Sr Supplier Development Engineer
百特(中国)投资有限公司
- 公司规模:500-1000人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2022-06-27
- 工作地点:广州
- 工作经验:3-4年经验
- 学历要求:本科
- 语言要求:英语熟练
- 职位月薪:1.5-2.5万·13薪
- 职位类别:供应商管理
职位描述
Position Overview
The Senior Supplier Development Engineer is responsible to execute supplier development processes, tools and strategies, to continuously improve suppliers performance to mitigate risks in terms of Quality, Delivery, Capacity, Cost & Sustainability.
Reporting to the Director of Supplier Development Director, this highly visible role will also focus on will be responsible for engaging in conversations with suppliers to ensure process metrics are defined, controls are in place for critical features and gaps are identified in the supplier quality management. They will drive development action plans and projects to ensure supplier’s products will be consistent in quality to enable flawless execution and delivery of product strategic. If you’re ready to make an impact within a fast paced, dynamic global environment this could be the perfect role for you!
Additional Responsibilities:
Directly support supplier quality during new product development (NPI)
Work with suppliers during new product development to implement process controls and develop quality assurance plans for purchased parts
Conduct direct supplier assessments, including supplier audits and quality control reviews
Develop and implement supplier risk mitigation strategies
Execute contracts and quality plans with suppliers to ensure compliance with quality requirements
Develop, implement and monitor early supplier quality development initiatives including performance management, supplier certification, process improvements, cost reduction, supplier forums and Six Sigma/Lean integration
Lead qualification efforts for new supplier parts, including development of capability studies, control plans, first article inspections, and PFMEAs, and review and approval of supplier design changes and change requests
Work with engineering to identify receiving inspection requirements for purchased components and finished goods. Provide technical quality support for incoming inspection
Work with supplier engineering and quality management teams to efficiently resolve reported issues and implement actions to preclude reoccurrence of identified issues.
Measure and communicate supplier performance against key quality metrics and project milestones.
Drive continuous improvement in supplier performance through the use of tools such as DOE, Six Sigma, DMAIC, FMEA, SPC, 8D Root Cause Analysis and Lean including increasing supplier knowledge and implementation of these quality tools and techniques
Assist in the investigation of complaints and returns related to purchased products caused by the supplier
Assist with internal CAPA (Corrective Action Preventive Action) activities that are dependent on SCAR.
Qualifications:
Bachelor’s degree in Science- engineering- Completed engineering studies or comparable technical qualification Knowledge of electrical engineering / electronics as well as practical experience in measurement, testing, inspection and analysis technology required
Several years of experience in supplier evaluation and auditing as well as experience in manufacturing, quality assurance and/or design
Knowledge of US medical device regulations as well as exposure to standard quality system requirements (ISO 9001, ISO 13485, Medical Device Directives)
Experience in supplier support or supplier development required
Excellent analytical and problem solving skills as well as data analysis and presentation skills
Ability to work independently while motivating and driving team initiatives
Excellent time management and ability to multi-task and methodically manage project milestones
Fluent in business English and experience and MS Office, knowledge of Minitab, Tableau and JD Edwards is a plus
ASQ certification (Certified Quality Engineer, Certified Quality Auditor, Certified Biomedical Auditor) are preferable
Ability to travel up to 35%
Ability to communicate in English fluently is a MUST
The Senior Supplier Development Engineer is responsible to execute supplier development processes, tools and strategies, to continuously improve suppliers performance to mitigate risks in terms of Quality, Delivery, Capacity, Cost & Sustainability.
Reporting to the Director of Supplier Development Director, this highly visible role will also focus on will be responsible for engaging in conversations with suppliers to ensure process metrics are defined, controls are in place for critical features and gaps are identified in the supplier quality management. They will drive development action plans and projects to ensure supplier’s products will be consistent in quality to enable flawless execution and delivery of product strategic. If you’re ready to make an impact within a fast paced, dynamic global environment this could be the perfect role for you!
Additional Responsibilities:
Directly support supplier quality during new product development (NPI)
Work with suppliers during new product development to implement process controls and develop quality assurance plans for purchased parts
Conduct direct supplier assessments, including supplier audits and quality control reviews
Develop and implement supplier risk mitigation strategies
Execute contracts and quality plans with suppliers to ensure compliance with quality requirements
Develop, implement and monitor early supplier quality development initiatives including performance management, supplier certification, process improvements, cost reduction, supplier forums and Six Sigma/Lean integration
Lead qualification efforts for new supplier parts, including development of capability studies, control plans, first article inspections, and PFMEAs, and review and approval of supplier design changes and change requests
Work with engineering to identify receiving inspection requirements for purchased components and finished goods. Provide technical quality support for incoming inspection
Work with supplier engineering and quality management teams to efficiently resolve reported issues and implement actions to preclude reoccurrence of identified issues.
Measure and communicate supplier performance against key quality metrics and project milestones.
Drive continuous improvement in supplier performance through the use of tools such as DOE, Six Sigma, DMAIC, FMEA, SPC, 8D Root Cause Analysis and Lean including increasing supplier knowledge and implementation of these quality tools and techniques
Assist in the investigation of complaints and returns related to purchased products caused by the supplier
Assist with internal CAPA (Corrective Action Preventive Action) activities that are dependent on SCAR.
Qualifications:
Bachelor’s degree in Science- engineering- Completed engineering studies or comparable technical qualification Knowledge of electrical engineering / electronics as well as practical experience in measurement, testing, inspection and analysis technology required
Several years of experience in supplier evaluation and auditing as well as experience in manufacturing, quality assurance and/or design
Knowledge of US medical device regulations as well as exposure to standard quality system requirements (ISO 9001, ISO 13485, Medical Device Directives)
Experience in supplier support or supplier development required
Excellent analytical and problem solving skills as well as data analysis and presentation skills
Ability to work independently while motivating and driving team initiatives
Excellent time management and ability to multi-task and methodically manage project milestones
Fluent in business English and experience and MS Office, knowledge of Minitab, Tableau and JD Edwards is a plus
ASQ certification (Certified Quality Engineer, Certified Quality Auditor, Certified Biomedical Auditor) are preferable
Ability to travel up to 35%
Ability to communicate in English fluently is a MUST
公司介绍
百特国际有限公司提供肾科与医院关键产品的广泛组合,包括居家透析、急重症透析和中心透析产品;无菌静脉输液;输注系统与设备;肠外营养;生物外科产品与麻醉;以及药房自动化、软件和服务。公司凭借全球布局,以及其产品与服务的必需性,在提升新兴与发达国家市场医疗可及性方面发挥至关重要的作用。百特在全球的五万名员工,秉承公司在医疗创新领域的深厚积淀,持续推动未来的医疗创新,更好地满足患者的医疗需求。
Baxter International Inc. provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; biosurgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s 50,000 employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.
Baxter International Inc. provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; biosurgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s 50,000 employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.
联系方式
- Email:TTA@baxter.com
- 公司地址:杭州