katalyst jobs in Los Angeles

Job-ID Reference Responsibilities: The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs...

Katalyst CRO is seeking a Quality Specialist with experience in Healthcare, Pharmaceutical, Medical Device, or Regulated Distribution to support QMS operations, supplier quality programs, and regulatory compliance activities. The ideal candidate will understand FDA 21 CFR Part 211, ISO 13485, supplier quality processes, and document-controlled QMS...

Katalyst CRO is seeking a Quality Specialist with experience in Healthcare, Pharmaceutical, Medical Device, or Regulated Distribution to support QMS operations, supplier quality programs, and regulatory compliance activities.The ideal candidate will understand FDA 21 CFR Part 211, ISO 13485, supplier quality processes, and document-controlled QMS...

Job Description Quality Specialist with experience in Healthcare, Pharmaceutical, Medical Device, or Regulated Distribution environments to support Quality Management System (QMS) operations, supplier quality programs, quality agreements, SOP development, and regulatory compliance activities. The ideal candidate will have strong knowledge of FDA 21 CFR Part...

Katalyst CRO is seeking a Delivery Assurance Specialist to drive supplier performance across the aerospace/defense supply chain. This role focuses on on-time delivery, supplier development, and quality improvement through ERP systems, Lean/Six Sigma, and cross-functional collaboration. You will monitor compliance, validate recovery plans, and lead supplier...

Job Description We are seeking a highly skilled and proactive Delivery Assurance Specialist to support and drive supplier performance within the aerospace and defense supply chain. This role is critical in ensuring on-time delivery, supplier development, and quality improvement across a complex supplier network. The ideal candidate will have a strong...

Katalyst CRO is seeking a hands-on Supplier Quality Engineer to own supplier qualification, approval, and lifecycle management for medical device components. You will manage ASLs, conduct supplier audits, and drive PPAP submissions in a regulated setting. The role requires IQ/OQ/PQ process validation understanding, risk-based decision making per ISO 14971,...

Job Summary Supplier Quality Engineer role requiring strong hands-on experience in supplier qualification, approval, and lifecycle management. The candidate should have proven capability in managing Approved Supplier Lists (ASL), conducting supplier audits, and handling PPAP submissions for medical device components. Requires solid understanding of process...

Job Description: Quality Specialist with experience in Healthcare, Pharmaceutical, Medical Device, or Regulated Distribution environments to support Quality Management System (QMS) operations, supplier quality programs, quality agreements, SOP development, and regulatory compliance activities. The ideal candidate will have strong knowledge of FDA 21 CFR...

Job Description: This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area. This role will be supporting validation leads to help ensure the required deliverables and testing are complete according to the Client CSV SOP. Effective...

Job Description: Identify and document defects on the shop floor and trace similar issues in previously built units. Collect, analyze, and communicate non-conformance data effectively. Perform root cause analysis and investigate quality issues using structured problem-solving techniques. Collaborate with cross-functional teams to ensure timely...

Job Description: Support the deployment of the MTO aspiration "to innovate to safely supply quality products and services competitively, faster, always". Responsible for providing advanced engineering design and start-up of GMP large molecule biologics manufacturing facility systems, and equipment. Provide integrated equipment, utility, and facility...

Responsibilities: The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs Develop and...

Katalyst CRO is seeking a Sr. Statistical Programmer in Los Angeles to support biostatistics with analysis datasets, tables, listings, and figures for regulatory submissions and publications.The role emphasizes SDTM/ADaM standardization, development of templates/macros, and collaboration with cross-functional teams to ensure timely, high-quality deliverables...

Job SummaryWe are seeking a Supplier Quality Engineer to support supplier quality management, incoming material quality, nonconformance investigations, risk assessment, and continuous improvement activities. The role will work closely with Quality, Operations, Engineering, and external suppliers to identify and resolve quality issues, improve supplier...

Job Description:The Senior Manufacturing Engineer serves as the technical process owner responsible for manufacturing process validations, performance, equipment readiness, capacity expansion, and continuous improvement activities to meet the yield, capacity, throughput, reliability, and quality goals. This role drives the development, validation,...

Job SummaryWe are seeking a Supplier Quality Engineer to support supplier quality management, incoming material quality, nonconformance investigations, risk assessment, and continuous improvement activities. The role will work closely with Quality, Operations, Engineering, and external suppliers to identify and resolve quality issues, improve supplier...

Job DescriptionThe Senior Manufacturing Engineer serves as the technical process owner responsible for manufacturing process validations, performance, equipment readiness, capacity expansion, and continuous improvement activities to meet the yield, capacity, throughput, reliability, and quality goals. This role drives the development, validation,...

Katalyst CRO in Los Angeles seeks an experienced CSV professional to lead validation activities for enterprise GxP systems. You will support validation leads, ensure deliverables, and drive testing in a fast-paced project environment.The role requires strong writing skills, regulatory knowledge (FDA/ICH), and ability to leverage AI tools to accelerate...

Job Description This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area. This role will be supporting validation leads to help ensure the required deliverables and testing are complete according to the Client CSV SOP. Effective...