Data Entry Associate The Data Entry Associate is responsible for recording and validating information to be recorded and transmitted to other MasTec offices, personnel, and customers. This position supports MasTec office operations and works cross-functionally with other departments.
Advanced CQV Consultant As an Advanced CQV Consultant you are responsible for the planning, execution, and delivery of commissioning, qualification, and validation (CQV) activities within pharmaceutical, biotechnology, and life science projects. This role independently executes complex CQV
Roche Digital Validation System Strategy Leader At Roche, we believe its critical to deliver medical solutions now even as we develop innovations for the future. We are passionate about transforming patients lives and we are fearless in
Data And Analytics Manager The Data and Analytics Manager supports the Colleges mission by transforming institutional data into actionable insights that inform strategic planning, enrollment forecasting, institutional effectiveness, and student success initiatives. This position is responsible for managing and
Service Enablement & Continual Service Improvement Manager Location: NC-Clayton, US Contract Type: Regular Full-Time Area: INFORMATION SYSTEMS Would you like to join an international team working to improve the future of healthcare? Do you want to
API Manufacturing Associate I (Night Shift) Facility: Manufacturing Location: Clayton, NC, US About the Department At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For more than 100
Modeling And Simulation Manager Research Triangle Park, NC Vulcan Elements is manufacturing American rare-earth permanent magnets for a secure, resilient future. With a focus on national security and economic resiliency, we serve critical industries such as
Manager, All-QC Team The Manager, All-QC team is responsible for contributing to key functional, tactical, and operational aspects of the QC group and will lead the 223-shift teams that are responsible for performing routine testing required
Senior Manager Instrumentation and Maintenance Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all
Senior Quality Compliance Specialist Welcome to Holly Springs, North Carolinahome to Roche/Genentechs largest-ever investment: a $2B greenfield start-up where next-generation technology, high-performing teams and operational excellence converge to create the global standard for high-volume, highly-efficient drug
Quality Assurance Specialist -Supplier Quality Welcome to Holly Springs, North Carolina home to Roche/Genentechs largest-ever investment: a $2B greenfield start-up where next-generation technology, high-performing teams and Operational Excellence converge to create the global standard for high-volume,
Operations Lead Welcome to Holly Springs, North Carolinahome to Genentechs largest-ever investment with an ambitious goal to be a fully connected Plant of the Future. This is where next-generation technology, capability, digital connectivity and Operational Excellence
Production Planning & Forecast Specialist Location: NC-Clayton, US Contract Type: Regular Full-Time Area: MANUFACTURING Req Id: 543456 Would you like to join an international team working to improve the future of healthcare? Do you want to
Position Overview The Supply Chain Planner 3 role supports the project phase and operations of GMP Purchasing and Supply Chain Planning at Fujifilm Biotechnologies to ensure that the right materials are available at the right time,
Position Overview The Supervisor, Quality Assurance Operations is responsible for providing supervision and risk-based QA support for the Drug Substance Manufacturing areas and processes. Company Overview FUJIFILM Biotechnologies is building the future of bioproduction in Holly
Position Overview The Associate Director of Commissioning, Qualification, and Validation (CQV) is responsible for leading and executing CQV activities for a large-scale biologics manufacturing facility in compliance with regulatory requirements, including 21 CFR Parts 11, 210, and
Sr IT Compliance Analyst Facility: Digital & IT Location: Clayton, NC, US At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For more than 100 years, we have
Information Systems Sr. Manager Technology Regulatory Compliance Lead Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with
Holly Springs Warehouse Operator Pharma Technical Manufacturing (PTM) is responsible for managing all aspects of end-to-end drug substance and drug product manufacturing and supply. From the raw material to the final medicine, we contribute to deliver
Senior Manager Manufacturing System Engineering - Bulk Drug Substance - Upstream Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve