturing and an understanding of cell culture/cell therapies.
Responsibilities
The Materials Science and Technologies (MSAT) Associate II will need to learn/train quickly to provide Subject Matter Expert (SME) feedback for the various manufacturing processes.
This position will support CMC operations focusing on process development/optimization, technology transfers, change controls, manufacturing operations, and creation or revision of controlled documents.
Providing support to the MSAT Team and working cross-functionally to ensure clear communication across various departments.
Training on the cell therapy platforms quickly to assist in compiling scientific data relating to the cell therapy and new platforms.
Assisting with all tech transfers into cGMP Manufacturing, ensuring the transfer is controlled and executed within GMP regulatory guidelines.
Supporting the Manufacturing group and troubleshooting production activities to ensure safe, quality, and timely manufacture of biopharmaceutical products for pre-clinical, clinical, and commercial use.
Creating or revising (as needed) and reviewing all process-related manufacturing documentation (batch records, SOPs, bills of material, tech transfer documents, risk assessments, and process flow diagrams) to assure all clinical products meet the requirements for quality, safety, and efficacy.
Performing manufacturing deviation investigations to help determine root cause and product impact.
Providing in-person and real-time manufacturing production support as needed.
Identifying process improvement opportunities and/or corrective actions to increase yield, maximize capacity, improve operational efficiency, reduce costs, and ensure safety while maintaining regulatory compliance in collaboration with Research and Product Development and manufacturing.
Working closely with the Quality department to ensure compliance with cGMP, ICH, and FDA regulations.
Serving as an organizational change agent and fostering an atmosphere of a questioning attitude, empowerment, and an error prevention/continuous improvement mindset.
Required Skills
A minimum of 1 year experience in adherent cell culture.
Deeper understanding of cell culture and ability to troubleshoot common processing issues.
Exceptional communication and interpersonal skills.
Ability to collect and assist in the analysis/trending of data and information to determine paths for process improvement and potential root cause.
Demonstrates technical proficiency, scientific creativity, problem-solving skills, strong GMP principles, and collaboration with others.
Must have full working knowledge of cGMP regulations.
Ability to work in a dynamic environment, multi-task, and meet aggressive deadlines.
Demonstrated critical thinking and problem-solving skills.
Ability to work independently, as well as work on larger cross-department projects as a team.
Application Deadline:
2024-09-16
#J-18808-Ljbffr
MSAT Associate II, Materials Science and Technology
Job Number:
83464
Location:
San Diego, US
Salary:
$75-95K
Job Description:
We are seeking a motivated, science-oriented individual with proficient knowledge of GMP manufacturing and an understanding of cell culture/cell therapies.
Responsibilities
The Materials Science and Technologies (MSAT) Associate II will need to learn/train quickly to provide Subject Matter Expert (SME) feedback for the various manufacturing processes.
This position will support CMC operations focusing on process development/optimization, technology transfers, change controls, manufacturing operations, and creation or revision of controlled documents.
Providing support to the MSAT Team and working cross-functionally to ensure clear communication across various departments.
Training on the cell therapy platforms quickly to assist in compiling scientific data relating to the cell therapy and new platforms.
Assisting with all tech transfers into cGMP Manufacturing, ensuring the transfer is controlled and executed within GMP regulatory guidelines.
Supporting the Manufacturing group and troubleshooting production activities to ensure safe, quality, and timely manufacture of biopharmaceutical products for pre-clinical, clinical, and commercial use.
Creating or revising (as needed) and reviewing all process-related manufacturing documentation (batch records, SOPs, bills of material, tech transfer documents, risk assessments, and process flow diagrams) to assure all clinical products meet the requirements for quality, safety, and efficacy.
Performing manufacturing deviation investigations to help determine root cause and product impact.
Providing in-person and real-time manufacturing production support as needed.
Identifying process improvement opportunities and/or corrective actions to increase yield, maximize capacity, improve operational efficiency, reduce costs, and ensure safety while maintaining regulatory compliance in collaboration with Research and Product Development and manufacturing.
Working closely with the Quality department to ensure compliance with cGMP, ICH, and FDA regulations.
Serving as an organizational change agent and fostering an atmosphere of a questioning attitude, empowerment, and an error prevention/continuous improvement mindset.
Required Skills
A minimum of 1 year experience in adherent cell culture.
Deeper understanding of cell culture and ability to troubleshoot common processing issues.
Exceptional communication and interpersonal skills.
Ability to collect and assist in the analysis/trending of data and information to determine paths for process improvement and potential root cause.
Demonstrates technical proficiency, scientific creativity, problem-solving skills, strong GMP principles, and collaboration with others.
Must have full working knowledge of cGMP regulations.
Ability to work in a dynamic environment, multi-task, and meet aggressive deadlines.
Demonstrated critical thinking and problem-solving skills.
Ability to work independently, as well as work on larger cross-department projects as a team.
Application Deadline:
2024-09-16
#J-18808-Ljbffr