THE LARGEST COLLECTION OF QA/QC JOBS ON EARTH
Supports PDF, DOC, DOCX, TXT, XLS, WPD, HTM, HTML files up to 5 MB
opens in new window EEO Statement Accommodations Sitemap Job Seekers Protect yourself against identity theft Please be aware there are instances of identity thieves posting Takeda-branded jobs and posing as..
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..
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..
Are you a Music lover? Are you a DJ or a musician? Perhaps you're the technical musician who has a keen eye for detail and loves to understand how the..
Description Westaff is Looking for Quality Control Lab Techs on 3rd shift in Leominster, MA for IMMEDIATE HIRE! Pay: up to $15/hr. based on experience Hours: 11pm-7am | Monday night..
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,..
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..
Job Description CVS Health is embarking on a bold digital agenda to transform health care and empower millions of customers on their path to better health. We are creating innovative..
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..
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..
Description DAVIS Companies has partnered with a leader in Medical Device manufacturing, to identify a Quality Manager for their growing team! Responsible for establishing a US quality system and team..
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..
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..
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..
Job Description As a Software Development Engineering in Test - II, you will support QA activities for Digital projects. You will ensure comprehensive test coverage and achieve efficiency goals through..
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..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease..
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..
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...
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..
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..