- Insmed Incorporated (NJ)
- …serious diseases. In this role, you'll be reporting to the Sr Director, Information Technology Program Management .The Insmed Summer Internship Program ... the Role:We're looking for a Summer Intern - IT Program Management : OKR Framework & Delivery Excellence...pursuing a Bachelor's, Master's, or advanced level degree in Information Systems , Business Administration , Management… more
- Insmed Incorporated (NJ)
- …future of science, we're in. Are you?About the Role:We're looking for a Quality Management System (QMS) Specialist on the Analytical Development team to help us ... Technical Operations department. You will be responsible for managing the Quality Management System (QMS) for the entire Technical Operations department.What… more
- Merck & Co. (Rahway, NJ)
- …and post-market surveillance. Key Responsibilities and Activities: The Senior Scientist, Device System - Device Risk Management will be responsible for device ... the device risk management strategy, including the creation of device risk management plans and reports, conducting system hazard analyses and Failure Modes… more
- Insmed Incorporated (San Diego, CA)
- …as a key team member. \tProvide guidance and support to ensure Insmed computerized systems are deployed following lifecycle management and remain in a validated ... and security requirements. \tEnsure compliance and operational efficiency of validated systems through participating in release management , change control,… more
- Insmed Incorporated (NJ)
- …serious diseases. In this role, you'll be reporting to the Associate Director, Quality Systems . The Insmed Summer Internship Program is designed to give you more ... the Role:We're looking for a Summer Intern - Digital Systems QA on the Quality Assurance Team to help...are invested in your growth. The Insmed Summer Internship Program gives students an opportunity to gain hands-on experience… more
- Insmed Incorporated (NJ)
- …to oversee cybersecurity operations, enterprise risk management , and Computer Systems Validation (CSV) program . This role will manage cross-functional teams ... industries, ideally biotechnology or pharmaceuticals.Bachelor's degree in Computer Science , Information Systems , Cybersecurity , or related discipline (advanced… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Act ("IRA") processes and compliance activities for the Medicare Drug Negotiation Program . Ensures accurate and timely input and implementation of 340B requirements ... policies and procedures and Sarbanes-Oxley regulations. Co-develop processes to validate 340B Program processes as well as MFP refund processes, oversee general … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Master's in Information Systems or similar graduate level management program Experience - Demonstrated experience applying artificial intelligence (AI) ... for the remainder of the internship. Responsibilities:Support Project Portfolio Management (PPM):- Help develop and operate PPM systems... Management (PPM):- Help develop and operate PPM systems and processes.- Apply AI tools to automate and… more
- Merck & Co. (Durham, NC)
- …QA proceed in compliance with cGMP, regulations, and our Company's Quality Management System focusing on batch record review, process/aseptic observations, ... Quality Control Systems , Quality Documentation, Quality Management , Quality Management Standards, Quality Management Systems (QMS) {+ 2… more
- Cipla (Fall River, MA)
- …Warehouse, Quality etc., IT project coordinator role and stakeholder management for systems implementation. Responsibilities/ Accountabilities Application ... support functions and vendors / partners. This role will perform IT Systems Support including Systems Implementation, Validation, Administration etc., for… more
- Cipla (Central Islip, NY)
- …in a pharmaceutical manufacturing lab. Experience and understanding of the Laboratory Information Management Systems (LIMS) is a plus. Understanding ... quality standards and regulatory requirements. Understanding of regulatory compliance, quality management systems and document control processes, and the ability… more
- Butterball (Raeford, NC)
- …tasks. Participates in HR activities such as hiring, terminations, performance management , goal setting, team member development, scheduling, etc. Enforces ... systems , policies, and procedures. . Directs the maintenance and...manner. . Develops, schedules, and controls a preventive maintenance program to maintain production machinery and equipment in proper… more
- Merck & Co. (Durham, NC)
- …Devices, Molecular Microbiology, Quality Auditing, Quality Control Documentation, Quality Control Management , Quality Management Systems (QMS), Quality ... Site Auditor will have leadership responsibility for the site internal audit program , encompassing the full scope of site operations.- Collaboration is required with… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- … program plans. Having experience with global teams, budgetary management , resource planning, and fiscal awareness is preferred.Provide technical expertise of ... Science and Technology team reporting to the Manufacturing Execution Systems Lead and will be responsible for providing project... Lead and will be responsible for providing project management support to the development and administration of EBR… more
- Twist BioScience (South San Francisco, CA)
- …being the creation of high-quality written content and supporting Learning Management System .Daily interaction with technical documentation, with documentation ... set up new or update current Training Plans.Build Training Curriculums.Learning Management System oversight.Provide New Hire overview training.Carries out duties… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Responsible to complete on paper basis audit and to monitor vendor performance management program . Support the issue and communication of audit plans, agenda ... with local procedures and standards. Accountable to track this information on QA electronic system and to...in QA GMP Audit processes for contribution of Quality Management System (QMS) establishment processes in collaboration… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- … management , issues, deviations, corrections, remediation and improvement.Conducts local system data performance monitoring and analysis for BAS and EMS.Executes ... be responsible for providing engineering support for building automation and controls systems in the cGMP Clinical and Commercial Cell Therapy Manufacturing plant.… more
- Merck & Co. (Rahway, NJ)
- …in partnership with project CQV and IT teams.Support establishment of GxP systems in the facility: Change Management , Maintenance protocols, Calibration ... is capable of meeting all historic, currently existing, and cutting-edge biologics program demands from supporting development to pilot scale, small and large scale… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an aseptic manufacturing facility, preferably in training/ system applications, quality systems , or learning management systems .Knowledge of cGMP ... an Operations Unit and collaborate closely with Operations Associates and Management to facilitate readiness of trainees and effective process qualifications. The… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …presentation skills a plus Excellent analytical and computer skills including Excel and material management systems Three to five (3-5) years of experience in a ... experience is a plus, also can consider candidates with other relevant ERP system experience. Our facility manufactures lifesaving medicine for our patients and this… more
