Katalyst
Katalyst

60 Katalyst Validation Engineer Jobs Hiring in CA

Quality Engineer

Pleasanton, CA

$80K - $103K/yr

Summary We are looking for a Quality Engineer with 0-3 years of experience to support quality systems, validation, CAPA, and compliance activities in a regulated medical device/pharma environment.

Quality Engineer

Santa Clarita, CA · On-site

$73K - $95K/yr

Evaluate test method validations, test fixture qualifications, and regression analysis. * Support ... Requirements: * Medical Device Quality Engineering. * Design Verification & Validation (DV&V)

Define, develop, and validate/transfer test methods. * Create verification plans, protocols ... A degree in an engineering field (mechanical, materials, packaging, bioengineering): BS or ...

Review and approve validation protocols and reports including IQ, OQ, PQ, TMV, and process ... Review engineering changes and assess quality and regulatory impacts. * Present quality performance ...

Quality Engineer with experience in the Medical Device industry, specializing in quality engineering, design assurance, risk management, design controls, and product verification & validation. Strong ...

Develop and validate control systems for precise XYZ multi axis mechanical motion, motion profiling, and closed-loop feedback systems. * Collaborate with mechanical engineers to define and validate ...

Senior Quality Engineer

San Diego, CA · On-site

$94K - $127K/yr

The role works cross-functionally to support design verification, process validation, and commercialization activities. Roles & Responsibilities: * Perform Quality Engineering activities related to ...

Instrumentation Quality Engineer

Lake Forest, CA · On-site

$76K - $98K/yr

... quality engineering support across the product development lifecycle. You will contribute to key ... validation, supplier-related quality support, change control, and product transfer. The ideal ...

Sr Quality Engineer

Irvine, CA · On-site

$94K - $127K/yr

Develop and execute test method validations and qualification plans * Support design verification ... Bachelor's degree in Engineering or Scientific field & 4+ years' experience OR Master's degree or ...

Our client is looking for an experienced and well-rounded CSV (Computer System Validation ... Supporting data migration initiatives as a CSV Engineer * Ensuring compliance with validation and ...

Manufacturing Engineer

Pleasanton, CA · On-site

$82K - $105K/yr

Experienced in manufacturing operations, process validation (IQ/OQ/PQ), configuration management ... Supported manufacturing engineering activities in a regulated medical device manufacturing ...

They are currently seeking a Senior Design Quality Engineer to support design quality integration ... Verification & Validation (V&V) * Change Controls * Root Cause Analysis / CAPA support * Process ...

Senior R&D Project Engineer

Irvine, CA · On-site

$105K - $136K/yr

Support process validation, risk assessments, and product change control activities. * Review and finalize validation documentation, risk management files, and regulatory documentation. * Manage ...

Senior R&D Project Engineer

Irvine, CA

$105K - $137K/yr

Support process validation, risk assessments, and product change control activities. * Review and finalize validation documentation, risk management files, and regulatory documentation. * Manage ...

Sr. Quality Engineer

Santa Clara, CA

$103K - $140K/yr

This role supports product development, manufacturing, validation, and quality assurance activities ... Collaborate with Engineering, Manufacturing, Operations, and Quality teams to resolve product and ...

Support design verification and validation activities. * Collaborate across engineering and cross-functional teams to meet project objectives. * Provide technical leadership and influence ...

Quality Engineer

Irvine, CA

$76K - $98K/yr

Support development and execution of relevant process development and validation activities (e.g ... A minimum of a bachelor's degree required (preferably in Engineering or related technical field ...

Proficient in test method analysis and test method validation * Good documentation skills with ... Bachelor's degree in mechanical engineering, biomedical engineering, or a related field. * 5+ years ...

Ensure Design Verification & Validation (V&V) activities meet requirements. * Review and approve, Engineering Change requests/Orders (ECR/ECOs). * Ensure design changes follow proper change control ...

Showing results 21-40

Katalyst Jobs Information

What is it like to work at Katalyst?

Katalyst appears to be a collaborative and innovative company that values creativity and teamwork, fostering an environment where employees can share ideas and work together to achieve common goals.

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.

What makes Katalyst an attractive place to work?

Katalyst is a forward-thinking company that has established itself as a leader in its industry, known for its commitment to innovation and customer satisfaction. The company's work environment is characterized by a collaborative and dynamic atmosphere, where employees are encouraged to share ideas and work together to drive progress. Joining Katalyst offers opportunities for professional growth and development, as well as the chance to contribute to meaningful projects that can have a lasting impact.

What are the most popular jobs at Katalyst in California?

Infographic showing various Validation Engineer job openings at Katalyst in California as of August 2026, with employment types broken down into 97% Full Time, and 3% Nights. Highlights an 97% Physical, and 3% Remote job distribution.

$80K - $103K/yr

Full-time

Re-posted 6 days ago


Job description

Summary
We are looking for a Quality Engineer with 0–3 years of experience to support quality systems, validation, CAPA, and compliance activities in a regulated medical device/pharma environment. The role involves working closely with cross-functional teams to ensure product quality and regulatory compliance.
Roles & Responsibilities:
  • Support equipment, process, and software validation (CSV, IQ/OQ/PQ).
  • Assist with CAPA, non-conformance (Client/MRB), and root cause investigations.
  • Maintain quality documentation and analyze quality metrics.
  • Support internal/external audits and ensure compliance with FDA, ISO 13485, and GMP requirements.
  • Collaborate with Engineering, Manufacturing, and R&D on quality initiatives.
Requirements:
  • Bachelor's degree in Engineering, Biomedical Engineering, or a related field.
  • 0–3 years of experience in Medical Devices, Pharma, Biotech, or other regulated manufacturing environments.
  • Basic knowledge of FDA 21 CFR 820, ISO 13485, CAPA, Validation, and Quality Management Systems.
  • Strong analytical, documentation, and communication skills.
  • Exposure to CSV, IQ/OQ/PQ, ISO 14971, GMP, or cleanroom environments.