Automation Engineer, GMP - Pennington, NJ

The Automation Engineer is responsible for administration and management of the site's automation systems. · ...

The Automation Engineer is responsible for administration and management of the site's automation systems. · ...

+6 años de experiencia en validación GMP o entornos similares · Experiencia mínima de 10 años en validación GMP · Capacidad para analizar datos y priorizar tareas · Tecnología: biology, MS-Word, MS-Excel, MS-Outlook , PowerPoint ...

This Manufacturing Associate supports both Upstream and Downstream manufacturing operations in a cGMP-compliant environment. · Support cell culture to protein purification process · ...

In this role, you'll operate, inspect, and maintain mechanical and electrical equipment in assigned facilities in GMP and Non-GMP environments to achieve the most efficient results. Assure that equipment is being maintained safely. Minimize downtime through proactive performance ...

The Manufacturing Associate will be responsible for day-to-day operations of downstream processing in a clean room environment. · Prepare and maintain buffers and media required for downstream processes. · Operate and maintain chromatography systems for protein purification. · ...

The Manufacturing Associate will be responsible for the day-to-day operations of downstream processing in a clean room environment. · This role includes buffer and media preparation chromatography tangential flow filtration TFF viral filtration and aseptic processing.Prepare and ...

+The QC Raw Material Associate will be primarily responsible for assisting with material inspection, · +Participate and support the inspection, sampling and testing of incoming raw materials and consumables. · Review all material related documentation including supplier documents ...

The position is ideally suited for a professional with extensive technical knowledge and a proven track record of developing and carrying out processes suitable for use in GMP manufacturing of a wide range of clinical trial materials. · ...

The QC Raw Material Associate will be primarily responsible for assisting with material inspection. · Assisting with material inspection. · Data entry and documentation of incoming materials to ensure they meet company specifications and regulatory standards. · ...

Manages all Quality Control (QC) laboratory instrumentation and metrology activities to support GMP manufacturing testing and release of materials intermediates and finished products under FDA/EU regulations applicable international regulations and BeOne processes procedures. · ...

The Technician/Specialist will work within the Upstream Processing group and performs activities in upstream operations such as preparation of stock solutions, buffers and media. · Filtration of stock solutions, buffers and media. · Set-up and operate disposable fermenters / bior ...

A leading biology research company in rapid expansion seeks a Senior Procurement Manager. · ...

About GenScript GenScript Biotech Corporation is a global biotechnology group. Founded in 2002 it has an established global presence across North America Europe the Greater China and Asia Pacific Job ScopeThe position reports to the Sr QC Manager is ideally suited for a professio ...

The position is ideally suited for a professional with extensive technical knowledge and a proven track record of developing and carrying out processes suitable for use in GMP manufacturing of clinical trial materials. · Support in the set-up, development and optimization of GMP ...

This role is ideally suited for a dynamic bench-focused individual to support/lead translation of research process to GMP-compliant manufacturing, and will develop, scale-up, and evaluate the technology transfer of viral vector processes. · Bachelor's degree with 3-7 years, or Ma ...

The Scientist Upstream Process Development role is a dynamic position that supports and leads the translation of research processes to GMP-compliant manufacturing. The successful candidate will develop, scale-up, and evaluate the technology transfer of viral vector processes in a ...

A leading biology research company seeks a Senior Procurement Manager to design strategies for optimal cost control and enhance vendor management. · ...

This role combines hands-on laboratory work with strategic process development and cross-functional collaboration. · The Scientist will develop, scale-up and evaluate technology transfer of viral vector processes in fast-paced biotechnology environment. · ...

We are a global biotechnology group founded in 2002. · We proactively provide end-to-end CDMO services for drug discovery to commercialization. · ...