- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible ... the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must actively support, participate and embrace an empowered team culture… more
- Aequor (Devers, TX)
- …the needs of the business warrant.JOB SUMMARY is seeking a Contractor Field QA Specialist for the QA Operations organization at the LSCC in Devens, MA. The ... Contractor Field QA Specialist is responsible for quality activities for the LSCC...with applicable procedures and batch records. Perform real time review of manufacturing batch records. Review manufacturing… more
- Novo Nordisk Inc. (Boulder, CO)
- …are driving change. Are you ready to make a difference? The Position The Specialist , API Manufacturing works in Novo Nordisk's Boulder, Colorado Pilot Plant and is ... ensuring the supply of API and meeting production goals, the Specialist , API Manufacturing actively supports continuous improvement initiatives and identifies… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- … management procedures, including business engagement, impact analysis, documentation review and approval, user testing reviews, ensuring smooth and controlled ... Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of the Technical Operations team based...and collaborate in the design-implementation of Legend's Master Data Management program. We are looking for a well-organized and… more
- Merck & Co. (Millsboro, DE)
- …on time, every time, across the globe.The Quality Control (QC) Associate Specialist , with Guidance from the QC Manager, ensures product/process quality through the ... review of GMP documentation and performs activities to ensure...release of antigen and seed batches. The QC associate specialist must adhere to regulatory and site policies and… more
- Catalent (Manassas, VA)
- POSITION SUMMARYThe Quality Assurance Specialist I is responsible for inspection and verification of the products and production processes along all the production ... ensure adherence to company quality standards procedures and policies. Inform the QA management if any out of specification or any deviations are found. Comply with… more
- Merck & Co. (Rahway, NJ)
- …dedicated colleagues while developing and expanding your career.The Senior Trial Initiation Specialist in Global Site Budgets and Payments will be responsible for ... guidance and work with stakeholders to prepare such guidance for review /approval.Identify and promote best practices. Adhere to SOPs, ethics and departmental… more
- Catalent (St. Petersburg, FL)
- …controls in all applicable areas of the manufacturing operation. The Senior QA Specialist will assist in organizing and prioritizing the activities and schedule for ... compliance enhancements/improvements and leading project to deliver solutions.Collaborates with management and supervisory personnel from operations, quality control and… more
- Merck & Co. (Durham, NC)
- …medicines and vaccines, including our HPV vaccines. - The Senior Engineering Specialist will troubleshoot and maintain process and process support equipment utilized ... projects for equipment/maintenance related improvements, including obtaining quotes, drawing/specification review /approval, and review of contracts. Interact with… more
- Merck & Co. (Rahway, NJ)
- …to work in a fast-paced job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:Site Operations (GWES)… more
- Novo Nordisk Inc. (San Antonio, TX)
- …obesity to maximize sales within an assigned territory. The Obesity Care Specialist (OCS) must achieve sales goals by implementing marketing and sales strategies ... with those individuals Recognize opportunities to productively challenge HCPs clinical management of patients that respects their knowledge and experience and adds… more
- Merck & Co. (Durham, NC)
- …direct in-line Quality support for all compliance and environmental monitoring matters, review of atypical events including accessing product impact for EM events, ... providing Quality oversight to alarm events during processing, review and approval of incursions, review and approval of batch record documentation, and… more
- Merck & Co. (Rahway, NJ)
- …to work in a fast-paced job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:The automation engineer… more
- Novo Nordisk Inc. (Philadelphia, PA)
- …access and drive business impact by collaborating around the clinical management of patients and offering NNI-approved solutions Demonstrates professionalism and a ... by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications Bachelor's or equivalent degree, and/or Pharm… more
- Merck & Co. (North Wales, PA)
- …development/maintenance of presentation trackers, document trafficking, author travel request management , archival of final versions and QR code process.Manage ... flow to/from internal and external service providers, joint venture document review and clearance and independent manuscript review .Tracking and reporting… more
- Merck & Co. (Rahway, NJ)
- …submissions for assigned products.- Leading cross-functional teams to develop, review and approve Core and Local Labeling documents.- Recommending strategies ... Regulatory Affairs, Clinical, Pharmacovigilance).- - Required experience and skills: Project management skills with the ability to handle multiple projects and… more
- Novo Nordisk Inc. (Durham, NC)
- …in the pharmaceutical or medical device industry General knowledge of Batch Review Processes (BRP), validation processes and Quality Management Systems (QMS) ... (BPRs) & relevant quality processes are compliant with regulations. Performs quality review & approval of Change Requests (CR's) & other documentation (in… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking a CQV Specialist (Contract Position) as part of the Technical Operations team based in Raritan, ... be responsible in handling day-to-day activities inclusive of execution, protocol management , vendor management , issues, deviations, corrections and remediation… more
- BioAgilytix (Durham, NC)
- …ResponsibilitiesPerform Quality Control (QC) technical, scientific, and compliance review of data and documentation generated by the Bioanalytical ... OOS and OOT associated with Bioanalytical Operations data as applicableIssue QC review observations and work closely with the scientific staff to ensure data… more
- Novo Nordisk Inc. (Philadelphia, PA)
- …productively and respectably challenge and influence target physicians' approach to patient management and adds value by sharing new information and unique insights ... with target physicians Recognizes opportunities to productively challenge HCPs clinical management of patients that respects their knowledge and experience and adds… more
