To be responsible for managing technology in projects and providing technical guidance or solutions for work completion. Regulated environment (Medica..Share
Conducts and manages resolution of deviations, root cause investigations, impact assessments and CAPAs as a Lead. Demonstrated basic project managemen..Share
CTD guidance and CDISC SDTM and ADaM standards) Assist in updating/writing PROMETRIKA standard operating procedures (SOPs) Develop tools in SAS for da..Share
Should have good understanding and experience on execution and managing GxP projects and deliverables. Worked in Life Sciences vertical both GxP and n..Share
Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards. Design validation approaches, s..Share
Call Center Rep Work From Home American Income Life (part of Globe Life, a NASDAQ traded company) is looking for Benefit Representatives to help manag..Share
Knowledge and working application of reading and understanding blueprints and technical drawings. Review individual complaints and associated service ..Share
Now accepting applicants for Focus Group studies. Earn up to $750 per week part-time working from home. Must register to see if you qualify. No call c..Share
Nice to have - experience working as a system administrator on Windows workstations/servers reviewing system logs, services, and settings with asset l..Share
Location: Concord, MA - Massachusetts Department of Corrections Schedule: Monday-Friday, 8:00am - 4:00pm. Possibility of one 11:00am-7:00pm shift and ..Share
Location: CHA Cambridge Hospital Work Days: 3 days per week Category: Medical Assistant Department: CHA Obstetrics & Gynecology Center Cambridge Job..Share
Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page! Job details Hunter Needed. Prefer candidates to be in..Share
Good understanding of Process Validation requirements and life science concept is a plus. List primary duties and responsibilities for this position i..Share
Provide technical expertise and support related to existing and new manufacturing processes and work directly with production staff to improve, mainta..Share
Solid understanding of federal and international medical device regulations, such as FDA QSR, ISO 14971,62304, and 13485, and EU MDR. In conjunction w..Share