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- Summertime, and the Livin’ Is Easy…
- Follow-on-Biologics – More than Simple Generics
- Bacteria Versus Body Cells: A 1:1 Tie
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- Malaria – the Battle is Not Lost
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- At the Forefront in Fighting Cancer
- Molecular Motors: Think Small and yet Smaller Again…
- Liquid Biopsy: Novel Methods May Ease Cancer Detection and Therapy
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- Why Do Old Men Have Big Ears?
- The Condemned Live Longer: A Potential Paradigm Shift in Genetics
- From Research to Commerce
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Senior QMRA Specialist
Karrierelevel: Direct Entry
Anstellung: Fulltime, temporary
Start: Immediately
Standort: Seoul
Job-ID: R11174
Unternehmen: Eppendorf Korea Limited
Would you like to work for a company who has made it its mission to make a contribution to improving human living conditions? With around 5,000 employees worldwide Eppendorf is a leading Life Sciences company. We develop and distribute devices, consumables and services for use in laboratories worldwide. Our daily work is characterized by our principle: Collaborate on new ideas. You would like to take responsibility and help to make a difference in an experienced international company? Exciting tasks combined with a positive and affirmative working environment await you at Eppendorf. You are also motivated by technical challenges? Then apply now!
Your challenges
Market: South Korea, India subcontinent export market (Bangladesh, Bhutan, Nepal, Sri Lanka, Maldives), Hong Kong, Taiwan, Macao
Implement and improve a standardized and manageable MultiSite Commercial QM System for your market which will reduce the complexity and duplication of activities across Sales and Service Organizations while building capabilities to:
- Ensure compliance to enable growth
- Drive continuous improvement and deployment
- Focus on prevention action and customer satisfaction
Manage the design of end-to-end quality processes and tools to achieve highest customer satisfaction
Drive process harmonization and standardization within your market in alignment with Corporate QM
Be Management Representative for your market (according to local QM System)
Be first contact partner for the complaint management process for your market
Ensure correctness of complaint data entry for your market
Liase with Eppendorf SE in case of adverse event reporting and field safety corrective action
Overview and support all RA aspects as needed, incl. required registrations and certifications
Gather, analyze, assess, and communicate regulatory requirements and be internal and external contact point for market-related regulatory inquiries for your market
Liase with Corporate RA and R&D RA to identify market requirements and for submission in your market
Lead development and roll out of QM, PMS, and RA KPIs for area and processes of responsibility
Implement and maintain the effectiveness of the MultiSite Commercial QM System and ensure compliance with applicable standards for your market
Define, design, and utilize QM practices and tools
Implement and improve quality processes in alignment with Corporate QM
Design end-to-end processes as iniative leader
Organize and conduct document control, change management, management review, audit, nonconformance, and CAPA management
Provide QM related trainings within your market
Represent the your market as Management Representative
Communication and first contact partner for the complaint management process
Review uniformity of complaint registrations, incl. data cleaning and correction (Quality Review)
Conduct with complaint classification trainings to support training, mentoring, and continuous improvment
Monitor local adverse event reporting, and field safety corrective action
Represent your market torwards notified bodies and regulatory authorities
Proactively screen for new and relevant local regulatory requirements and standards for markets managed
Assess local regulatory requirements and provide information for Eppendorf impact
Liase with Corporate RA and R&D RA to identify market requirements for submission
Process QM/RA realted customer inquiries
Build KPIs and monitor QM, PMS, and RA KPIs, thereby collect data and provide reports
Support other QMRA colleagues in the region as required
Your expertise
Quality Systems Expertise: Deep knowledge in Q-Systems, specifically ISO 9001, ISO 17025, and ISO 13485.
Regulatory Knowledge: Extensive experience in regulatory submission processes in Korea.
Industry Experience: At least 3 years of experience in the Life Science or Medical Device industry.
Educational Background: Degree in natural sciences or a comparable scientific or technical education.
Skills & Competencies:
Excellent English language and communication skills; additional language skills related to relevant markets are desirable.
Intercultural Competence: Strong intercultural competence with experience working with Asian and European/Western organizations.
Collaborative Skills: Proven ability to work cross-functionally in a matrix organization.
Communication: Exceptional communication skills, capable of leading and influencing at all organizational levels.
Your benefits at Eppendorf:
We truly appreciate our employees and their performance
We offer a wide range of learning and development opportunities to allow you to deepen your technical knowledge and for continuous growth
By working with us, you will make a meaningful contribution to improving human living conditions
Attractive salary, employee benefits and performance bonus
Note: This recruitment is for a fixed-term leave replacement; the contract term is 17 months, with the possibility of renewal.
Bitte beachten Sie, dass wir grundsätzlich nur Bewerbungen berücksichtigen, die online über unser Bewerbermanagementsystem eingehen.
Wir freuen uns, Sie kennenzulernen!
Bei weiteren Fragen wenden Sie sich bitte an
MEOR HARITH ALWY MEOR SHAMSHUL ANUAR,
Eppendorf. Collaborate on new ideas.