Job Description Job Title: Documentation Management Specialist Job Grade: Analyst 502 LOB: Digital Document Services, CIB Operations Full time/Part time: Full Time The Digital Documentation Services (DDS) Operations teams are responsible for supporting all JPM businesses for their
Job Summary: Provides empathetic pharmacy consulting services to patients regarding the effective use of medications and drug interaction awareness. Offers preventive and clinical healthcare services, including immunizations, diagnostic testing, and patient outcome services. Ensures prescribed medications
About Flexport: At Flexport, we believe global trade can move the human race forward. That’s why it’s our mission to make global commerce so easy there will be more of it. We’re shaping the future of
Company Description Since its spin-off in September 2025 AUMOVIO continues the business of the former Continental group sector Automotive as an independent company. The technology and electronics company offers a wide-ranging portfolio that makes mobility safe,
Job Overview: The Senior Clinical Research Associate monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Company and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International
Job Description: Essential Job Functions: • Conduct quality control and assurance activities, including inspections and testing, to ensure product compliance with established standards and procedures. • Analyze quality data and metrics to identify areas for improvement and
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
CRA I - Guangzhou Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate
Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our
The EHS & Facility Supervisor is responsible for ensuring EHS compliance, DHR/SCIEX EHS Policy Deployment, related EHS program implementation, and managing site level facility work (e.g. installation, repairing, preventive maintenance, etc.). Lead site-level EHS compliance management,
At Jabil (NYSE: JBL), we are proud to be a trusted partner for the worlds top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network
Background Diversity, Equity and Inclusion are core principles at UNDP: we value diversity as an expression of the multiplicity of nations and cultures where we operate, we foster inclusion as a way of ensuring all personnel
Typical Accountabilities - Coordinate lifecycle management, enhancement, and business continuity for Study Delivery processes, systems, reporting, and technology across the clinical research portfolio. - Develop, implement, and continuously improves reporting tools, metrics, and analytical processes, identifying
Location:Hefei, Anhui, China Job ID: R0136424 Date Posted:2026-07-06 Company Name:HITACHI ENERGY HEFEI TRANSFORMER CO., LTD. Profession (Job Category):Production & Skilled Trades Job Schedule: Full time Remote:No Job Description: Responsible for performing various tasks in the manufacturing
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical trials
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative
Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative
Job Description Come Make the World With Us MBD Sr Project Engineer , is integral part of our Software Engineering organization. This position take responsibility of Model based Design Software Platform for next Gen Product and
Work Flexibility: Onsite Continuously fully comply will all GMP standard requirements. 完全遵守GMP的相关要求。 Responsible to stop further processing in the event of encountering non-conforming products condition. 当遇到产品异常时，有责任停止继续生产。 Will perform repetitive to frequent tasks using standard procedures and various