苏州招聘

POSITION SUMMARY           

  

•       This position reports to the VP Global Quality.  The APAC Quality Platform Leader (QPL) will have overall responsibility to assure quality objectives are met by internal (GMS) manufacturing organizations and will be the Senior most Zoetis Quality member of management in the Region.   The QPL will have direct reports (i.e. site QO leaders at GMS sites) and will serve as a partner alongside other stakeholders (e.g. VMRD, VMRA, GMT and Commercial colleagues) to enable business objectives by meeting the quality objectives.

   

•       The Region has several Zoetis manufacturing sites – consisting primarily of Medicated Feed (MFA) and Biologics technologies that the APAC Quality Platform Leader has responsibilities. Networking with the other Quality Platform Leaders – especially the MFA and Bios Leaders – is critical to maintain continuity and alignment for the application of Zoetis Quality Management System. 

    

•       The APAC Quality Platform Leader will develop longer term Quality Strategy objectives and Quality Roadmaps to keep the Platform compliant with applicable quality regulations, maintain agility, and ensure effectiveness across the Business.

    

•       The Leader will establish/maintain appropriate processes and metrics to manage the platform and enhance problem solving at all levels of the quality organization.  Quality Council partnership with Operations Leadership is essential to realizing the overall Quality Culture for the Business.

  

POSITION RESPONSIBILITIES   ·        

  

•       Serve as a quality culture role model, and promoting a strong Quality & Compliance culture across the APAC Platform that translates into a First-Time-Right mind-set in the network.
•       Insure Quality System Standards and Processes are appropriate and up to date for the platform.
•       Develop long-term Quality strategy for theTechnology Platform operations
•       Organizational Goals translated/adapted to Technology Platform goals
•       Management of Platform Process Goals as well as the QMS.
•       Creation / Management of the Quality Roadmap for the Technology Platform and assist sites in their Roadmap Development
•       Lead strategic and tactical deployment of problem solving and other methodologies leading to continuous improvements across Technology Platform sites, including lean lab deployment. Monitoring CAPA effectiveness at each respective sites
•       Assuring the use of operational excellences tools in quality processes
•       Establish and Lead the Quality Governance Council for the Technology platform, to inform management about product quality and process performance, quality risks, compliance with internal and external requirements.
•       Use trended metrics and audit data to drive site initiatives for increased performance
•       Develop and Manage the reporting applicable metrics for the Technology Platform
•       Maintain linkage to Surveillance and Audit services to fully evaluate the Sites’ regulatory compliance position
•       Understand  Key Points of Compliance (KPCs),Standards, and Processes specific to the Platfo
•       Oversee Capital Investment requests at site levels to drive quality and compliance

    

Staff and Leadership Responsibilities

•       Leadership Development / Coaching of Staff; Creation of Learning Organization
•       Stewardship of the Quality Culture within the QA Function as well as the Site.
•       Insure Training and Development plans are in place for all Quality associates (QA and QC) of the APAC platform.
•       Development of APAC Platform Quality operations budget and resource planning for roll up to the Site Quality Budget.
•       Support the development of Quality goals and targets as part of the organisation’s strategic plan.

  

 

ORGANIZATIONAL RELATIONSHIPS   ·     

•       Manufacturing Operations
•       Corporate Compliance/Audit Group
•       Manufacturing GMT
•       VMR&D
•       GSS
•       GMS Functional Operations (ie: HR; Procuement; GES etc)
•       VMRA
•       SCQO
•       Commercial Operations
•       Manufacturing IT

    

RESOURCES MANAGED 

Financial Accountability        

•        Annual Operating Budget anticipated: $ 3-5 Mio

Supervision  

•       The role will give direct supervision to 5-7 Quality Managers
•       Highly matrixed organization; Influence without authority necessary

    

EDUCATION AND EXPERIENCE

•       Science or Engineering Bachelors / Masters Degree
•       Significant Operations and/or Quality experience (10+ years) in Animal Health/Human Health manufacturing
•       Previous Leadership experience
•       Demonstrated ability to operate successfully in a matrix organization
•       Fluency with ICH Q10 Preferred
•       Six Sigma Black Belt / Green Belt or Lean Practioner Preferred
•       Experience in working with FDA, EU, Chinese regulations.

    

TECHNICAL SKILLS REQUIREMENTS

•       People Management / Demonstrated Leadership Skills
•       Demonstrated success in a Quality Operations Role
•       Sets Clear Direction and Aligns Team and Others Around Common Objectives
•       Ability to develop and build a strong leadership team at the sites which can support the business
•       Ability to develop and adhere to self-directed standard work.
•       Ability to analyze data and synthesize to make data driven decisions 
•       Ability to Develop and Implement Strategic Initiatives
•       Business Acuumen
•       Process Owner Management
•       Change Agent; Passion to win and can be successful in managing a change environment
•       Continuous Improvement and break-thru thinking
•       Fluency in English and Chinese

    

PHYSICAL POSITION REQUIREMENTS

•       Singapore or Shanghai based office position
•       Position requires flexible work hours, to accommodate varying teams and markets’ time zones
•       This position will require fluent use of teleconferencing and Webex tools, as well as Sharepoint technologies, to share and manage information with global locations and manufacturing sites
•       Travel: Estimated 30% global travel

    

ACRONYM DEFINITIONS

•       QSS: Quality Systems and Standards
•       QA: Quality Assurance
•       QC: Quality Control
•       ESQA: External Supply Quality Assurance
•       SC QO: Supply Chain Quality Operations
•       GMS: Global Manufacturing and Supply
•       VMRA: Veterinary Medicine Regulatory Affairs

  

 

  

About Zoetis
Zoetis is a global animal health company dedicated to supporting customers and their businesses in ever better ways. Building on 60 years of experience, we deliver quality medicines and vaccines, complemented by diagnostic products, genetic tests, biodevices and a range of services. We are working every day to better understand and address the real-world challenges faced by those who raise and care for animals.
Why Zoetis
Zoetis has more than 60 years of experience in delivering innovative, high-quality products and services that benefit our customers.
Zoetis work environment
At Zoetis, we take pride in a collaborative spirit and high-performing environment where every colleague is given room to learn and grow.
Your opportunities at Zoetis
We invest in our people and offer diverse and exciting opportunities to make a difference in a growing global industry while shaping the future of animal health.
Results that matter
Our colleagues make an impact by working hand-in-hand with those who raise and care for animals to better understand and address the unique real-world challenges they face.



硕腾，原为辉瑞的动物保健部门，作为一家全球领先的动物保健公司，致力于为客户及其业务提供最有力的支持。秉承60年的悠久历史，我们为用户提供优质的兽药和疫苗、业务支持和技术培训。

在《福布斯》“2017年美国***雇主（中型企业）”中硕腾公司也有幸入选，这是硕腾公司第二年入选，排名在Top300中列114位。这份殊荣是对硕腾的工作环境、公司文化和企业品牌的认可。我们将继续不懈努力，帮助饲养和关爱动物的人们，为他们解决所面临的各种挑战。

我们的英文名字Zoetis (zō-EH-tis)，其词根为zo，以 zoo（动物园）和zoology（动物学）而广为人知。Zoetis源于zoetic（有生命的，有生气的），蕴含“赋予生命的意义”之义。硕腾（Zoetis）致力于为世界各地的饲养和关爱动物的兽医和畜牧从业人员提供支持。