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Wireless System Validation Engineer Jobs (NOW HIRING)

Apple

Wireless Systems Architect

San Jose, CA · On-site

$284K/yr

... wireless system validation. In this technical role, you'll be part of a product systems ... You'll work with talented RF HW, SW and design engineers in shaping wireless architecture, design ...

Apple

Wireless System Engineer

Cupertino, CA · On-site

We are looking for an expert wireless systems engineer who has deep understanding of wireless protocol interactions within the network, interactions across different layers of wireless protocols ...

Cypress HCM

Senior System Validation Engineer

San Jose, CA · Hybrid

$122K - $167K/yr

Senior System Validation Engineer This exciting role will be responsible for validating high-speed memory buffer semiconductor products, developing automation scripts, and ensuring system compliance ...

Apple

Wireless System Engineer

Cupertino, CA

$171K - $302K/yr

We are looking for an expert wireless systems engineer who has deep understanding of wireless protocol interactions within the network, interactions across different layers of wireless protocols ...

Apple

Wireless System Engineer

Cupertino, CA · On-site

We are looking for an expert wireless systems engineer who has deep understanding of wireless protocol interactions within the network, interactions across different layers of wireless protocols ...

Cypress HCM

Senior System Validation Engineer

Johns Creek, GA · Hybrid

$96K - $132K/yr

Senior System Validation Engineer This exciting role will be responsible for validating high-speed memory buffer semiconductor products, developing automation scripts, and ensuring system compliance ...

Apple

Wireless System Engineer

Cupertino, CA

$171K - $302K/yr

We are looking for an expert wireless systems engineer who has deep understanding of wireless protocol interactions within the network, interactions across different layers of wireless protocols ...

Apple

Wireless System Engineer

Cupertino, CA

$120K - $210K/yr

We are looking for an expert wireless systems engineer who has deep understanding of wireless protocol interactions within the network, interactions across different layers of wireless protocols ...

Apple

SerDes System Validation Engineer

Austin, TX

We have an opportunity for a forward-thinking and especially hardworking system validation engineer with strong background in high speed serial links. As a member of our dynamic team, you will have ...

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All JobsWireless System Validation Engineer Jobs

Wireless System Validation Engineer information

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How much do wireless system validation engineer jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for wireless system validation engineer in the United States is $51.80, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $64.42 per hour, depending on experience, location, and employer.
Infographic showing various Wireless System Validation Engineer job openings in the United States as of May 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $107,747 per year, or $51.8 per hour.
Computer System Validation Engineer

Computer System Validation Engineer

Katalyst HealthCares & Life Sciences

Princeton, NJ • On-site

Full-time

Posted 11 days ago

Job description

Csv Specialist

The CSV Specialist is responsible for planning, coordinating, and executing validation activities for computer systems to ensure compliance with regulatory requirements. This role involves working closely with IT, Quality Assurance, and business stakeholders to validate new and existing systems, document validation evidence, and support audits and inspections.

Roles & responsibility:

  • Knowledge on FDA Guidance's and industry Standards
  • Develop and execute validation plans, protocols (IQ/OQ/PQ), and reports for computer systems.
  • Assess and document system requirements, risk assessments, and user requirements specifications (URS).
  • Review and approve system design, configuration, and test documentation.
  • Ensure compliance with regulatory requirements (e.g., FDA 21 CFR Part 11, GAMP 5, EU Annex 11).
  • Manage change control and deviation management processes for validated systems.
  • Collaborate with cross-functional teams (IT, QA, business users) to ensure validation deliverables are met.
  • Maintain validation documentation and support periodic reviews and revalidation.
  • Participate in internal and external audits and respond to regulatory inquiries.
  • Train users and stakeholders on validated systems and compliance requirements.
  • Stay current with industry trends, regulations, and best practices in computer system validation.

Education & Experience:

  • Bachelor's degree in Computer Science, Life Sciences, Engineering, or related field.
  • 2+ years of experience in computer system validation or a regulated industry.
  • Knowledge of applicable regulations (FDA, EMA, GxP, 21 CFR Part 11, Annex 11).
  • Experience with validation methodologies (GAMP 5, risk-based validation).
  • Strong documentation, analytical, and problem-solving skills.
  • Excellent communication and teamwork abilities.
  • Experience with ERP, LIMS, MES, or other regulated systems is a plus
  • Familiarity with project management tools and methodologies
  • Experience with audit preparation and participation.
  • Understanding of data integrity principles.
  • Certification in validation or quality assurance (e.g., ASQ, ISPE) is a plus.
  • Prior work experience in Medical Device Industry, Biotechnology or Pharmaceutical industry is a plus.
Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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