Engineer Level 2
Raymond, OH · On-site
Requires a BS or MS in engineering. * All the skills and abilities of Engineer L1. * Additionally, must be proficient in technical writing and possess computer skills for scientific and technical ...

Raymond, OH · On-site
Requires a BS or MS in engineering. * All the skills and abilities of Engineer L1. * Additionally, must be proficient in technical writing and possess computer skills for scientific and technical ...
Raymond, OH · On-site
Requires a BS or MS in engineering. * All the skills and abilities of Engineer L1. * Additionally, must be proficient in technical writing and possess computer skills for scientific and technical ...
The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). * This role ...
The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). * This role ...
We are looking for an experienced Commissioning & Qualification (C&Q) Engineer to join our team in support of a major capital expansion project involving the installation of four new packaging lines.
We are looking for an experienced Commissioning & Qualification (C&Q) Engineer to join our team in support of a major capital expansion project involving the installation of four new packaging lines.
Raymond, OH · Hybrid
Qualification: * BS/MS in Mechanical Engineering.
Raymond, OH · Hybrid
Qualification: * BS/MS in Mechanical Engineering.
Raymond, OH · On-site
A Software Engineer who works within a development team to lead the development of infotainment software with a focus on headunit software, creating a top-class infotainment platform that applied to ...
Raymond, OH · On-site
A Software Engineer who works within a development team to lead the development of infotainment software with a focus on headunit software, creating a top-class infotainment platform that applied to ...
We are seeking an experienced Senior Validation Engineer / Senior CQV Engineer to support commissioning, qualification, and validation activities for equipment, systems, software, and manufacturing ...
We are seeking an experienced Senior Validation Engineer / Senior CQV Engineer to support commissioning, qualification, and validation activities for equipment, systems, software, and manufacturing ...
Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related technical discipline * 5+ years of experience in computerized system validation, quality, or validation engineering ...
Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related technical discipline * 5+ years of experience in computerized system validation, quality, or validation engineering ...
We are seeking a highly skilled Sr. Engineer - Process Development (CQV) to support automated and semi-automated combination product assembly, labeling, and packaging operations within a GMP Final ...
We are seeking a highly skilled Sr. Engineer - Process Development (CQV) to support automated and semi-automated combination product assembly, labeling, and packaging operations within a GMP Final ...
Delaware, OH · On-site
Perform engineering calculations with respect to strength of materials, speeds, horsepower, temperature, pressure, force, etc. as related to machine and tool designs. * Analyzes engineering drawings ...
Delaware, OH · On-site
Perform engineering calculations with respect to strength of materials, speeds, horsepower, temperature, pressure, force, etc. as related to machine and tool designs. * Analyzes engineering drawings ...
Bachelor's degree in Engineering, Life Sciences, Quality Management, or a related field (Master's preferred). * Minimum of 10+ years of experience in Quality Management within pharmaceutical, medical ...
Bachelor's degree in Engineering, Life Sciences, Quality Management, or a related field (Master's preferred). * Minimum of 10+ years of experience in Quality Management within pharmaceutical, medical ...
Columbus, OH · On-site
Summary: The Procurement Specialist is responsible for supporting sourcing activities, managing supplier relationships, and ensuring timely procurement of materials and services. This role works ...
Columbus, OH · On-site
Summary: The Procurement Specialist is responsible for supporting sourcing activities, managing supplier relationships, and ensuring timely procurement of materials and services. This role works ...
Required Qualifications : * Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every ...
Required Qualifications : * Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every ...
Katalyst CRO is seeking a Senior Clinical SAS Programmer who will represent the programming function in multi-disciplinary team meetings. The role involves developing CDISC-compliant datasets and ...
Katalyst CRO is seeking a Senior Clinical SAS Programmer who will represent the programming function in multi-disciplinary team meetings. The role involves developing CDISC-compliant datasets and ...
Newark, NJ · On-site
Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for ... Excellent skills in SAS programming and statistical reporting. * Knowledge of CDISC standards for ...
Newark, NJ · On-site
Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for ... Excellent skills in SAS programming and statistical reporting. * Knowledge of CDISC standards for ...
Lake Success, NY · On-site
Clinical SAS Programmer - Katalyst Healthcares and Life Sciences. Lake Success, NY. Responsibilities: * Provide statistical programming support for clinical trial data reporting under the general ...
Lake Success, NY · On-site
Clinical SAS Programmer - Katalyst Healthcares and Life Sciences. Lake Success, NY. Responsibilities: * Provide statistical programming support for clinical trial data reporting under the general ...
Contribute to the development and maintenance of SAS macro programs and departmental programming standards. * Participate in SOP and work instruction development, including program validation and ...
Contribute to the development and maintenance of SAS macro programs and departmental programming standards. * Participate in SOP and work instruction development, including program validation and ...
San Francisco, CA · On-site
Contribute to the development and maintenance of SAS macro programs and departmental programming standards. * Participate in SOP and work instruction development, including program validation and ...
San Francisco, CA · On-site
Contribute to the development and maintenance of SAS macro programs and departmental programming standards. * Participate in SOP and work instruction development, including program validation and ...
Develop, implement and maintain SAS programming standards. * Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as ...
Develop, implement and maintain SAS programming standards. * Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
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