7 results for Quality Control Analyst Jobs in 02138, Cambridge, MA, US

We are seeking a GMP QC Analyst to join our team. This role is responsible for performing quality control testing, ensuring the analysis of raw materials, in-process materials, and finished products in compliance with Good Manufacturing Practices (GMP) and regulatory standards. The QC Analyst will c...

Position Summary:Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, ...

Responsible for performing routine and non-routine assays of raw materials, in-process samples, drug product, and stability samples in the QC laboratory. Conducts QC testing using various laboratory equipment, performs microbial limits and Bioburden testing, assists in reviewing QC data, maintains l...

SummaryResponsible for providing or overseeing the analysis, administration and oversight of comprehensive chemistry/biochemistry policies, programs and practices; may provide feedback and guidance to clients regarding the analysis of materials, products and/or devices utilizing complex to specializ...

About UsPace Life SciencesPace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP commercial product support. For customers with in-house man...

At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking trea...

Responsible for performing quality control testing of raw materials, in-process materials, and finished products. Conducts laboratory testing, analyzes results, maintains documentation, ensures compliance with GMP and regulatory standards, and supports investigations of deviations and non-conformanc...