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Katalyst Jobs in Texas (NOW HIRING)

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Katalyst information

What is a Katalyst?

A Katalyst job typically refers to a role focused on driving change, innovation, or transformation within a company or industry. It may involve leadership, strategy development, and process optimization to improve efficiency and growth. Responsibilities can vary by organization but often include problem-solving, collaboration, and implementing new initiatives. The role is suited for individuals who excel at adapting to challenges and inspiring progress.

What are the typical responsibilities of a Katalyst on a daily basis?

As a Katalyst, your daily activities often include facilitating team meetings, monitoring project progress, identifying improvement opportunities, and communicating with stakeholders to align goals. You might also be responsible for implementing new processes, training team members, and resolving workflow bottlenecks to ensure smooth operations. Depending on the organization, you'll work closely with cross-functional teams to drive innovation and productivity. This dynamic role requires adaptability and proactive problem-solving to help teams reach their full potential.

What are the key skills and qualifications needed to thrive in the Katalyst position, and why are they important?

To thrive as a Katalyst, you need strong project management, strategic planning, and change management skills, usually backed by a bachelor’s degree in business or a related field. Familiarity with productivity tools like Microsoft Office Suite, collaboration platforms such as Slack or Asana, and process improvement certifications like Six Sigma can be highly beneficial. Exceptional communication, problem-solving, and leadership abilities help set top Katalysts apart. These skills are crucial because Katalysts are often responsible for driving organizational transformation and ensuring teams achieve shared objectives efficiently.

What cities in Texas are hiring for Katalyst jobs?

Cities in Texas with the most Katalyst job openings:

Infographic showing various Katalyst job openings in Texas as of August 2026, with employment types broken down into 97% Full Time, 2% Part Time, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

$103K - $142K/yr

Other

This job post has expired today. Applications are no longer accepted.


Job description

Job Description:
The Senior Computer System Validation (CSV) Engineer is responsible for leading validation activities for computerized systems used in regulated environments such as pharmaceutical, biotechnology, or medical device manufacturing. This role ensures that systems including LIMS, ERP, MES, and laboratory applications are validated in compliance with FDA, EU, and global regulatory requirements. The Senior CSV Engineer will act as a subject matter expert (SME), providing guidance on validation strategy, risk-based approaches, and regulatory compliance across the system lifecycle.
Responsibilities:
  • Lead and execute computer system validation (CSV) activities for GxP-regulated systems.
  • Develop and review validation deliverables including validation plans, URS, FS, DS, risk assessments, IQ/OQ/PQ protocols, and summary reports.
  • Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and GxP regulations.
  • Define and implement risk-based validation strategies for computerized systems.
  • Oversee validation of systems such as LIMS, ELN, MES, ERP, CDS, and laboratory systems.
  • Support system implementations, upgrades, and decommissioning activities from a validation perspective.
  • Collaborate with IT, QA, Engineering, and business stakeholders to ensure compliant system deployment.
  • Lead change control assessments and determine validation impact of system changes.
  • Ensure data integrity (ALCOA+) compliance across validated systems.
  • Support audits and regulatory inspections by providing validation documentation and system justification.
  • Mentor and guide junior CSV engineers and validation team members.
  • Drive continuous improvement of validation processes, templates, and standards.
  • Review vendor documentation and ensure systems meet regulatory expectations prior to deployment.
Requirements:
  • Bachelor's degree in Engineering, Computer Science, Life Sciences, or related field.
  • 5-10+ years of experience in Computer System Validation (CSV) or validation engineering.
  • Strong experience in GxP-regulated pharmaceutical, biotech, or medical device environments.
  • Hands-on experience with validation of LIMS, MES, ERP, or laboratory systems.
  • Strong knowledge of 21 CFR Part 11, EU Annex 11, and GAMP 5 guidelines.
  • Experience authoring and executing IQ/OQ/PQ protocols and validation documentation.
  • Strong understanding of risk-based validation and data integrity principles.
  • Experience supporting regulatory audits and inspections.
Preferred Skills:
  • Experience with systems such as LabWare, SAP, Oracle, Veeva, TrackWise, Empower.
  • Knowledge of cloud-based validation and SaaS systems.
  • Experience in data integrity remediation projects.
  • Strong technical writing and documentation skills.
  • bility to lead cross-functional validation projects.
Key Competencies:
  • Strong leadership and SME-level expertise in CSV.
  • Excellent analytical and risk assessment skills.
  • Strong communication and stakeholder management.
  • bility to manage multiple validation projects simultaneously.
  • High attention to detail and regulatory compliance mindset.