Computer Systems Validation Engineer

R&D Partners

Redwood City (CA)

Hybrid

USD 135,000 - 166,000

Full time

5 days ago
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Benefits offered by this job

Medical insurance
401k plan
Employee Assistance Program
Long-term disability
Weekly payroll
Online timecard approval

Job summary

R&D Partners is hiring a Computer System Validation Engineer for a 12-month, on-site contract in Redwood City with a hybrid schedule. You will lead validation strategies, create comprehensive documentation, and perform risk assessments to ensure GMP/GxP compliance across ERP, LIMS, and MES systems.

Ideal candidates have 2–5 years in CSV, strong regulatory knowledge (FDA/EMA), and excellent writing skills. Collaboration with IT, QA, and Operations is essential for successful validations and

Qualifications

  • Bachelor's degree in Computer Science, Engineering, or a related field.
  • 2–5 years of experience in computer system validation or related field.
  • Strong knowledge of regulatory requirements (FDA, EMA) and standards (GAMP 5).
  • Experience validating ERP, LIMS, MES systems.

Responsibilities

  • Develop validation strategies for computer systems and software.
  • Create and maintain Validation Plans, Protocols (IQ/OQ/PQ), and Validation Reports.
  • Perform risk assessments to ensure compliance with regulatory requirements.
  • Collaborate with IT, QA, and Operations to validate systems.
  • Conduct validation testing and review results to meet requirements.
  • Provide training on validation processes to staff.
  • Participate in audits/inspections by regulatory agencies.

Skills

CSV engineering
Validation testing
Documentation
Regulatory knowledge
Independent worker

Education

Bachelor's degree in Computer Science or Engineering

Tools

IQ/OQ/PQ protocols

Job description

We are hiring a highly skilled Computer System Validation Engineer to join our team. The CSV Engineer will be responsible for ensuring that all computer systems and software used comply with regulatory requirements and industry standards. This role involves planning, executing, and documenting validation activities to ensure the integrity and reliability of these systems.

This is a 12-month contract onsite in Redwood City, California hybrid schedule.

Responsibilities
  • Develop and implement validation strategies for computer systems and software applications.
  • Create and maintain validation documentation, including Validation Plans, Protocols (IQ/OQ/PQ), and Validation Reports.
  • Perform risk assessments to identify potential issues and ensure compliance with regulatory requirements.
  • Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure successful validation of systems.
  • Conduct validation testing and review test results to ensure systems meet specified requirements.
  • Provide training and support to staff on validation processes and procedures.
  • Stay up-to-date with industry trends and regulatory changes to ensure ongoing compliance.
  • Participate in audits and inspections by regulatory agencies.
  • Execute Validation Project Plans (VPPs) for manufacturing GxP systems such as, BMS, EMS, & PCS.
  • Support the execution of VPPs to qualify systems for GMP Manufacturing Equipment in accordance with Software Development Lifecycle (SDLC) procedures as per GAMP5 industry standards
  • Assist site Automation groups in configuring I/O and executing CSV protocol requirements.
  • Independently perform CSV lifecycle deliverables, including but not limited to, Functional Requirements Specification (FRS), Configuration Specification (CS), Electronic Records and Electronic Signatures (ERES), Risk Assessment (RA), Data Integrity (DI) Assessment, IQ/OQ/PQ, & Summary Report
Qualifications
  • Bachelor’s degree in Computer Science, Engineering, or a related field.
  • Minimum of 2-5 years of experience in computer system validation or a related field.
  • Strong knowledge of regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GAMP 5).
  • Experience with validation of various types of systems, including ERP, LIMS, and MES.
  • Excellent documentation and technical writing skills.
  • Strong analytical and problem-solving abilities.
  • Ability to work independently and as part of a team.
  • Excellent communication and interpersonal skills.
  • Preferred: Certification in Computer System Validation or related areas.
  • Experience with cloud-based systems and software validation, experience with Blue Mountain RAM.
  • $135,200-$166,400
Why Choose R&D Partners?

As an employee, you have access to a comprehensive benefits package including:

  • Medical insurance – PPO, HMO & HSA
  • 401k plan
  • Employee Assistance Program
  • Long-term disability
  • Weekly payroll
  • Online timecard approval

R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

R&D Partners is an equal-opportunity employer.

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