Postdoctoral Scientist Cell Engineering Research Category Life Science Employment Type Contract Reference BH 364752 Postdoctoral Scientist Cell Engineering Research Why Yoh? Yoh knows greater talent, that's why. The postdoctoral position is a research position in an industrial setting with the opportunity to collaborate across multiple disciplines that is afforded by a la

Postdoctoral Scientist Cell Engineering Research Category Life Science Employment Type Contract Reference BH 364752 1 Postdoctoral Scientist Cell Engineering Research Why Yoh? Yoh knows greater talent, that's why. The postdoctoral position is a research position in an industrial setting with the opportunity to collaborate across multiple disciplines that is afforded by a

The DM analyst is responsible for evaluating Deviations to identify patterns and trends, monitor trend investigations E2E including CAPAS and EC to eliminate trends, perform analysis of deviation data and summarize information for Annual Product Quality Review and other required reports. Notification to management of identified trends. Some of the Your Responsibilities Re

Position is scheduled for Wed Sat 8 00 pm 6 00 am (3rd shift) This is 100% onsite position. The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site, including the coordination, issuance, reconciliation, and management of production labels and records. To succeed in this role, you will have a stron

Manage and coordinate activities associated with the GxP IT Quality Assurance (QA) program for GPS and R&D computerized systems regulatory compliance across the end to end product lifecycle (GPS and R&D) for software development and validation lifecycle activities associated with regulated computerized systems to ensure conformance to cGxPs, guidance documents, applicable

100% onsite M F 1st shift (normal business hours) Senior Specialist, QA Operations, is responsible for quality oversight on Gene Delivery Clinical Manufacturing Facility (S6A) in Summit, NJ and will ensure activities performed are in accordance with policies, standards, procedures, and Global cGMP requirements. This position reports to the Senior Manager of Quality Assura

100% onsite M F 1st shift (normal business hours) Specialist, QA Operations, is responsible for quality oversight on Gene Delivery Clinical Manufacturing Facility (S6A) in Summit, NJ and will ensure activities performed are in accordance with policies, standards, procedures, and Global cGMP requirements. This position reports to the Senior Manager of Quality Assurance Ope