About the job Sanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China (IFB). For this green field operation, we’re enhancing our legacy of excellence and build
Pharmacovigilance Advisor Play a critical role in patient safety while ensuring compliance across one of our most important growth markets. Your new role As a Pharmacovigilance Advisor, youll be instrumental in maintaining the highest safety standards
Company: Qualcomm China Job Area:Engineering Group, Engineering Group Systems Engineering General Summary: We are seeking a highly skilled expert with a strong theoretical foundation and hands-on engineering capabilities, specializing in motion planning and control of robotic
Job Description: ACCOUNTABILITY Telephony &Video Conference Design & Architecture: Collaborate with global IT teams and business units to design and evolve complex, secure, and resilient IP telephony and video conferencing architectures for Airbuss worldwide operations. Develop
Wood Mackenzie is the global leader in analytics, insights and proprietary data across the entire energy and natural resources landscape. For over 50 years our work has guided the decisions of the world’s most influential energy
We exist to create positive change for people and the planet. Join us and make a difference too! Job Title: Employee Relations Specialist Location: Beijing, Greater China About the role We are looking for an Employee
We exist to create positive change for people and the planet. Join us and make a difference too! Job Title: Regional HR Manager - North-East Asia Location: Beijing, China About the role We are looking for
About the job Sanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China (IFB). For this green field operation, we’re enhancing our legacy of excellence and build
Job Overview Provide project related support; assist with designing, loading, and validation of Lab databases using Clinical Trials Management System(s); ensure work is conducted in line with standard operating procedures, policies and good practice. Accountability and ownership
Are you an enthusiastic individual ready to join a team as a Conference Content Executive? Would you love to be the key onsite representative of Elsevier and serves as a primary liaison between the various stakeholders
Are you an enthusiastic individual ready to join a team as a Conference Content Executive? Would you love to be the key onsite representative of Elsevier and serves as a primary liaison between the various stakeholders
Job Overview: The Contracts Specialist II (CS II) works in collaboration with project teams and the Contracts Lead (CL) to perform key study start-up tasks related to site contracts in their country, or countries, of expertise.
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
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs)
The group you’ll be a part of The Customer Support Business Group focuses on enabling our customers with premier customer support throughout their lifecycle with Lam. We drive performance, productivity, safety, and quality of customers installed
Murex is a global fintech leader in trading, risk management and processing solutions for capital markets. Operating from our 19 offices, 3 400 Murexians from over 65 different nationalities ensure the development, implementation and support of
Use Your Power for Purpose Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing
Job Title: Clinical Research Associate Job Location: China Job Overview: The CRA monitors investigational sites to ensure subject safety and provide quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures
Location:Beijing, China Job ID: R0133337 Date Posted:2026-06-05 Company Name:HITACHI ENERGY POWER SYSTEM CO., LTD. Profession (Job Category):Administration & Facilities Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy is a global technology leader that