Validation Engineer I (with exp in regulated manufacturing environment)

Overview

On Site
Depends on Experience
Contract - Independent
Contract - W2
Contract - 16 Month(s)

Skills

We are seeking a proactive Validation Engineer with 1-3 years of experience in a regulated manufacturing environment (medical devices or pharma (or) biotech preferably FDA)

Job Details

Tranzeal is an industry leading global Business Transformation Service Provider offering specific consulting services as well as prepackaged, industry specific solutions and services to companies around the world. Our Consulting Services are dedicated to helping our clients maximize their investments in IT and the overall effectiveness and efficiency of the business. Tranzeal s deep industry experience makes us the partner of choice for a growing number of Fortune 1000 companies, midsize enterprises and small businesses worldwide.

We are currently looking for 'Validation Engineer I (with exp in regulated manufacturing environment)' to support one of our clients with the following skills:

Requirement:

Job Title: Validation Engineer I (with exp in regulated manufacturing environment)
Location: Tucson, AZ
Duration: 16+ months
Pay Rate: doe

The validation engineer will focus on process validation vs. equipment qualification.

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 process validation.

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.
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.

 

 

The national base pay range below is a good-faith estimate of what our client may pay for new hires. Actual pay may vary based on Client's assessment of the candidates knowledge, skills, abilities (KSAs), related experience, education, certifications and ability to meet required minimum job qualifications. Other factors impacting pay include prevailing wages in the work location and internal equity. $70,000 - $84,000

 

 

 

 

 

 

 

 

 

Note: Please send your updated resumes to sureshs(at)tranzeal(dot)(com)

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.