
VALIDATION ENGINEERS
South Plainfield, NJFull-time$99K/yrSeen 1mo agoSeen in employer's feed 2 days ago
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Job overview
Premier Life Sciences seeks Validation Engineers to design, develop, and oversee validation components using tools such as AutoCAD, Python, and Matlab. The role involves writing engineering change orders, releasing aging reports, conducting risk‑based verification for GxP systems, and creating DFMEA for new implants and instruments. A Master’s degree in a relevant engineering field is required, and work will be on‑site in South Plainfield, NJ with occasional travel across the U.S.
Skills & qualifications
Skills
Qualifications
Full job description
Minimum Education Required
Master's degree
Compensation
$98,571.00 - $98,571.00 / Yearly
Hours Per Week
40
Number Of Positions
5
Shift
First Shift (Day)
Job Description
Design, develop and oversee validation components using AutoCAD, Python, Matlab, Kaizen, Minitab, Tally, Catia, Ansys and Gap Analysis. Write and execute engineering change orders related to Corrective and Preventive Actions (CAPA). Change in Critical to Quality (CTQs), release of aging reports and design history files. Conduct risk-based verification for GxP (GMP, GCP, and GLP) systems and laboratory equipment. Create, and update Failure Mode and Effect Analysis (DFMEA) for new implants and instruments. Master’s degree in Science, Technology, Engineering, Mechanical Engineering, Industrial Engineering, or Biotechnology Engineering (any) is required. Work location: South Plainfield, NJ and various unanticipated locations throughout the U.S.
Email Resume to HR Dept., Premier Life Sciences, LLC., at [email protected].
Place of Work
On-site
Requisition ID
VE709
Job Type
Full Time
Application Email
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