Career CategoryRegulatory Job Description Job Description Apply, obtain and maintain regulatory approvals for products within Amgen’s portfolio, including CTNs, MAAs, renewals, variations, and other life cycle management activities. Ensure all regulatory submissions are delivered on time and comply
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives
About us BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse
Background Sanofi has decided to invest into new large state-of-the art facilities for the full portfolio for insulin Drug Substances to ensure future oriented, sustainable, reliable and leading-edge long-term supply for world-wide Diabetes patients. The new
Background Sanofi has decided to invest into new large state-of-the art facilities for the full portfolio for insulin Drug Substances to ensure future oriented, sustainable, reliable and leading-edge long-term supply for world-wide Diabetes patients. The new
Background Sanofi has decided to invest into new large state-of-the art facilities for the full portfolio for insulin Drug Substances to ensure future oriented, sustainable, reliable and leading-edge long-term supply for world-wide Diabetes patients. The new
ROLE & RESPONSIBILITIES： 1. Deep understanding of customer insights Regular customer visit, frequent sales team interaction Understand the objective of different types of marketing research. Be able to identify research needs and provide clear brief to agency
Typical Accountabilities - Lead the District Team to achieve or surpass predetermined sales forecasts and call execution objectives, ensuring alignment with company sales strategies. - Collaborate with individual sales representatives to set realistic yet demanding goals
Typical Accountabilities · Ensure the optimal application of clinical pharmacokinetics (PK), pharmacodynamics (PD), and modelling & simulation (M&S) in clinical development programs, including: 1. Design and conduct clinical studies including CP studies (dosing rationales, sampling schemes,
Job Description: Details of the Division and Team Across the 21 markets we cover in Asia Pacific, Middle East & Africa, we deliver cutting-edge advisory and best-in-class solutions to the most sophisticated and demanding requirements of
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
DOCUMENT NUMBER: D001217226 TITLE:SCH.ASTINV.OPTR.I POSITION TITLE: Forklift Operator POSITIONCATEGORY: Geozone Operations REPORTS TO (JOB TITLE): DUAL REPORT Job Purpose Forkliftoperator, working under supervision operates lifting equipment requiringspecialized trade certification Roles & Responsibilities SAFETY, SECURITY & COMPLIANCE
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 aspects
Job Title: Director to Senior Director, Structural Biology Reports To: VP, Head of Discovery Unit 3 Location: Shanghai, China About Us: Structure Therapeutics develops life‐changing medicines for patients using advanced structure‐based and computational drug discovery technology.
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,
Typical Accountabilities (per AZ framework and regulatory expectations): Acting as the quality Approval / Decision maker for the GxP relevant procedure in Astrazeneca Distribution Facility. Ensure the compliance with internal Astrazeneca requirement and also relevant market Healthy
About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs
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
职位的任职者将 • 提供质量支持以实现 pMDI 项目里程碑。 • 确保青岛pMDI 项目计划在设计、施工、启动、验证（整个生命周期）期间符合 GMP 要求。 • 确保自有业务中验证计划的 GMP 合规性和运营有效性 • 与运营和质量部门的内部和外部同事进行跨职能互动，以确保完全符合 AZ 标准和当地法规。 • 支持 QA 和其他工程/运营人员以及相关技术科目的实习生，是 GMP 培训活动的主要贡献者。 • 与AZ 总部或跨职能部门合作，确保全球项目或青岛数字化、自主化项目的落地 • 根据需要支持监督和监督承包商和实习生活动 The role incumbent will • Provide Quality
Job Title: Principal Clinical Research Physician (PCRP) Job Location: China, homebased Job Overview: The PCRP, is a Medically Qualified person with extensive experience of in a drug development/drug safety environment or medical data review. PCRP independently