logo
更新:2024-03-24
APAC Process / Quality Analyst
7-9千
大连甘井子区  | 1-3年  | 本科  | 社招
已结束
职位详情
ROLE SUMMARY

The Meetings, External Engagements, & Travel (MEET) Process / Quality Analyst
will support the Regional Process Integration & Controls Manager in
implementing MEET processes and overseeing adherence to processes, policies,
controls, and standards within APAC. The Regional Process / Quality Analyst
will be responsible for transaction sampling and system reviews to ensure
processes and systems functionality. Additionally, this Analyst will play a
central role in addressing escalations, exceptions, and deviations related to
MEET processes.
This Analyst will demonstrate accountability and integrity in the face of
challenge and respond to change with agility, optimism, and innovation. They
will collaborate cross-functionally as appropriate.  
This role will be based in Dalian, China and work with other Process / Quality
Analysts, regional operations team, regional HCP payments team, regional
sourcing team, and other COEs as appropriate. The Process Analyst will report
directly to the Process Integration and Controls Lead Manager for APAC.

*
Support the resolution of escalations; exceptions; and deviations related to
MEET transactions and processes within APAC

*
Ensure all escalations; exceptions; and deviations are documented

*
Work with regional Process Integration & Controls Manager to identify
opportunities for process changes that will better balance compliance needs
with business operational goals

*
Serve as first point of contact for compliance-related questions for MEET
transactions and processes

*
Support a review of data trends to identify risk areas and work closely with
Legal, Compliance and Audit to solution gaps

*
Work with Anti-Corruption Program Office and Compliance to ensure MAPP
transactions comply with MAPP policy and other healthcare professional
policies; review control design for any enhancements and ensure proper standard
operating procedures are in place

*
Conduct periodic quality reviews of MEET systems to ensure standard controls
are functioning as expected

*
Conduct detailed review/submission of a monthly audit sampling of My
Anti-Corruption Policy and Procedures (MAPP) transactions to ensure accuracy

*
Conduct detailed monthly reviews of selected meetings (via sampling) to ensure
adherence to MEET processes

*
Support the development and delivery of training aimed at addressing key
findings identified via monthly MAPP/MEET sampling

*
Ensure all transactions are properly documented in applicable MEET system and
ensure standards are in place

*
Support audit preparation and execution

*
Ability to present to leadership and manage relationships with stakeholders

*
Support Regional Process Integration & Controls Manager in working with
ACPO/Compliance to manage approvals for exceptions and identify opportunities
for further simplification of MEET processes and controls to better align with
business operational goals (while still maintaining a strong compliance posture)

*
Support trainings related to MEET policies and processes as needed

*
Support regional lead in raising compliance questions and challenges to
Corporate Compliance and / or Audit through regular governance meetings

*
Raise compliance questions and challenges to Corporate Compliance and / or
Audit through regular governance meetings
BASIC QUALIFICATIONS

*
Comprehensive knowledge and expertise in the technology landscape that
supports MEET 

*
Experience with accounting or compliance / audit transactions, preferably in a
shared service with strong compliance controls

*
Ability to manage multiple stakeholders

*
Proficiency in PC skills (MS Excel, Word, PowerPoint) required

*
Good organizational skills to coordinate and manage multiple priorities

*
Strong technical skills in managing transactions within a system

*
Strong written and verbal communication skills enabling effective
communication with all levels of management

*
Strong customer service skills and mindset

*
Understanding of accounting terms and financial cycle

*
Understanding of compliance / financial controls

*
Strength with multitasking and ensuring accurate detail

*
Ability to work under pressure and to handle several projects at once

*
High level of self-motivation, energy and flexibility

*
Understanding of MAPP Policy terms and healthcare compliance policies

*
Strong interpersonal and organizational skills
PREFERRED QUALIFICATIONS

*
Typical Years of Experience: Less than 2 years of experience in management,
compliance, and customer focused operations with significant volumes and risk
(including audit and/or finance experience)

*
Minimum of bachelor’s degree in Business, Finance, or a related discipline

*
Fluency in English and Chinese is a must; additional languages preferred

*
Compliance experience and financial or audit controls background

*
Comfort with ambiguity, anticipates changes, and influences direction of
innovative operational strategies

*
Previous experience with pharmaceutical companies is preferred

*
Fundamental knowledge of a large compliance related, customer facing
operations team

*
Ability to engage with stakeholders to resolve issues and achieve objectives

*
Proficiency in PC skills (MS Excel, Word, PowerPoint) required

*
Proficiency with data analysis and visualization

*
Experience with accounting or compliance / audit transactions, preferably in a
shared service with strong compliance controls

*
Experience with Foreign Corrupt Practices Act transactions preferred
PHYSICAL/MENTAL REQUIREMENTS

Position is located is Dalian, China. Travel would be for work related needs
only. Weekend work could be necessary based on volumes.
 
Work Location Assignment: Flexible
Pfizer is an equal opportunity employer and complies with all applicable equal
employment opportunity legislation in each jurisdiction in which it operates.

Global Procurement
#LI-PFE

其他信息

行业要求:全部行业
工作地址
大连-甘井子区海创大厦C栋
公司介绍
辉瑞公司(Pfizer Inc.)创建于1849年,总部位于美国纽约,是一家以科学为基础的、创新的、以患者为先的生物制药公司。辉瑞的使命是“为患者带来改变其生活的突破创新”。
在辉瑞,我们通过科学和全球资源为人们提供治疗方案,以延长其生命,显著改善其生活。在医疗卫生产品的探索、研发和生产过程中,辉瑞始终致力于奉行严格的质量、安全和价值标准。
我们在全球的产品组合包括创新药品和疫苗。每天,辉瑞在发达和新兴市场的员工都在推进人类健康,推动疾病的预防、治疗和治愈,以应对挑战我们这个时代的顽疾。
辉瑞还与医疗卫生服务方、政府和社区合作,支持并促进世界各地的人们能够获得更为可靠和可承付的医疗卫生服务。这与辉瑞作为一家全球卓越的创新生物制药公司的责任是一致的。170余年来,辉瑞一直致力于为所有依赖我们的人带来改变。
辉瑞于1989年进入中国市场。扎根中国30余年,辉瑞已成为在华主要的外资制药公司之一。2021年是辉瑞新征程的开始。迄今已有170余年历史的辉瑞正在迈入全新时代,成为一家以科学为基础的、创新的、以患者为先的生物制药公司。目前辉瑞在中国业务覆盖全国300余个城市,累计投资超过15亿美元,并设立了1家先进的生产设施,2个研发中心(分别位于上海张江高科技园区和武汉光谷),在华有近7,000名员工分布于业务、研发和生产等领域。辉瑞在华上市了五大领域的高品质创新产品,包括肿瘤、疫苗、抗感染、炎症与免疫、罕见病等多个领域的处方药和疫苗,强大完善的产品线旨在满足生命各阶段的健康需求。
多年来,辉瑞始终致力于“成为中国医疗卫生体系重要组成部分”,运用全球医疗资源,与社会各界合作,积极推进中国健康事业。未来,辉瑞将继续践行“为患者带来改变其生活的突破创新”的使命,秉承“科学致胜”的理念,以创新为动能,与中国政府部门和社会各界合作,积极引进突破性的创新药物,探索药物可及性创新方案,及时惠及中国患者,助力“健康中国2030”宏伟目标的实现!
若用人单位提供虚假招聘信息,以担保或其他任何名义收取财物,扣押或以保管为名索要证件,都属于违法行为,应当提高警惕。
发布于