- Merck & Co. (Rahway, NJ)
- …community, provide for and lead Quality Assurance oversight for computer system validation matters within the Global Development Quality organization and for the ... Quality Management System elements into the end-to-end computer system validation process, thereby promoting permanent inspection readiness.Develop and maintain...and exposure with agency regulations, such as 21 CFR Part 11, Part 58, Part … more
- CHRISTUS Health (San Antonio, TX)
- …asthma, RSV/bronchiolitis, failure to thrive, surgical overflow, and behavioral health needs. Be part of a team that is at the forefront of pediatric care and ... validated through successful completion of the designated organizational entry competency validation and a MedSurg specific competency validation .All newly… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate MES Engineer as part of the Manufacturing Excellence team based ... in Raritan, NJ. Role OverviewThe Associate MES Engineer will be part of...including but not limited to Tech Support, Process Improvement, Validation , Supply Chain, Operations, QA, Reg CMC, and IT.… more
- Insmed Incorporated (San Diego, CA)
- …Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director, EDC Programming will lead and oversee EDC programming, ... partners.ResponsibilitiesEDC System Design & Development:Lead the setup, development, and validation of EDC systems, including configuration settings, integration with… more
- Genmab (NJ)
- …feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of compounds as ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication… more
- Merck & Co. (San Diego, CA)
- …in the treatment of immune-driven diseases.This role will report to the Associate Vice President, Immunology Discovery. This position will serve as Discovery ... scientific rationale for target ID through translational research, target validation , differentiation, derisking, modality selection, and overall strategy through… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma.Legend Biotech is seeking Director of Operations as part of the Technical Operations team based in Raritan, NJ. Role OverviewThe ... execute daily production schedules.Will have 3-6 direct reports ranging from Associate Director, Senior Manager, and Manager.Oversee the hiring, development, and… more
- Vorbeck (Jessup, MD)
- …to deliver high-performance material-based solutions. Job Description The Senior Associate , Antenna Research Engineer at Vorbeck will be responsible for ... of system development, from concept and design through modeling, optimization, validation , and final product launch. Ensure the seamless integration of… more
- Ayar Labs (San Jose, CA)
- …an on-site position) Summary: This role is responsible for pre-Si verification and validation of complex SoCs with both high-speed custom and digital blocks. You ... will work in a dynamic startup environment as part of a small IC design team. The ideal...and who can effectively manage his or her own time to take projects to completion with limited supervision… more
- Lilly (Pleasant Prairie, WI)
- …to make life better for people around the world. **Responsibilities:** The Associate Director, Validation is responsible for staffing, training, and leadership ... validation types at the site as needed. The Associate Director will be responsible for supporting the day-to-day...a general overview of the job requirements at the time it was prepared. The job requirements of any… more
- Lilly (Lebanon, IN)
- …clinical trial medicines, while also reducing costs and environmental impact. The Associate Director-Automation Engineering - Control System Validation and Data ... and data engineers that support the daily operations of the facility. The Associate Director is also responsible for the productivity and development of the… more
- Santander US (Coconut Grove, FL)
- Senior Associate - Technology & Cyber Risk Management RCSA Validation Coordinator Country: United States of America **Your Journey Starts Here:** Santander is a ... The Senior Associate will act as a central coordinator for validation activities, working closely with technology and cyber stakeholders, and control testers,… more
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the validation ... and company standards for pharmaceutical/radiopharmaceutical production. This role oversees validation activities from initial planning through execution, manages a… more
- Bristol Myers Squibb (Devens, MA)
- …place than here at BMS with our Cell Therapy team. The **Senior Specialist, Associate Process Validation Engineer, Cell Therapy** provides process validation ... Facility (CTF). The Senior Specialist participates in facility and process validation activities, including process tech transfers and lifecycle management. **Shifts… more
- Merck (Rahway, NJ)
- …community, provide for and lead Quality Assurance oversight for computer system validation matters within the Global Development Quality organization and for the ... Quality Management System elements into the end-to-end computer system validation process, thereby promoting permanent inspection readiness. + Develop...and exposure with agency regulations, such as 21 CFR Part 11, Part 58, Part … more
- Unither Pharmaceuticals (Rochester, NY)
- Computer Systems Validation Specialist Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve ... working, and communicating with personnel across multiple departments. Performs validation activities related to the implementation of computer systems as… more
- PCI Pharma Services (Rockford, IL)
- …across our global network to pioneer and shape the future of PCI. The ** Validation Analyst III** is responsible for overall validation project ownership of large ... mild supervision. Responsible for the generation and execution of validation protocols, assistance in audits, and determination of ...adherence to all PCI, cGMP, GCP, GAMP, 21CFR, 21CFR Part 11, and Annex 11 policies, procedures, rules, and… more
- PCI Pharma Services (Rockford, IL)
- …across our global network to pioneer and shape the future of PCI. The ** Validation Analyst II** is responsible for overall validation project ownership of ... mild supervision. Responsible for the generation and execution of validation protocols, assistance in audits, and determination of ...adherence to all PCI, cGMP, GCP, GAMP, 21CFR, 21CFR Part 11, and Annex 11 policies, procedures, rules, and… more
- Catalent Pharma Solutions (Kansas City, MO)
- **Quality Engineer II, Validation ** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... supporting product development, launch, and full life-cycle supply. With time -tested experience in development sciences, delivery technologies, and multi-modality… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- The QA Validation Fill Finish team is hiring a Manager!...the following years of experience for each level: + Associate Manager: 6+ years + Manager: 7 + years ... As the Manager, QA Validation you will validate/qualify equipment, systems, and processes related...programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron… more
