Seeking a Senior CQV / Tech Transfer Engineer with 5+ years of experience in pharmaceutical, biotech, or biologics manufacturing. The role will support equipment qualification, validation, commissioning, technology transfer, and GMP manufacturing readiness.
Key Responsibilities
Support CQV, commissioning, qualification, and validation activities.
Author and execute IQ/OQ/PQ protocols and reports.
Support technology transfer, equipment startup, and operational readiness.
Develop/update URS, SOPs, and validation documentation.
Troubleshoot qualification issues and support investigations.
Collaborate with Engineering, Manufacturing, Quality, and Validation teams.
Requirements
Bachelor's degree in Engineering, Life Sciences, or related field.
5+ years of CQV, validation, equipment qualification, manufacturing engineering, or tech transfer experience.
Pharmaceutical, biotech, biologics, or sterile manufacturing experience.
Strong GMP experience.
Hands-on IQ/OQ/PQ protocol development and execution.
Experience with equipment qualification, commissioning, or technology transfer.
Strong technical writing and documentation skills.
Numbers & Facts
Location
NULL, IN
Salary
$55–$59
Skills
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Commissioningunmatched
Equipment Validationunmatched
GMP (Good Manufacturing Practices)unmatched
Identify Issuesunmatched
Manufacturingunmatched
Manufacturing Engineeringunmatched
Process Validationunmatched
Standard Operating Procedures (SOP)unmatched
System Start-Upunmatched
Technical Supportunmatched
Technical Writingunmatched
Validation Documentationunmatched
Writing Skillsunmatched
🎯
Be found by employers
5,500+ employers search our resume database daily. Add yours to get found by recruiters looking for candidates like you.
Level up your application
Professional resume templates
Browse dozens of recruiter approved resume templates, layouts and formats. Choose your favorite and make it your own in minutes.