The Role
Support biotechnology/pharmaceutical drug substance processes and GMP manufacturing systems. Provide process engineering support, technical writing, and use SAP, TrackWise, PAS/X, and Veeva. Bilingual Spanish/English required.
Summary Generated by Built In
Sr Engineer with experience in biotechnology pharmaceutical process support, especially on Drug Substance processes,
and GMP pharmaceutical manufacturing systems. Knowledge in SAP, TrackWise, electronic batch records (PAS/X) , and documents management systems (Veeva).
Requirements
- Doctorate or Masters + 2 years of Engineering experience or
Bachelors in Engineering + 4years of Engineering experience
Bilingual (Spanish/English)(Write/Speak)
Technical Writing
Skills Required
- Doctorate or Masters plus 2 years engineering experience, or Bachelors plus 4 years engineering experience
- Experience in biotechnology/pharmaceutical process support, especially Drug Substance processes
- Knowledge of GMP pharmaceutical manufacturing systems
- Experience with SAP
- Experience with TrackWise
- Experience with electronic batch records (PAS/X)
- Experience with document management systems (Veeva)
- Bilingual Spanish/English (written and spoken)
- Technical writing skills
Am I A Good Fit?
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.
Success! Refresh the page to see how your skills align with this role.
The Company
What We Do
QRC Group specializes in providing expert consulting services in regulatory compliance, quality management, and risk management for the pharmaceuticals, medical devices, biotechnology, and other regulated industries, delivering comprehensive project management and validation solutions.
