Are you a business? Hire regulatory analyst candidates in Bridgewater, NJ
JOB DESCRIPTION:Enter and maintain subscription/connectivity contracts in D365 Quoting and invoicing clients for subscriptions.Support customer billing inquiries and fleet analysis to ensure accurate monthly billing.Monthly contract creation and management in D365 for operating system.Update and ...
JOB DESCRIPTION:Manage the services from contractors, engineers, customers, owners, utility companies, sales staff and service technicians.Maintain responsibility for all technical and financial health of each contract accrual account ensuring gross profit levels budgeted for each job.Identify, d...
Identify, document and report product issues and help identify root causes that affect customer satisfaction, productivity and/or operationsExercise strong problem-solving abilities and collaboration with multiple parties to work through technical and financial issues.
Responsibilities will include all administrative functions for the sales department: managing calendars, scheduling and booking travel, managing correspondence, processing expense reports, planning department meetings, preparing and editing presentat Administrative Assistant, Administrative, Seni...
Apply requirements planning, elicitation, documentation, analysis, communication, validation, and management practices. Work in P&C Insurance applications on with a focus on organizational deliverables, best practices and client management as per the Service Level Agreements.
Working familiarity with research- Pharma Technologies, Scientific.IT Architecture techniques, how to read documents.Experience in Research (Scientific / Pharma domain).
Will consider candidates who commit to becoming ACE certified analysts by completing the Guidewire BA certifications of Associate (InsuranceSuite Analyst certification) within the first six months and the Professional (ClaimCenter specific) certification within the next 12 months. This position w...
Willing to be available 24/7 for emergency technical response and coordination of resources on as needed basis RECOMMENDED QUALIFICATIONS:3-5 year’s experience in a related industry, particularly with large rotating equipmentBachelor’s Degree in Engineering or equivalent experience preferred, b
Compliance and Regulatory Specialist Location: Somerset NJ Schedule M-F 8:30 to 5:00pm On site daily Duration: 3 month contract to hire Education: Bachelor’s degree with at least 5 years of experience working in the pharmaceutical industry in Quality/Regulatory Compliance, Quality Assurance, Qua...
Business/Product Analyst on our Personal Lines IT team, you will serve as a primary point of contact for stakeholders from IT, Underwriting, Operations, Product applications and Finance within our North America personal lines business for feature development, scope management, enhancements, issue...
Analysis of tickets, Create ticket dashboards to improve the SLA and MTTR metrics, Lead ... Experience of working in pharmaceutical industry and knowledge of GxP regulations will be preferred ...
Ensure all operations comply with DOT and industry regulations, safety standards and company ... data analytics. Reporting: * Provide regular updates to the executive team on operational ...
This individual will ensure that our systems (reagent + instrument) meet regulatory standards, function properly, and perform as documented in their respective claims (analytical and clinical). This ...
... regulatory standards. * Maintain knowledge of industry-specific regulations, especially those related to advertising and digital marketing in the pharmaceutical space. * Performance Analysis and ...
... bio analysis regulations, bio markers, pharmaceuticals, GLP/GCLP Job Description: Act as the project manager to support the externalization and operationalization of clinical biomarkers and ...
Must-Have Experience with: biotech, bio analytics, bio analysis regulations, bio markers, pharmaceuticals, GLP/GCLP. Our client is a leading Pharmaceutical Industry, and we are currently interviewing ...
Adhere to food production regulations and guidelines - FDA, EPA, OSHA, GMP etc. and follow and improve site/departmental procedures and policies. * Document, analyze, interpret trial and processing ...
... regulatory authority or EC/IRBs.Provide medical feedback for activities related to review of data for interim analysis or blinded data reviews.Production of tables, listings and narratives of safety ...
