黄山 [切换城市] 黄山招聘黄山市场/营销招聘黄山市场/营销/拓展主管招聘

Submissions Team Leader(职位编号:963159_1332409541)

惠氏制药有限公司

  • 公司规模:500-1000人
  • 公司性质:外资(欧美)
  • 公司行业:制药/生物工程

职位信息

  • 发布日期:2012-11-13
  • 工作地点:上海
  • 招聘人数:1
  • 工作经验:二年以上
  • 学历要求:本科
  • 语言要求:普通话熟练
  • 职位类别:市场/营销/拓展主管  Helpdesk 技术支持

职位描述

Role Description
ob Posting
招 聘 通 知
There's a new opening for Pfizer China R&D Centre based in Shanghai, reporting to Submission Publishing Leader. Please refer to the job description as following:

Position: Submissions Team Leader (Contractor, hire through CIIC)
Department: WSRO, Submissions & Product Licensing Support (S&PLS)
Report to: Submission Publishing Lead
Career Ladder Level / Grade: Manager / Senior Manager
Location: Shanghai, China

Position Summary:
*To manage submission publishing activities at the regional level ensuring that Pfizer delivers on key regulatory submission milestones and maintains compliance with applicable regulatory obligations.
*At time of peak load across the organization, the incumbent is expected to publish submissions, and at all times will have comprehensive and detailed oversight of quality control and regulatory workload within their function.

Resources Managed (budget and FTEs):
*Direct Management responsibility for local submission specialists (or equivalent contracted resource), with responsibility for publishing regulatory submissions at designated location.
*Local and remote peers, external/internal customers and business partners associated with development, build and delivery of human health submissions.
*Internal liaison will include Worldwide Regulatory Strategy, supplier groups across Clinical, Medical, Commercial and Informatics.
*External liaison may include Licensing/Marketing Partners, Regulatory Authorities, and Industry Associations

Primary Duties:
Ensuring successful portfolio delivery to designated health authorities to agreed time and quality standards. Managing the resources associated with compilation, publishing and delivery of all marketing applications that support new development projects and maintain regulatory compliance for investigational new drug applications and existing marketed product applications.

Key Accountabilities:

*Direct and active supervision of a subgroup within Submissions, specifically focused on a subsection of the portfolio or type of specialist support to the business.
*Proactive liaison with remote customers within designated region to ensure streamlined product delivery
*Coordinates with remote/local peers to ensure compliance with local and global regulatory requirements
*Ensures that assigned projects/technologies relating to evolution of submission build, publishing and delivery processes and deliverables are carried out according to timelines
*Coordinates load balancing and resources at the respective site and in support of remote sites
*Develops ideas seeking efficiencies and effectiveness while managing the submissions portfolio
*Responsible for professional development through mentorship and motivation

Training & Education Requirements:
*Master or undergraduate degree in biological, pharmaceutical, or medical sciences preferred
*Training or experience in team management preferred
*Training or experience in regulatory submissions preferred
*Training or experience in project management preferred

Experience Requirements:
*Proven aptitude in project management and process redesign
*Articulate with strong analytical and interpersonal skills
*Ability to successfully establish and build collaborative relationships with colleagues throughout Submissions and across the organization
*Functions as a change agent that can exhibit regulatory knowledge and awareness, technical competence, sound judgment, and a professional demeanor
*Demonstrates leadership and flexibility in dealing with change and diversity
*In addition, relevant experience includes a proven ability to work successfully on global teams
*Experience in regulatory affairs and significant knowledge of submissions processes.

Competency Requirements:
*Excellent command of English, written and verbal, able to communicate effectively with colleagues and stakeholders
*Good understanding of regulatory requirements
*Demonstrate time management and project management skills for successful milestone / timeline achievement
*Strong organizational and planning skills in order to meet timeline requirements and to handle multiple projects whilst showing prioritizing skills
*Ability to work effectively in a multi-cultural context and matrix organization
*High teamwork spirit
*Able to act due to time zone distance
*Participates in appropriate training pertinent to performance

公司介绍

GSK is an equal/opportunity affirmative action employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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联系方式

  • Email:chk.recruitment@gsk.com
  • 公司地址:地址:span东莞