THE LARGEST COLLECTION OF QA/QC JOBS ON EARTH
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Description Monday-Friday 11 30pm-6am 16 60 plus 1 00 shift differential Retention Bonus - 1 00 00 PayoutBreakdown 500 at 60 days and an additional 500 at completion of 120..
Description Monday-Friday 10 30pm-6 00 am or 11 30 pm - 6 00am or Part Time only 16 60 plus 1 00 shift differential Retention Bonus - 1 00 00..
Our Purpose We work to connect and power an inclusive, digital economy that benefits everyone, everywhere by making transactions safe, simple, smart and accessible. Using secure data and networks, partnerships..
ABOUT US Arranta Bio is a rapidly growing and dynamic bio-pharmaceutical contract development and manufacturing organization (CDMO). Our vision is to be the best in class CDMO providing development and..
The RolennReporting to the Sr. Manager of Quality Control (Microbiology), the Quality Control Associate II will support microbiological testing for GMP QC raw materials, excipients, drug substance and finished product..
The Board of Registration in Medicine within the Department of Public Health is seeking qualified Registered Nurses to apply to this Quality Analyst position. The incumbent reviews safety and quality..
Job Title: Quality Assurance - Clinical I Work Location: Andover - MA Duration: 18 Months (Possibility of Extension) on W2 Job Description: start looking for some hands-on exp., industry exp.,..
Job Description Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Quality Disposition in our Lexington, MA office...
Overview nFM Global is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000-size companies with engineering-based risk management and property insurance solutions. FM..
Description This is a full-time position located in Framingham, MA in the Quality Systems & Compliance Department. This position is responsible for the development, improvement, and maintenance of CRISPR Quality..
Title: QA Associate II – III, Development and External Quality Assurance Reports To: Cara Kaufhold Contract resource General Description: This function is responsible for supporting daily production operations of the..
Laboratory Supervisor II','20000673','!*! Laboratory Supervisor II – Supervisor of the DELS/WES Organic Chemistry Mass Spectrometry Laboratory – Lawrence The Massachusetts Department of Environmental Protection (MassDEP) is the state agency responsible..
OverviewnWalsh is currently seeking a Quality Manager for our Water/Waste Water Divisionnin Boston, MA.nThe Quality Manager II is responsible for implementation, improvement andnexecution of the Quality management systems (QMS) and..
QC Analyst I Job description Overview GENERAL SUMMARY OF POSITION: The QC Analyst I – Central Receiving is responsible for ensuring that the analysis of in process and finished formulation..
PDS Tech is seeking candidates for a Supplier Quality Analyst position in Somerville, MA Job Summary : This Supplier Quality Management (SQM) Associate, with assistance and oversight from SQM team,..
Position: Warehouse Quality Inspector Job Description: What You Will Be Doing: Prepare product for assembly, kits and packages product Perform builds of low complexity products according to build plan; install..
Description Company Apply Job Description Join bluebird bio’s enthusiastic and collaborative Quality Assurance team to contribute to the overall success of our novel gene therapy approach. We seek an experienced..
OverviewnThe successful candidate will be responsible for the management of the Complaint Handling system, CAs, NCMRs and Deviation systems. The candidate will work closely with the manufacturing team assisting with..
OverviewnThe Manager of Population Health and Quality Management is responsible for oversight of care management team functions including CP supports delivered, population health management, quality management, and service improvement; and..
THE ROLE The ideal candidate will possess: Minimum 4-year degree or equivalent of directly-transferable industry work experience (Engineering or Quality discipline preferred) Minimum of 4 years leadership/supervisory-level experience, and decision-making..
Job Description Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join..
Description Reporting to the Senior Director, GCLP Quality, this individual will assist in the oversight of GCLP activities at CRISPR Therapeutics, its CROs, and third-party laboratories. The successful hire will..