When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
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 according to
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans,
Job Family Group: Operations Group Job Description: As a Production Engineer, you will work closely with the Operations Manager and site leadership team to learn, contribute and grow in a lubricant blending manufacturing environment. This role
About this Position Execute production plans and conduct variance analysis to achieve the Production Department’s KPI targets. Implement production standard operating procedures (SOPs) and training requirements to ensure shift personnel possess the required competencies. Manage shift teams to meet
Job Purpose/summary This role will execute a detail-oriented and proactive individual to join our team as a Night Shift Data & Performance Maintenance Analyst. This role is critical in ensuring the smooth operation of our reporting
Day to Day Responsibility Lead and drive plant excellence / process excellence initiatives to improve operational performance across the site. Identify, prioritize, and implement continuous improvement projects focused on productivity, quality, cost, delivery, and safety. Facilitate
Job Description It is critical that, for all company-sponsored clinical trials, patient safety, high-quality data, and compliance with company requirements and regulations are delivered and sustained. The Country Clinical Quality Manager (CCQM) position has a significant
JLL empowers you to shape a brighter way. Our people at JLL are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are
Job Description SummarySystems engineering is a cross-functional engineering discipline centered on an approach, mindset, and process. All activities that consider both the business and the technical needs of the customers with the goal of providing a
JOB SUMMARY Responsible for the management of all aspects of the Catering and Conference departments in accordance with company and brand standards. Coordinates details and menus for clients functions and maintains budgeted revenues through solicitation of business.
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Job Group Capability Engineering Job Group Automation & Process Control Why Join Us Join a leading Oil & Gas company and bring your expertise in instrumentation, controls, automation, and reliability to support safe, reliable, and high-performing
Why Join us Join a leading Oil & Gas company and build your career in instrumentation, controls, automation, and asset reliability. As an Associate Instrument Engineer, you will support the design, application, troubleshooting, and improvement of
About Ampd Energy Ampd Energy is transforming how cities build - cleaner, smarter, and more sustainably. We are trailblazers in making the construction industry emission-free. Our products are advanced, compact, and connected battery energy storage system
Main Purpose of the job 职务目的： Responsible for supplier quality management, quality control, problem solving, and quality level improvement. 负责供应商质量管理，质量监控，问题解决，质量水平提升 Job Responsibilities工作职责 Participate in the continuous improvement process of the plant, manage the plant quality system
Job Title: Research Integrity Adviser Location: Beijing, Shanghai or Nanjing, China About Springer Nature Springer Nature is one of the leading publishers of research in the world. We publish the largest number of journals and books
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans,
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 according to