Validation Engineer

• Posted 4 hours ago • Updated 4 hours ago
Full Time
On-site
USD $39.00 - 42.00 per hour
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Medical Devices
  • Pharmaceutics
  • FOCUS
  • Risk Assessment
  • Collaboration
  • Process Optimization
  • Continuous Improvement
  • Regulatory Compliance
  • ISO 9000
  • Training
  • Manufacturing
  • Documentation
  • Accessibility
  • Auditing
  • Management
  • Life Sciences
  • Technical Writing
  • Analytical Skill
  • Conflict Resolution
  • Problem Solving
  • Good Manufacturing Practice

Summary

Validation Engineer Job Opening

Validation Engineer

We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity.

Location: On-site
Focus: Process Validation
Pay Range: $39/hr - $42/hr (depending on experience)

Responsibilities
  • Develop, write, review, and execute process validation/process verification protocols and reports.
  • Conduct risk assessments and develop validation strategies for new and existing processes.
  • Analyze and interpret process validation data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.
  • Collaborate with Manufacturing, Quality, Design Transfer Operations, and other departments to resolve validation issues and implement corrective actions.
  • Participate in process optimization and continuous improvement initiatives to enhance quality and efficiency.
  • Ensure compliance with FDA, ISO, and other relevant regulatory guidelines, as well as adherence to internal requirements.
  • Provide training and guidance to manufacturing and quality personnel on validation processes and procedures.
  • Maintain process validation documentation and ensure traceability and accessibility for audits and inspections.
  • Perform other duties as assigned by management.


Qualifications
  • Bachelor's Degree in Engineering or Life Science.
  • Strong technical writing, analytical, and problem-solving skills.
  • Knowledge of cGMP and regulatory standards.
  • Strong understanding of process validation principles, techniques, and industry standards.
  • #LI-MB1


Equal Opportunity Employer
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: sharpdec
  • Position Id: 52739
  • Posted 4 hours ago
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