Highlight
Summary
About the Role
About You
- 1-3 years of experience in GMP (manufacturing, QC, or QA).
- Bachelor's degree in a scientific field or data-heavy background (e.g., biology, chemistry, physics, computer science, accounting mathematics).
- Proficiency in Microsoft Excel and Word.
- Experience with MES, LIMS, SharePoint, and ERP platforms.
- Understanding of data integrity review regarding GMP expectations.
- Ability to collaborate in a team and work independently.
Benefits
- Competitive hourly wage of $30-32.
- Opportunity to work in the pharmaceutical manufacturing industry.
Tech Observer has been providing Staffing(Clinical/Scientific/IT/Professional) and Clinical Research Services since 2005. We have offices in New Jersey: US (Headquarters), India ,UK, Denmark and Singapore. Being ISO 9001:2008, ISO 14155:2011 and ISO 27001 certified company, we believe in quality & responsible work ethic. We are proud in providing strategic & real-time insights to the client to achieve their goals. Our services range offer flexible solutions to our clients ranging from ‘standalone service’ to ‘end to end support’ for their needs. With a team of 500 employees globally, we are serving more than 50 companies in over 30 countries. Our Key Services are: • Clinical Operations • Clinical Data Management • Biostatistics & SAS Programming • Medical Writing & Scientific Communications • Post-Marketing Clinical Studies • Staffing (US only) For more details visit us at www.tech-observer.com