Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter –
Work ScheduleStandard (Mon-Fri) Environmental ConditionsSome degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description When you’re part of the team at Thermo Fisher Scientific, you’ll do important
Job Responsibilities Evaluate and select appropriate manufacturing processes for mechanical components to ensure design feasibility, mass production readiness, and efficient assembly. Follow up on trial production and mass production of mechanical parts, develop and optimize manufacturing
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
Company Description Do you want beneficial technologies being shaped by your ideas? Whether in the areas of mobility solutions, consumer goods, industrial technology or energy and building technology - with us, you will have the chance
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
Typical Accountabilities: - In partnership with AZ enablement team, other AZ clinical experts and external service providers, the GSAM provides oversight to ensure study delivery. - Leads/contributes to the preparation of delegated study documents (e.g. Informed Consent
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
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
Career CategoryClinical Development Job Description HGRAC and Operation Excellence Senior Manager lead internal HGRAC management and clinical operation excellence to support high efficiency HGRAC and clinical operation activities and accelerate the trial execution in China. HGRAC Affairs.
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
At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run
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: Lead Technician, QC City, Country: Qingyuan, Guangdong, China On-site We are looking for a responsible and experienced Lead Technician, QC to join the QC team in Qingyuan. In this role, you will perform routine
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
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all
JOB PURPOSE 工 作 目 的 Summarizes the job’s purpose or role and why it exists in the organization 概 述 工 作 的 目 的 或 角 色 及 其 在 机 构 内 的
JOB PURPOSE 工 作 目 的 Summarizes the job’s purpose or role and why it exists in the organization 概 述 工 作 的 目 的 或 角 色 及 其 在 机 构 内 的