דרושים District & Manager ב-Msd ב-China, Huairou District

Job Description

Position Objective

Duties and Responsibilities

• Identify innovative assets from academic institutes, research centers and industry.
• Participate in external project evaluation, collect and analyze information on specific topics related to project of interest to support evaluation, and responding to special due diligence request.
• Write formal reports and prepare presentation materials, such as project evaluation reports, project progress update reports, due diligence reports, data summary presentation, project update presentation etc.
• Generate knowledge graph for disease-indication-therapeutic target
• Analyze scientific literatures on disease and target MOA and related preclinical and clinical data, generate insights on unmet medical needs, critical challenges, emerging development trends, key benchmarks for new drug development, etc.
• Conduct primary research due diligence on indications / targets / technologies of interest, conduct deep dive comparisons on current and emerging treatment options, and identify pipelines to be prioritized as benchmarks, and write comprehensive research reports.
• Monitor scientific and industry progress and update the reports with newly emerging insights periodically.

Key Requirement

Education and background:M.D. in Medicine or Ph.D. in Biology

3-8 years of work experience in assets evaluation, literature research or competitive intelligence of pharmaceutical R&D. Medical training preferred. Previous roles in biotech-focused consulting, biotech equity research, biotech investment analyst with experience in asset-level scientific diligence preferred.

Skills:

• Knowledge of innovations/assets in academic and translational research center
• Strong information search & collection capability, proficient skills in using commercial & public database and various other sources.
• Sharp analytical skills in dissecting preclinical and clinical data with rigorous attention to detail
• Excellent written and verbal communication & presentation skills in Chinese and English.
• High proficiency in writing and formatting reports and presentation, proficient skills in using Microsoft Office tools

Current Contingent Workers apply

No Travel Required

Not ApplicableNot Indicated

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

• Work allocation, staff development and performance appraisal.
• Provides input for capacity planning, including reporting of current manpower and forecasting
of CRA capacity and needs, to provide efficient use of resources.
• Work with CRAs, PLMS and other functions to ensure consistency of processes and protocol
implementation across the country, to reduce variability and provide predictability.
• Interacts with sites as needed to resolve site or CRA operational issues to meet• Attend local Investigator Meetings if requested to.
• Interface with partners in the Clinical Operation Department on clinical trial execution.
• Escalates site performance issues to the CRM and Clinical Research Director CRD.
• People and Resource Management:
o Manage CRA – career development, performance reviews, etc., including
addressing low performance situations and taking appropriate actions.
o Support and resolve escalation of issues from CRAs.
o Liaise with local HR and finance functions as required.o Provides training, support, and mentoring to the CRA to ensure continuous
development.
o Ensures CRA compliance with corporate policies, procedures, and quality standards

• Ability to work independently and in a team environment
• Excellent people management, time management, project management and organizational skills
• History of strong performance
• Skills and judgment required to be a good steward/decision maker for the company
• Fluent in the Local Language and business proficient in English (verbal and written)
• Excellent working knowledge of all applicable ICH/GCP regulations and Good
Documentation Practices and the ability to work within these guidelines
• Expertise in and excellent working knowledge of core trial management systems and tools

• High emotional intelligence
• Strong leadership skills with proven success in people management
• Excellent interpersonal and communication skills, conflict management
• Demonstrated ability to build relationships and to communicate effectively with external
customers (e.g. sites and investigators)
• Influencing skills

• Minimum of 5 years´ experience in Clinical Research
• Minimum of 3 years’ experience as CRA monitoring clinical trials
• Line management experience preferred or, at least team leader experience

• Bachelor’s degree in Science

• Advanced degree (e.g. BA/BS or higher) with a strong emphasis in science and/or biology

Current Contingent Workers apply

Not ApplicableNot Indicated

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

Brief Description of Position

Manage registered products and support product registration projects within the team aligned timeline.

• Communicate with international RA
• Provide RA input on the strategic planning for all responsible products
• Prepare registration dossiers and questions following related regulations and procedures
• Make good relationship with officials
• Make good relationship with experts
• Organize the registration evaluation meeting
• Coordinate Q.C. re-confirmation test with institute for drug control
• Obtain final registration permits

Qualifications, Skills & Experience

• Bachelor and above in medicine, pharmacy or related disciplines
• Minimum 6 years working experience in pharmaceutical industry
• Over 5 years’ experience in registration field
• Proficiency in the use of EXCEL, POWERPOINT and WORD
• Good command in English, both in written and spoken
• Proactive and teamwork spirits

Current Contingent Workers apply

Not ApplicableNot Indicated

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

We are currently seeking a Quality Specialist to join our biotech facility. As a Quality Specialist you will provide direct quality support to a production area as part of a Quality IPT (Integrated Product Team). The Quality Specialist ensures quality and compliance of products manufactured by the functional area, adherence to Good Manufacturing and Documentation Practices, and represents quality. You will work as part of a shift roster (days role) 4 days on/4 days on

What you will do:

Bring energy, knowledge, innovation, and leadership to carry out the following:

• Responsible for review/approval of new and updated Master Batch Records / Electronic Batch Records
• Review and approve production documentation such as executed electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures
• Review and approve new and updated SOPs/ Work Instructions and Controlled Job Aids
• Actively participates in the Tier process and use this forum to make issues visible and to partner with the functional area on resolution
• QA support, review and approval of Commissioning and Qualification lifecycle documents for capital projects and new equipment.
• Serve as the Quality SME for Performance qualification (PQ) activities across the site including but not limited to: Equipment, Facility and Utility PQ studies, Cleaning Validation, SIP, process validation when required.
• Participate as the quality member on cross functional projects
• Support sustaining activities such as Change Management, Deviations, CAPAs, Equipment Requalification and Periodic review, Site Maintenance & Calibration Program
• Provides support to internal audits and regulatory inspections
• Coach and guide colleagues to ensure documentation is completed right first time, and to ensure compliance with cGMPs and regulatory requirements
• Collaborate with cross-functional team members in the identification and implementation of continuous improvement initiatives and action plans
• Drive continuous improvement and utilise problem solving tools and MPS (Our Company Production Systems) Participate in continuous improvement initiatives to enhance operational efficiency and resolve issues

In order to excel in this role, you will more than likely have:

• Bachelor’s degree (or higher) in Engineering, Chemistry, Biology, or relevant discipline.
• Minimum 5 years of relevant experience in GMP Manufacturing, Quality Assurance or Laboratory environment, Pharmaceutical/Biological Quality, Operations, Technical, or Regulatory function supporting manufacturing or laboratory operations.
• Understanding of QA operations is an advantage
• Evidence of leadership skills coupled with excellent and written communication skills
• Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work in a team environment

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,please apply today.

Current Contingent Workers apply

Not Applicable

Adaptability, Adaptability, Aseptic Manufacturing, Biopharmaceutical Industry, Capital Projects, cGMP Compliance, Change Management, Data Analysis, Data Integrity, Decision Making, Documentation Review, FDA Regulations, GMP Compliance, Interpersonal Relationships, Laboratory Operations, Laboratory Quality Control, Management Process, New Product Development, New Product Introduction Process, Operational Efficiency, Pharmaceutical Process Engineering, Quality Assurance (QA), Quality Inspections, Quality Management, Quality Operations {+ 4 more}

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

2. 合理管理、使用并整合市场资源，洞悉并把握市场机会，提高资源有效性

3. 联合市场部，医学部及ACE等跨部门团队和经销商团队重点推进在大区层面的重点项目有效落地

4. 掌握并熟悉领域专业知识，并赋能大区销售团队和经销商团队

5. 培养全国/区域讲者及KOL，主动搭建学术平台

医药相关专业本科学历及以上，5年以上医药行业经验，具有市场或销售管理经验；疫苗行业经验优先； 具备良好的数据分析和逻辑思维，能够将客户和市场洞见转化为大区市场策略和计划 良好的合作影响力，能够与内外部关键决策者互动，主动担当，具有良好的学习能力和适应性

Current Contingent Workers apply

Not Applicable

Adaptability, Adaptability, Agile Methodology, Animal Health Sales, Business Strategies, Clinical Documentation, Creative Campaign Development, Customer Service, Data Analysis, Emergency Care, Hospital Medicine, Immunizations, Interpersonal Relationships, Logical Thinking, Management Process, Marketing Budget Management, Marketing Data Analysis, Marketing Strategies, Marketing Strategy Implementation, Market Research, Nursing, Pricing Strategies, Product Lifecycle Management (PLM), Project Management, Sales Management {+ 5 more}

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

在指定的区域内, 达到指定产品的目标，市场占有率和增长率,并有效地利用资源和控制费用

确保在产品推广和日常工作中, 严格遵守公司的各项SOP和财务制度，确保自己的行为符合公司的道德准则和原则

与同事分享、交流信息, 互相帮助, 使个人和团队共同发展

岗位技能：产品及市场知识 ；产品推广技巧及流程；区域管理；业务的敏锐性；辅导他人

Current Contingent Workers apply

Not Applicable

Accountability, Accountability, Account Management, Adaptability, China Strategy, Consumer Healthcare, Customer Relationship Management (CRM), Customer Service, Data Analysis, Drug Information, Health Information Management, Information Collection, Interpersonal Relationships, Lead Generation, Management Process, Market Analysis, Medicinal Chemistry, Oncology Sales, Order Processing, Pharmaceutical Guidelines, Pharmaceutical Management, Product Knowledge, Revenue Generation, Sales Forecasting, Sales Reporting {+ 1 more}

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

Job Description

Brief Description of the Position

Manage registered products and support/lead groups to register new products as soon as possible.

• Communicate with international RA
• Provide RA input on the strategic planning for all responsible products
• Manage registration dossiers preparation following related regulations and procedures
• Make good relationships with officials
• Make good relationships with experts
• Organize the registration evaluation meeting
• Coordinate Q.C. re-confirmation test with the Institute for Drug Control
• Obtain final registration permits

Qualifications, Skills & Experience

• Bachelor and above in medicine, pharmacy, or related disciplines
• Minimum 10 years of working experience in the pharmaceutical industry
• Over 8 years experience in the registration field
• Proficiency in the use of EXCEL, POWERPOINT and WORD
• Good interpersonal communication skills
• Good command of English, both in written and spoken
• Demonstrated leadership and credibility

Current Contingent Workers apply

Not ApplicableNot Indicated

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.