Mgr., Biologics External Mfg. Quality - Raleigh, NC

We're seeking a highly-motivated individual to join our team as Biologics External Manufacturing Quality Manager. · Review and approve batch records for DS and DP manufacturing, ensuring compliance and data integrity. · Assess and approve deviations, investigations, and CAPAs rel ...

We're seeking a highly-motivated Quality Manager to provide quality oversight for Eisai's biologics products manufactured at external partners. The role ensures compliance with global GMP requirements and Eisai standards across product lifecycle. · Review and approve batch record ...

We are a device-agnostic integrated multi-technology communication platform providing flexibility to balance technological capabilities with economic needs. Trilliant is committed to best-in-class solutions empowering our customers and their customers to connect to the world of t ...

In this Sr. Manufacturing Specialist I role, you will be responsible for manufacturing support tasks including technical writing, project management, and process implementation. · Medical insurance · Dental and Vision insurances · Fitness & Wellness programs including a fitness ...

This Sr. Manufacturing Specialist I role involves manufacturing support tasks including technical writing, project management and process implementation. The position requires a highly detail-oriented individual with excellent technical writing skills and a continuous improvement ...

The Manufacturing Support Engineer works within cross-functional teams to support internal manufacturing operations. Provides technical support to the engineering of novel particles for drug delivery during bulk manufacturing as well as manages manufacturing deviations and CAPA's ...

The intern will assist in understanding root cause for key customer Quality issues. · ...

The role requires 10-15 years of client-facing experience in SAP Transportation Management with expertise in end-to-end SAP S/4HANA Embedded TM implementations and roll-out projects. · ...

Lead consultant for SAP Transportation Management with 10+ years of experience in client-facing roles. Expertise in end-to-end SAP S/4HANA Embedded TM implementations and solution architecture. · Support cutover, go live, and post-go live issues. · Provide solutions for problem s ...

The In-Process Quality Engineer is responsible for monitoring formulation, filling, sterilization, and packaging operations for compliance to site SOPs and cGMP including timely review of cGMP documentation at designated critical process points. · Monitor compliance to meet or ex ...

This position is not eligible for visa sponsorship. Conducting regular evaluations of the system architecture and collaborating with project management teams to improve the designs. · Creating and implementing solutions that are scalable, reliable, and high quality. · Evaluating ...

The In-Process Quality Engineer is responsible for monitoring formulation filling sterilization and packaging operations for compliance to site SOPs and cGMP including timely review of cGMP documentation at designated critical process points. · ...

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. · ...

This position involves conducting regular evaluations of system architecture and collaborating with project management teams to improve designs. The role requires creating scalable, reliable, and high-quality solutions while evaluating project constraints and devising alternative ...

The role of SAP TM Functional Consultant involves providing solutions and recommendations for problem statements/requirements with standard SAP and custom solutions as necessary. The consultant will support cutover, go live, and post-go-live issues while understanding CALM proces ...

This position requires evaluating system architecture and collaborating with project management teams to improve designs. · Evaluating any project constraints and devising alternatives to reduce risks whilst performing process re-engineering. · ...

+The In-Process Quality Engineer is responsible for monitoring formulation, filling, sterilization, and packaging operations for compliance to site SOPs and cGMP including timely review of cGMP documentation at designated, critical, process points. · + ...

This is an IT Solutions Architect position with responsibilities including conducting regular evaluations of the system architecture and collaborating with project management teams to improve the designs. The job requires creating and implementing scalable, reliable and high-qual ...

This is a Quality Assurance Senior Associate role. · ...

In this Sr. Manufacturing Specialist I role, you will be responsible for manufacturing support tasks including technical writing project management and process implementation. · Author manufacturing documentation including procedures work instructions logbooks changeover protocol ...