Roles & Responsibilities: * Demonstrated experience working under Design Controls and ISO 13485 / FDA QSR environments. * Proven ability to conduct root cause analysis and support field driven ...

55 Katalyst Jobs Hiring in Texas
Roles & Responsibilities: * Demonstrated experience working under Design Controls and ISO 13485 / FDA QSR environments. * Proven ability to conduct root cause analysis and support field driven ...
Requirements: * Associate degree in Computer-Aided Drafting or equivalent * 4+ years of drafting/design experience in the structural field * 2+ years Revit experience * Experience designing ...
Requirements: * Associate degree in Computer-Aided Drafting or equivalent * 4+ years of drafting/design experience in the structural field * 2+ years Revit experience * Experience designing ...
Onsite Interface Manager
Houston, TX · On-site
Client & Project Coordination: * Serve as primary onsite interface with client engineering, operations, construction, and project management teams. * Participate in daily, weekly, and milestone ...
Onsite Interface Manager
Houston, TX · On-site
Client & Project Coordination: * Serve as primary onsite interface with client engineering, operations, construction, and project management teams. * Participate in daily, weekly, and milestone ...
Manufacturing Engineer
Fort Worth, TX · On-site
$69K - $90K/yr
Responsibilities: * Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. * Designs arrangement of ...
Manufacturing Engineer
Fort Worth, TX · On-site
$69K - $90K/yr
Responsibilities: * Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. * Designs arrangement of ...
Core Technician I
$18.50 - $23.25/hr
The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be ...
Core Technician I
$18.50 - $23.25/hr
The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be ...
Core Technician I
Houston, TX · On-site
$18.50 - $23.25/hr
The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be ...
Core Technician I
Houston, TX · On-site
$18.50 - $23.25/hr
The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be ...
Supports GMP manufacturing by performing environmental monitoring, cleanroom setup, aseptic tasks, and basic lab activities. Responsibilities: * Perform Environmental Monitoring in GMP cleanrooms ...
Supports GMP manufacturing by performing environmental monitoring, cleanroom setup, aseptic tasks, and basic lab activities. Responsibilities: * Perform Environmental Monitoring in GMP cleanrooms ...
Regulatory Affairs Manager
Addison, TX · On-site
Responsibilities: * This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems * This new team member will apply advanced regulatory ...
Regulatory Affairs Manager
Addison, TX · On-site
Responsibilities: * This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems * This new team member will apply advanced regulatory ...
Material Handler II
Houston, TX · On-site
$15.50 - $19/hr
The Material Handler supports Production and Supply Chain operations by managing material flow, performing SAP transactions, and maintaining inventory accuracy in a cGMPregulated pharmaceutical ...
Material Handler II
Houston, TX · On-site
$15.50 - $19/hr
The Material Handler supports Production and Supply Chain operations by managing material flow, performing SAP transactions, and maintaining inventory accuracy in a cGMPregulated pharmaceutical ...
Manufacturing Process Engineer
$68K - $91K/yr
Job Summary: * Manufacturing Process Engineer with experience in medical device manufacturing, responsible for developing manufacturing processes, performing validations, and ensuring compliance with ...
Manufacturing Process Engineer
$68K - $91K/yr
Job Summary: * Manufacturing Process Engineer with experience in medical device manufacturing, responsible for developing manufacturing processes, performing validations, and ensuring compliance with ...
This position functions as the technical and quality systems leader within QC Operations Support. Responsibilities: * Perform Compendial Assessments. * Author and Review Technical Documents. * Design ...
This position functions as the technical and quality systems leader within QC Operations Support. Responsibilities: * Perform Compendial Assessments. * Author and Review Technical Documents. * Design ...
Clinical Data Coordinator
Dallas, TX · On-site
Responsibilities: * Assist in the development, testing, and validation of Electronic Data Capture (EDC) systems and Case Report Forms (CRFs) * Support database setup activities including edit check ...
Clinical Data Coordinator
Dallas, TX · On-site
Responsibilities: * Assist in the development, testing, and validation of Electronic Data Capture (EDC) systems and Case Report Forms (CRFs) * Support database setup activities including edit check ...
Job Summary: * We are seeking a Verification & Validation (V&V) Engineer (Mechanical) to support Medical Device product development activities. * The role involves working with cross-functional teams ...
Job Summary: * We are seeking a Verification & Validation (V&V) Engineer (Mechanical) to support Medical Device product development activities. * The role involves working with cross-functional teams ...
Summary : We are looking for a Validation Engineer II with experience in the pharmaceutical or biopharmaceutical industry to join our growing team. Roles & Responsibilities: * Develop and execute IQ ...
Summary : We are looking for a Validation Engineer II with experience in the pharmaceutical or biopharmaceutical industry to join our growing team. Roles & Responsibilities: * Develop and execute IQ ...
Controls Systems Engineer - Power Generation
Houston, TX · On-site
$79K - $103K/yr
We are seeking a Controls Systems Engineer with hands on PLC programming experience to support the development, integration, and testing of industrial power generation control systems. This role ...
Controls Systems Engineer - Power Generation
Houston, TX · On-site
$79K - $103K/yr
We are seeking a Controls Systems Engineer with hands on PLC programming experience to support the development, integration, and testing of industrial power generation control systems. This role ...
Cleanroom Laboratory Technician
Houston, TX · On-site
$17.75 - $23.50/hr
We are seeking a Cleanroom Laboratory Technician to support manufacturing and laboratory operations within a regulated production environment. This position is responsible for environmental ...
Cleanroom Laboratory Technician
Houston, TX · On-site
$17.75 - $23.50/hr
We are seeking a Cleanroom Laboratory Technician to support manufacturing and laboratory operations within a regulated production environment. This position is responsible for environmental ...
Quality Control Tech 1
El Paso, TX · On-site
$15 - $19.25/hr
This position is responsible for efficient and effective performance of sampling raw materials and testing (except for the raw materials chemicals) in conformance with regulations and standards.
Quality Control Tech 1
El Paso, TX · On-site
$15 - $19.25/hr
This position is responsible for efficient and effective performance of sampling raw materials and testing (except for the raw materials chemicals) in conformance with regulations and standards.
Clinical Data Specialist
Austin, TX · On-site
Responsibilities: * Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing ...
Clinical Data Specialist
Austin, TX · On-site
Responsibilities: * Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing ...
Supplier Quality Engineer
San Antonio, TX · On-site
Job Summary: * The Supplier Quality SME provides technical and process leadership to enhance supplier quality systems and standardize best practices across the supply base * Focuses on identifying ...
Supplier Quality Engineer
San Antonio, TX · On-site
Job Summary: * The Supplier Quality SME provides technical and process leadership to enhance supplier quality systems and standardize best practices across the supply base * Focuses on identifying ...
Responsibilities: * Lead and manage publishing activities for IND, NDA, ANDA, Amendments, Supplements, Responses, Annual Reports, Safety Reports, and Promotional Submissions. * Oversee submission ...
Responsibilities: * Lead and manage publishing activities for IND, NDA, ANDA, Amendments, Supplements, Responses, Annual Reports, Safety Reports, and Promotional Submissions. * Oversee submission ...
Katalyst Jobs Information
What is it like to work at Katalyst?
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
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Job description
- Demonstrated experience working under Design Controls and ISO 13485 / FDA QSR environments.
- Proven ability to conduct root cause analysis and support field driven corrective actions.
- Strong written and verbal communication skills, including the ability to translate clinical feedback into engineering actions.
- Ability to work independently, prioritize multiple issues, and lead crossfunctional technical efforts.
- Direct exposure to field action support, complaints investigations, or post market surveillance.
- Familiarity with human factors standards (IEC 62366), risk management (ISO 14971), and related FDA guidance.
- Experience working closely with clinicians, clinical engineers, or medical affairs teams.
- Bachelor's degree in engineering or related technical field (mechanical, biomedical, or equivalent).
- 5 to 6 years of medical device development experience, including sustaining or post market engineering surveillance.
- Experience with structural heart or transcatheter cardiovascular devices.
- Experience owning or supporting IFUs, user needs, or human factors engineering for Class III medical devices.