You are successfully logged out of your my randstad account

You have successfully deleted your account

    Thank you for subscribing to your personalized job alerts.

    2 Temp to Perm Biotechnology & pharmaceutical found

    Filter2
    Clear all
      • Indianapolis, Indiana
      • Temp to Perm
      • $32.00 - $33.00 per hour
      Spherion is hiring Manufacturing Technicians in Indianapolis, IN.Fri-Sun 7am-7:30pm (must be able to train M-F 7am-3:30pm for the first few weeks)-Set-up and calibrate equipment for operation and testing to specification- May adjust filler and labeler equipment with proper parts and settings for products to be portioned-Assemble containers and components for portioning process. Assure they are correctResponsibilities:-Have demonstrated expertise in one or
      Spherion is hiring Manufacturing Technicians in Indianapolis, IN.Fri-Sun 7am-7:30pm (must be able to train M-F 7am-3:30pm for the first few weeks)-Set-up and calibrate equipment for operation and testing to specification- May adjust filler and labeler equipment with proper parts and settings for products to be portioned-Assemble containers and components for portioning process. Assure they are correctResponsibilities:-Have demonstrated expertise in one or
      • College Station, Texas
      • Temp to Perm
      • $20.00 per hour
      The Quality Assurance (QA) Associate is a vital role responsible for supporting and executing the site's Quality Management System (QMS). You will provide independent quality oversight of manufacturing, packaging, testing, and distribution to ensure all operations remain in a state of control and compliant with global regulatory standards, including 21 CFR Parts 210/211 and EU GMPsResponsibilities:Documentation & Compliance: Perform detailed reviews of bat
      The Quality Assurance (QA) Associate is a vital role responsible for supporting and executing the site's Quality Management System (QMS). You will provide independent quality oversight of manufacturing, packaging, testing, and distribution to ensure all operations remain in a state of control and compliant with global regulatory standards, including 21 CFR Parts 210/211 and EU GMPsResponsibilities:Documentation & Compliance: Perform detailed reviews of bat

    Thank you for subscribing to your personalized job alerts.

    It looks like you want to switch your language. This will reset your filters on your current job search.