高级质量保证专员-质量管理-北京

Posted 24 Feb 2022

Beijing, Beijing - China

Req Id 241497

Details

 

A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 


Your role:

•      Personnel and Training Management

-     Personnel management: maintain and manage organization chart, personnel JD and personnel signature

-     Training Management

    Establish and maintain Training matrix

    Establish and maintain annual training plan

    Organize GDP/GSP training activities and collect training information monthly according to annual training plan, update the execution table timely

    HR4Y System: as administrator, in charge of

    Establish and maintain Training matrix

    Maintain and update training materials, personnel information in the system

    Monitor training completion status

    Coordinate and improve the courses presentation and testing paper

•      Local document management

    Responsible for document lifecycle management and the specific operation of format review, making effective and obsolete

    Maintain local document list

    Inform and follow up the related departments to perform SOP/WI periodic review

    Maintain the documents in ManGo and QA EVA page up to date

    Archive all paper documents of document lifecycle

•      Support and coordinate quality objective set up and regular review 

•      Collect the medical examination report of QA department, registry and transfer to HR

•      Establish and maintain the related SOPs and WIs for the process owned by QM group

•      Involve and support for HCQ/EQQ audit, self-inspection

•      Involve and support audit activities of supplier, distributor etc.

•      Act as backup of

    Regulation information collection and management

    Global document evaluation and implementation

•      Perform other tasks as required or assigned

 

Who you are:

EDUCATION/LANGUAGES

•      Bachelor degree or above

•      Major in pharmacy, biology, chemistry or related area

•      Good English skills

PROFESSIONAL & TECHNICAL SKILLS

•      At least 3 years working experiences in quality areas in pharmaceutical industry

•      Experience of working in QA/QC area in multinational companies is preferred

•      Good professional skills

•      Good MS office software skills (Excel, Word, Power Automate, etc.)

ADDITIONAL REQUIREMENTS

•      Good self-learning

•      Good commitment and well focus on details

•      Good communication and cross department cooperation skills

•      Be good at multi-tasking handling

 


 

What we offer:  With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

 

Curious? Apply and find more information at https://jobs.vibrantm.com

 

Apply Now