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
Local Unit & Position Description Description of Group Contracts Advisory Group Contracts Advisory is a new centralized function established to provide high quality contract review, negotiation and support to the following DNV business areas: Maritime, Business
Company Description Thenamaris is a global ship manager of high specification modern ocean-going vessels. We help deliver goods to people around the world, enriching their lives. We do this by safely managing a world class fleet
ABOUT QUINCE Founded in 2018, Quince was built to challenge the idea that nice things have to cost a lot. Our mission is simple: to make really high quality essentials for really low prices, produced fairly
中国，上海; 南通，中国 | 全职 | Job ID: 10361 About the role: About the Role: The IT system validation manager is responsible for the validation of the IT systems (largely SAP S4HANA), which shall operate in compliance
Shanghai, China | full time | Job ID: 11516 Your contribution: Represent External QC Network at CMOs (predominantly located in China) ensuring QC and GMP requirements of BioNTech are considered Represent external/global QC in multidisciplinary project
Role Summary: The Development China Clinician is responsible for high quality and timely delivery of one or more interventional clinical trials for R&D. They apply technical excellence in the design of cost-efficient clinical trials to meet
Job Description EXTERNAL QUALITY ASSURANCE -Senior Specialist Qualified Person (QP) China The Position The Product Quality Manager (PQM) Senior Specialist is responsible for ensuring that all Company products managed by External Quality Assurance (EQA) are manufactured,
职位描述 End-to-End Product Cost Management -Responsible for target product and production cost calculations across all lifecycle phases – from initial concept to end of production. -Conduct top-down, bottom-up, and greenfield target cost analyses, considering CO₂ targets and
中国，上海 | 全职 | Job ID: 11584 Position Summary: Supports and oversees the proactive and risk-based quality strategy implementation in the drug research and development activities Your main responsibilities are: The Associate Director Clinical QA Compliance
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
We Offer Joining Maersk, you will become part of the global family of the company that moves 20% of global trade every day all the way, where one of our core values is Our Employees. It
Job Description: PURPOSE: Assist Q&FS manager to perform the QC function, assure QC performance compliance with the requirements of Mars Q&FS and Safety requirement. This position is the key position of quality and food safety. DIMENSION:
Job Description Buying Quantification Ensure sum of customer group plans are in line with total aggregated plan per Continent/ Planning Market Responsible to translates Sales Markets’ bottom-up demand plans into supply plans and buying volumes per
We Offer Joining Maersk, you will become part of the global family of the company that moves 20% of global trade every day all the way, where one of our core values is Our Employees. It
1. Project schedule Management ·Build a project team ·Develop and update the project plan, adjust the plan in case of deviation ·Assign tasks to team members and follow up them before task accomplished 2. Project Cost Management ·Control product
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
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
1、Quality Assurance & Inspections and Internal Audit Assists with the timely implementation of applicable quality management systems (SOPs) within the PCO. Assists with ensuring initial and continuous training programs are implemented and maintained for all relevant PCO
Job Mission Business Partner for site managers/CS managers, to execute strategies to assure effective EHS systems, programs and procedures to improve employee safety, reduce operation risk, and avoid any EHS violation in customer sites. Ensure compliance