Brillfy Technology
Brillfy Technology

Quality Engineer (GMP/Pharma Manufacturing)

Phillipsburg, NJ, US • Posted 2 hours ago • Updated 2 hours ago
Contract W2
Contract Independent
12 Months
No Travel Required
On-site
$40/hr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Analytical Skill
  • Auditing
  • Biotechnology
  • Collaboration
  • Chemistry
  • Communication
  • Corrective And Preventive Action
  • GDP
  • GMP
  • Good Manufacturing Practice
  • Management
  • ISO 9000
  • Manufacturing
  • Pharmaceutics
  • Quality Assurance
  • Quality Management
  • Regulatory Compliance
  • Science
  • Statistical Process Control
  • Training
  • cGMP

Summary

Role: GMP Quality Assurance Engineer / Quality Systems Engineer
Location: Phillipsburg, NJ (Onsite M-F)
Duration: 18 Months Contract-to-Hire
Client: Avantor
Interview Process: 15-min Teams + 2-hour onsite interview

 

Job Description:

The ideal candidate will have experience in pharmaceutical, biotech, or chemical manufacturing environments and strong knowledge of cGMP and ISO standards.

 

Required Skills:

  • 5+ years of Quality Engineering / Quality Assurance experience
  • Experience in pharmaceutical, biotechnology, chemical, or GMP manufacturing environments
  • Strong knowledge of cGMP, ISO 9000, FDA regulations, CAPA, audits, validation
  • Experience handling customer complaints and investigations
  • Background in Quality Systems and compliance programs
  • Bachelor’s degree in chemistry or related Science field
  • Excellent communication and analytical skills

 

Preferred Skills:

  • Experience with ICHQ7, IPEC guidelines
  • Stability, SPC, validation experience
  • Internal/supplier audit experience
  • GMP/GDP training experience

Responsibilities:

  • Lead quality assurance and compliance programs
  • Manage CAPA and complaint investigations
  • Support GMP, ISO, regulatory, customer, and internal audits
  • Perform validation and statistical evaluations
  • Drive quality improvements and corrective actions
  • Collaborate with operations, suppliers, and customers
  • Ensure ongoing compliance with FDA and ISO standards

Work Environment:

  • Manufacturing facility environment
  • PPE required in designated areas
  • Occasional domestic travel
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: 91134346
  • Position Id: 8971020
  • Posted 2 hours ago
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