- ADM (Kennesaw, GA)
- …under cGMP/GLP environment as per company's standard operating procedures and USP/ FDA guidelines. + Assist Lab Administrator with scheduling analytical tests and/or ... equipment + Schedule and assist equipment repair technicians. + Assist Lab Manager with development of Capex requests. **Training and Proficiency** + Develop and… more
- Mentor Technical Group (Gurabo, PR)
- …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... Lead site audits. + Own site quality program procedures. + Designee for QA manager on local CCRB. + Review Risk Assessments. + Support Automation activities. +… more
- Fujifilm (Columbus, OH)
- …to cross sell additional products and options. + Work Hospital Relations Manager , National and Government Accounts to develop relationships and implement hospital ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Fujifilm (Macedonia, OH)
- …material neatly in designated area. + Order warehouse supplies through request to Manager of Warehouse. + Assist with the Physical Counts of Inventory: + Check ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Teva Pharmaceuticals (Edison, NJ)
- …Operators as required. * Perform additional duties as assigned by Supervisor or Manager . * Must be able to read, write, speak, and comprehend English. **Your ... or Equivalent Required Experience Required: * 1-2 years' experience in FDA regulated packaging environment desired. Specialized or Technical Knowledge, Licenses,… more
- Gilead Sciences, Inc. (La Verne, CA)
- …and conducts final reviews prior to batch release approval by manager Supervises personnel including organizing and prioritizing daily tasks, performing training ... Proficiency in Microsoft Office applications. Must possess a strong knowledge of the FDA and cGMP standards as well as regulatory guidance documents. 6+ years of… more
- Cardinal Health (Louisville, KY)
- …(QAS) performs all quality review and approval/release decisions at an FDA -regulated drug manufacturing facility. The facility manufactures two sterile liquid ... metrics related products and processes as deemed necessary by the Regional Quality Manager RQM. + Ensures the site manufactures products to meet the requirements of… more
- Insight Global (Florham Park, NJ)
- …to project teams and departments, and serving as a backup for the QA Manager . We are a company committed to creating diverse and inclusive environments where people ... R&D or Analytical in a GMP facility -Experience and understanding of FDA OTC Drug Listing Process -Experience and understanding GMP Procedures -Experience with… more
- Fresenius Medical Center (Lawrence, MA)
- …for assistance with complex problems that may arise. + Escalate issues to supervisor/ manager as necessary. + Review and comply with the Code of Business Conduct ... with proficiency in Microsoft Office applications. + Understand and apply FDA Guidelines, standards (ISO/AAMI/USP), and Design/Pharma Control Concepts. + Strong oral… more
- Nestle (Burlington, WI)
- …processes for compliance with quality and GMP requirements in accordance with FDA and OSHA regulations. + Provide construction management and plant startup ... assigned projects from end to end with minimal supervision from department manager . _Administrative / Business support- 15%_ + Provide technical support to Factory… more
Recent Jobs
-
Plastics Engineering Internship- Summer
- DEKA Research & Development (Manchester, NH)
-
Senior Manager, Information Records Governance
- Sumitomo Pharma (Oklahoma City, OK)
-
Expert DevOps Engineer
- SAP (Reston, VA)
-
Principal Software Developer
- Oracle (Pleasanton, CA)