About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScripts businesses encompass four
Career CategoryQuality Job Description Description Quality and Compliance oversight of External sites. Ensure External site activities are in alignment with applicable product CTA /Marketing Application. Key Responsibilities Serve as the main Quality point of contact related
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all
I – JOB INFORMATION Job Title: External Manufacturing Vx PPM and Operations Lead, Japan Effective Date: 3/1/2025 Department: External Manufacturing, Japan Division: EM&S Reports to: Head External Manufacturing Japan Location: Hatsudai, Tokyo. II - JOB SUMMARY
Responsibilities: • Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals it needs to conduct its current and future business activities; and produce, sell, and distribute
This is what you will do: The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion’s product/s across the product/s life cycle. He/she is a peer
Job Description Summary Job Purpose: Monitor and communicate regulatory intelligence and policy information to facilitate decision making for compliant and quality global development aligned with business objectives. Job Description EMajor accountabilities: Monitor and search relevant laws,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description The APJ Purification (PUR) Staff Scientist harmonizes with global Go-To-Market vision by ensuring regional alignment with PUR business unit (BU) metrics. A successful candidate plays a leading role to
We will use your ability to integrate/apply knowledge of global & Japanese regulations governing drug development to progressing Regenerons portfolio. This includes preclinical and clinical drug development programs, policies, and procedures. This is an exciting opportunity
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, youll be
As member of Regeneron’s newly created Japan country organization, you will be responsible for supporting the creation and execution of local commercialization activities focused on the REGN sales teams across its key Dermatology, Respiratory, and Rhinology
Works directly with GRA Leadership, GRA personnel, as well as PMO and Finance in leading the project review process, raising issues for resolution, ensuring action items are completed, and communicating the health of both project and
