Apply Now

Validation Engineer

Remote in Tucson, AZ, US • Posted 10 hours ago • Updated 10 hours ago

Full Time

On-site

Fitment

Dice Job Match Score™

⏳ Almost there, hang tight...

Job Details

Skills

IQ
OQ
PQ
Risk Assessment
Process Engineering
Process Optimization
Continuous Improvement
Regulatory Compliance
ISO 9000
Training
Documentation
Accessibility
Auditing
Management
Life Sciences
Technical Writing
Analytical Skill
Conflict Resolution
Problem Solving
Good Manufacturing Practice
Biotechnology
Manufacturing
Medical Devices
Pharmaceutics

Summary

Job Description:

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.
This is an on-site position that focuses on equipment validation.

Responsibilities:

Develops, prepares, and executes IQ, OQ, and PQ protocols and reports for equipment/systems.
Conducts risk assessments and develops qualification strategies for new and existing equipment/systems.
Analyzes and interprets qualification data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.
Collaborates with cross-functional teams, including Process Engineering, Automation Maintenance Support, Design Transfer Operations, Manufacturing, Quality, Facilities, and Safety Health and Environment (SHE), to ensure seamless execution of qualification activities and successful achievement of qualification-related project milestones.
Participates in process optimization and continuous improvement initiatives to enhance quality and efficiency.
Ensures compliance with FDA, ISO, and other relevant regulatory guidelines, as well as adherence to internal requirements.
Provides training and guidance to manufacturing and quality personnel on qualification processes and procedures.
Maintains equipment/systems qualification documentation and ensures traceability and accessibility for audits and inspections.
Other duties as assigned by management.

Requirements:

Bachelor's degree in engineering or Life Science.
Strong technical writing, analytical, and problem-solving skills.
Knowledge of cGMP and regulatory standards.
Demonstrated experience assisting with or supporting qualification activities within the medical device, pharmaceutical, or biotechnology industry is required.
Experience: 1-3 years of experience in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA.)

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: 91116760
Position Id: b973ffac9c951b511db6326618fad5ec
Posted 10 hours ago

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

Validation Engineer

Remote or Tucson, Arizona

•

Today

Summary : We are seeking a proactive Validation Engineer with in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity. This is an on-site position that focuses on equipment validation. Roles & Responsibilities Develops, prepares, and executes IQ, OQ, and PQ protocols and reports for equipment/systems. Conducts risk assessments and develops qualification strategies for new and existing equipment/systems. n

Full-time

Validation Engineer

Oro Valley, Arizona

•

Today

Title: Validation Engineer Description: 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 This is an on-site position that focuses on equipment validation. Pay range for this position is $39/hr-$42/hr, depending on experience Experience: 1-3 years of experience in a regulated manufacturing environment (medical devices, pharm

Easy Apply

Contract

USD 39.00 - 42.00 per hour

Validation Engineer(Medical Device, FDA)

Tucson, Arizona

•

7d ago

Tittle ValidationEngineer Location- Tucson, AZ/Onsite Contract 12+ months Responsibilities Develops, prepares, and executes IQ, OQ, and PQ protocols and reports for equipment/systems.Conducts risk assessments and develops qualification strategies for new and existing equipment/systems.Analyzes and interprets qualification data, ensuring accuracy, completeness, and adherence to regulatory and internal requirements.Collaborates with cross-functional teams, including Process Engineering, Automatio

Easy Apply

Contract

Depends on Experience

Biomedical Validation Engineer

Tucson, Arizona

•

7d ago

Job Title: Validation Engineer Location: Tucson, AZ (Onsite) Position Overview We are seeking a Validation Engineer with 1 3 years of experience in a regulated manufacturing environment (medical device, pharmaceutical, or biotechnology industry) to support equipment qualification and validation activities. This is a hands-on onsite role focused on ensuring compliance, operational integrity, and successful execution of equipment qualification projects. Required Qualifications Bachelor's Degree in

Easy Apply

Contract

$30 - $42

Search all similar jobs

Remote jobs at Katalyst Healthcares and Lifesciences