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Job Mission
Represent manufacturing and act as gatekeeper from manufacturing to D&E function
Add value in overall manufacturing processes such as forming, machining, joining, and assembling
Job Description
Contribute to the solution of faults and takes the necessary initiatives and practical decisions to ensure zero repeat
Identify gaps and drive assigned process improvement projects and successful delivery
Initiate and drive new procedure changes and projects
Develop and maintain networks across several functional stakeholders
Prioritize works and projects based on business situation
Transfer knowledge and train colleagues on existing and newly introduced products
Education
Master degree in technical domain (e.g. electrical engineering, mechanical engineering, mechatronics)
Experience
3-5 years working experience in design engineering
Personal skills
Show responsibility for the result of work
Show proactive attitude and willing to take initiative
Drive for continuous improvement
Able to think outside of standard processes
Able to work independently
Able to co-work with different functional stakeholders
Able to demonstrate leadership skills
Able to work in a multi-disciplinary team within a high tech(proto) environment
Able to think and act within general policies across department levels
Diversity and inclusion
ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that diversity and inclusion is a driving force in the success of our company.
Need to know more about applying for a job at ASML? Read our frequently asked questions.
Introduction to the job
Do you like challenges and do you want to work in a fast pacing supply chain environment to support some of the biggest semiconductor companies worldwide? Are you familiar with Logistics Operations and like to managing urgent demands on a daily basis?
If this sounds like you and if you have a strong customer oriented mindset, here is your mission.
Role and responsibilities
For our Global Operations Center in Taiwan we are searching for Supply Chain Professionals. You fulfill the demand of our customers for spare parts and tools for their maintenance activities on some of the most complex machines in the right quantity and at the right time & cost.
Time is of the essence to ensure a seamless production of our customers without interruptions on our machines.
-Handling of urgent material requests from worldwide customers in a rolling 24/7 shift system with the right customer focus, while meeting all milestones related to communication and execution
-Monitoring of worldwide shipments
-Ability to resolve complex issues and drive improvements to further optimize processes
-Ability to support escalations and provide communication proposals for review
-Constructive and reliable communication with worldwide stakeholders from all departments within ASML
-This position requires shift work.
Education and Experience
Bachelor's Degree in related subject i.e. Supply Chain Management, Information Science, Engineering etc. preferred
-Minimum 1 year of relevant experience in an international company, semiconductor industry is preferred
-A tactical thinker with strong interpersonal and communication skills
-Analytical thinking and ability to organize and prioritize workload
Skills
Working at the cutting edge of tech, you’ll always have new challenges and new problems to solve – and working together is the only way to do that. You won’t work in a silo. Instead, you’ll be part of a creative, dynamic work environment where you’ll collaborate with supportive colleagues.
There is always space for creative and unique points of view. You’ll have the flexibility and trust to choose how best to tackle tasks and solve problems.
To thrive in this job, you’ll need the following skills:
-Stress-resistant; act under high pressure
-Flexible; willing to go the extra mile for the customer
-Excellent professional communication in English, written and oral
-Drive for results; does not stop until solution has been found, even when obstacles arise
-Team player
-Change management competencies
-Convincing, pro-active and “can do” mentality
-Cultural awareness
-Experience with ERP system(s), SAP R/3 knowledge preferred
-Ability to prioritize
Diversity and inclusion
ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that diversity and inclusion is a driving force in the success of our company.
Need to know more about applying for a job at ASML? Read our frequently asked questions.
CerbACT Asia provides testing services for both global and local clinical trials. As a perspective member of the Flow Cytometry Department, you are expected to perform routine flow cytometry testing, PBMC isolation, and cell culture, as applicable. You are also responsible for the maintenance of flow cytometers, cell counters, and other related instruments and equipment. You will be working under regulations of the College of American Pathologists (the CAP) and guidelines of the Good Clinical Laboratory Practices (the GCLP) under supervision of Scientist and Department Head.
As a member of our team, you will have the opportunity to collaborate with our partner labs in the EU and the US. You will participate in assay transfer validations for cutting-edge flow cytometric assays, fostering your professional development.
Responsibilities:
- Perform routine lab testing including flow cytometry, PBMC isolation, whole blood pelleting, (ultra)centrifugation, and cell culture, as applicable.
- Maintain test results and all related records.
- Analyze flow cytometry test results and draft test reports, as applicable.
- Schedule maintenance of lab instruments.
- Perform incoming material QC of antibodies, including inter-lot and inter-shipment comparisons.
- Assist in maintaining adequate laboratory supplies.
- Document all tasks performed according to company’s Quality Management System (QMS) and policies.
- Participate in regular meetings and discussions and present data internally.
- Revise SOPs to improve the workflow.
- Any other department tasks assigned by supervisor.
CerbACT Asia 為全球和台灣當地臨床試驗提供測試服務。 作為流式細胞技術部門的正式成員,您需要執行常規流式細胞儀測試、PBMC 分離和細胞培養(如果適用)。 您也負責流式細胞儀、細胞計數器以及其他相關儀器和設備的維護。 您將在研究員和部門主管的監督下,按照美國病理學家學會 (CAP) 的規定和優良臨床實驗室規範 (GCLP) 的指南之下進行工作。
作為我們團隊的一員,您有機會與我們在歐盟和美國的合作夥伴實驗室合作。 您將參與尖端流式細胞儀檢測的檢測轉移驗證,以促進您的專業發展。
Responsibilities:
Leading strategy development and execution within disease area
• Participate actively and ensure appropriate input based on strategic insight and scientific expertise in the respective Brand Teams
Demonstrate broad strategic thinking and planning by developing objectives, plans and actions that are effectively addressing our organizational strategy and customer needs: Ensure country medical activities are in line with approved medical strategies
Ensure country clinical trials and studies are delivered to agreed standards of time, quality and cost as well as an appropriate participation in international trials
Identify and follow up Post Marketing Trials and coordinate budget for own country/cluster
Manage/coordinate Disease Area medical budget for own country/cluster and liaise, as appropriate, with Finance and Purchasing
Liaise with Medical Director to manage unexpected events or issues such as the early close of a study at country level
Build country/cluster reputation and visibility of medical team at the international level by managing the timely execution of trials and other medical activities
Proactively provide scientific support to Commercial, Regulatory, Market Access, Outcomes Research, Pharmacovigilance and Legal Counsel
• Coordinate the medical plan processes for the Disease Area in alignment with the appropriate local/cluster functions (including Commercial, Regulatory, Market Access, PV and Outcomes Research) and with the appropriate international Medical Teams (WW/EMAC/IC)
Requirements:
Preferred Experience & Knowledge
• Extensive experience working in cross-functional teams
• Extensive experience in designing and managing clinical trials across different phases of development and resolving clinical trial-related issues
• Track record in effectively managing risk and compliance
• Building strong relationships with External Experts within DA
• Experience in developing medical plans aligned with overall disease & product objectives
• Experience in developing, reporting and analyzing medical metrics
• Demonstrated ability to build a team and develop a high performing organization (inclusive coaching and mentoring)
Of advantage:
• Knowledge and understanding of BMS Policies and Procedures
• Knowledge of statistical methods
• Solid track record in writing quality scientific publications and representing BMS at international congresses
• Knowledge of Disease Area and local health care system/market dynamics
• Understanding of environmental and industry trends and their impact on the business
• Understanding of product-specific pricing issues and required contribution to pricing and reimbursement dossiers