Quality Control Analyst II - Durham

The QC Analyst I will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. · ...

The purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various AskBio departments. · Perform routine and complex execution of molecular biology and biochemistry an ...

The QC Analyst I will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. · ...

The QC Analyst I will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. · Perform routine analytical testing including but not limited to cell-based potency assays. · Maintain laboratory documentation includi ...

The Program Control team will utilize expertise in Cost/Schedule and business management to maximize successful program performance, provide operational awareness to stakeholders and drive value creation to the enterprise. · Financial analysis including detailed program cost/sche ...

We are seeking a Quality Control (QC) Analyst to support a biotechnology client focused on the development of monoclonal antibody drug substance (DS) and drug product (DP) programs. · This individual will contribute to analytical testing, method development support, protein ch ...

A quality control analyst performs routine GMP analytical testing maintains accurate documentation collaborates with departments adheres to SOPs company policies regulatory guidance supports continuous improvement projects within QC AD laboratories. · Perform routine GMP analytic ...

Perform routine analytical testing including but not limited to cell-based potency assays. · ...

We're currently recruiting for a Analyst II to join our Quality Control team. · You will interface with multiple Quality Control functions in support of method qualification, transfer, and validation activities. · ...

+Establish new commercial-level in-house GMP testing laboratories+ · +Perform cGMP analytical testing (ddPCR, qPCR, ELISA and chromatography)+ · +Review and evaluate raw data from a peer or technical review level of all analytical methods+ · ,as well as sample authorization.Respo ...

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. · At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat seriou ...

We are looking for a Senior Analyst to join our Quality Control team. The role involves establishing new commercial-level in-house GMP testing laboratories and performing release and stability testing for multiple stages of our gene therapy and immune oncology products. · Perform ...

We are looking for an Analyst II to join our Quality Control team. In this role, you will interface with multiple Quality Control functions in support of method qualification, transfer, and validation activities. · BS with 3+ years in a biotechnology discipline · 3+ years of expe ...

This Quality Control Analyst will support late-phase and commercial quality control activities. They will execute activities such as raw material testing, release testing, stability testing, · and environmental monitoring. · ...

Kincell Bio engineers cells into therapies. We offer challenging career opportunities competitive benefits and an environment that recognizes and rewards performance. · ...

Join Team Novo Nordisk and help us make what matters. · ...

We are seeking a Quality Control Analyst to join our team in Durham, NC. As a Quality Control Analyst, you will be responsible for performing and reviewing analysis of in-process, release & stability samples in accordance with cGMP, site & corporate procedures & policies. · Leadi ...

We are looking for a Senior Analyst I - QC Bioassay to join our Quality Control team in Durham, North Carolina. In this role, you will be establishing new commercial-level in-house GMP testing laboratories performing release and stability testing for multiple stages of our gene t ...

About this roleWe are seeking a Quality Control Analyst II to join our team in Durham, NC. · As a Quality Control Analyst II at Novo Nordisk you will perform and review analysis of in-process release & stability samples in accordance with cGMP site corporate procedures policies. ...

Assists and supports the organization with initial compliance and ongoing preparation testing and monitoring of conformance to established quality processes and standards for manufacturing production. · Performs Environmental Monitoring and Microbiological testing in support of m ...