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Job Title : QA Associate - ITFLSA Classification : Full-Time, Exempt ProfessionalWork Location : Fall River, MAWork Hours : General: 8:00AM - 5:00PM (May vary based on business needs)Reports To : Site

Job Title : QA Associate - IT FLSA Classification : Full-Time, Exempt Professional Work Location : Fall River, MA Work Hours : General: 8:00AM – 5:00PM (may vary based on business needs) Reports To :

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.We are PCI. Our investment is in People who make an impact, drive progress and create a better tom

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.We are PCI. Our investment is in People who make an impact, drive progress and create a better tom

We’re looking for a Senior Quality Assurance Associate who enjoys being close to the product, the process, and the people. In this role, you’ll be a key contributor to ensuring our finished goods meet

QA Receiving AssociateRadwell International LLC – Receiving DepartmentPosition: Full‑time, Hourly, On‑siteSchedule: Monday–Friday – 7:00 am to 4:00 pmLocation: Glendale, AZ, USAddress: 7860 N 106th Av

DescriptionThe QA & QC Lead Analyst is a demonstrated quality professional who operates independently across both Quality Assurance and Quality Control within the Mortgage Default and Servicing space.

Description The QA & QC Lead Analyst is a demonstrated quality professional who operates independently across both Quality Assurance and Quality Control within the Mortgage Default and Servicing space

OverviewThis role is responsible for ensuring compliance with Quality Assurance (QA) and regulatory requirements within GMP operations. The Primary responsibilities include audits, documentation revie

QA Receiving Associate Radwell International LLC | Receiving Full-Time | Hourly | On-site Schedule: Monday–Friday – 7:00am to 4:00pm 7860 N 106th Ave, Suite 170, Glendale, AZThe QA Receiving Associate

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work

QC Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the quality control plan. This includes working with employees as wel

Senior QA Associate KVK Tech is seeking a Senior QA Associate to join our team in Newtown, PA.The Senior QA Associate will serve as a key Quality Systems subject matter expert (SME), supporting multip

OverviewJoin to apply for theTemp-QA Associaterole atAlkermes . This is a temporary position. ResponsibilitiesIssuance of GxP documentation. Document Management System Support. Support documentation l

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmace

Job TitleFacilitator for Sponsor Audits and Regulatory Inspections Job DescriptionThe successful candidate will be responsible for facilitating the management of sponsor audits, a broad range of regul

We are a global healthcare leader headquartered in Indianapolis, Indiana, committed to discovering and bringing life‑changing medicines to those who need them.Organisation Overview Lilly is entering a

About Artiva: We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for

Job SummaryThe QA associate for documentation ensures compliance with cGMP and internal policies, procedures, and specifications. This position is responsible for performing inspections, batch record

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.Job Title QA Associate

Overview TUV SUD America Inc., a global leader in testing, inspection and certification, has an immediate opening for a Documentation QC/QA Associate based in Peabody, MA.ResponsibilitiesAssist certif

ResponsibilitiesReview, approve, and release manufacturing, packaging, and clinical batch records along with auxiliary documentation. Prepare product release summaries and create Certificates of Analy

As a pivotal member of our quality control team, the QA Associate plays an essential role in upholding the high standards that our company is known for. This position involves meticulous oversight of