脈通智造?在全球各地擁有超過900名員工。我們不斷尋找有動力、熱情和才華的人才,與我們攜手共進,共同實現目標。如果您對企業運營的解決方案充滿熱情,我們真誠地邀請您瀏覽我們的空缺職位并加入我們。

中國
浙江嘉興
球囊導管事業部
全職
1、 依據公司及事業部發展戰略,制定技術部工作規劃,技術路線,產品規劃,人才規劃,項目計劃;
2、 技術部運營管理: 產品開發項目,NPI項目,改善項目管理,重大事項決策,達成技術部管理指標;
3、 技術引進和革新,參與并監督產品的立項、研發、實施。主導知識產權策略的制訂、產權保護、引進,相關人才發掘及引進、培養;
4、 運營技術、工藝保障,參與并監督產品轉生產后質量、成本和效率的保證。主導推進制造設備、制造工藝的革新;
5、 團隊建設、人員考核,士氣提升以及事業部總經理安排的其他工作。
1、持續推進工藝研發工作,突破現有球囊/導管制造方法的局限性,保證在質量、成本和效率上擁有絕對競爭力;
2、球囊導管介入8年以上產品研發或工藝經驗,植入/介入產品領域8年以上產品研發或工藝經驗,5年以上技術團隊管理經驗團隊規模不少于5人;
1、博士及以上學歷,高分子材料及相關專業;
2、球囊導管介入5年以上產品研發或工藝經驗,植入/介入產品領域8年以上經驗,5年以上技術團隊管理經驗,團隊規模不少于5人;
3、有特殊貢獻者可放寬;
1、能洞悉行業競品產品優劣勢,未來產品技術方向,具備產品策劃與開發,有項目管理經驗和供應鏈管理經驗;
2、有良好的溝通、協作、學習能力,具備人才梯隊化管理能力、自我驅動能力強,有企業家精神。
中國
上海
業務拓展部
全職
1、積極拜訪現有客戶,挖掘新項目,挖掘客戶潛力,完成銷售額指標;
2、深度理解客戶要求,協調內部資源,滿足客戶需要;
3、開發新客戶,提高未來銷售潛力;
4、與支持部門合作,落實商務合同,技術標準,框架協議等;
5、搜集市場信息及競爭對手信息。
1、新區域新客戶挖掘、增加客戶粘性;
2、關注市場動態,行業變化,從而發現新機遇。
1、碩士及以上學歷,工科類專業背景優先;
2、3年以上To B 直銷經驗,3年以上醫療器械行業經驗。
1、積極主動,有自控力。有良好的客戶服務意識,有介入植入醫療器械背景、了解金屬材料部件產品優先;
2、能適應出差,出差比例大于50% 。
中國
上海或浙江嘉興
高分子材料業務、醫用金屬材料事業部、紡織事業部
全職
1、負責醫療器械材料、零配件相關新技術調研;
2、負責醫療器械材料、零配件前瞻可行性研究;
3、負責醫療器械材料、零配件質量、性能方面的工藝技術提升;
4、負責醫療器械材料、零配件的技術文件和質量文件,包括開發資料、質量標準和專利等。
1、業內前沿技術的鉆研,推動新技術新材料的應用;
2、整合資源,推進項目節奏,快速進行新產品新項目孵化量產。
1、博士及以上學歷,高分子材料、金屬材料、紡織材料及相關專業;
2、3年以上產品研發,植入醫療產品相關工作經驗;
3、有特殊貢獻者可放寬;
1、熟練掌握材料加工專業知識;
2、英語聽說讀寫熟練,具備較好的溝通能力、協調能力以及組織能力。
中國
上海或浙江嘉興
高分子材料業務、醫用金屬材料事業部、紡織事業部
全職
1、對工藝進行過程確認和不斷改進;
2、對產品異常處理,分析不合格原因并采取相應的糾正預防措施;
3、負責相關產品工藝和原材料設計,理解整個產品實現過程中的工藝難點、相關風險及控制措施;
4、根據產品及市場需求,了解競品的主產品構成、并提出產品解決方案。
1、優化產品穩定性,提升產品質量;
2、降本增效,新工藝開發及風險把控。
1、博士及以上學歷,高分子材料、金屬材料、紡織材料及相關專業;
2、2年以上技術類相關工作經驗,2年醫療行業或高分子行業相關工作經驗;
3、有特殊貢獻者可放寬;
1、熟悉材料加工工藝,了解精益生產和六西格瑪,并能提高產品質量,實現產品優化;
2、具備較好的溝通協作能力、擁有獨立分析解決問題能力,并能持續學習,有一定抗壓力。
中國
上海或浙江嘉興
高分子材料業務、醫用金屬材料事業部、紡織事業部
全職
1、質量控制,及時處理產品質量異常,保障產品質量符合性;(NCCAPA材料評價測量系統分析工藝變更工藝變更質量控制風險管理質量追溯);
2、質量改進與支持,配合工藝驗證工作,把關工藝變更風險識別和評價完整性;(變更控制標準分析質量優化檢驗優化);
3、質量體系與監控;
4、識別產品質量隱患和改進機會,并改善實施,保障產品質量風險可控;
5、不斷尋求優化產品質量監控的方法,提升質量監控方法的穩定性和可靠性;
6、上級指派的其他工作任務。
1、根據產品及產線發展,策劃質量管理方案、推動質量改進,提高產品質量;
2、持續推動質量風險預防、控制和改善,提升來料、制程、成品質量,降低客訴。
1、博士及以上學歷,高分子材料、金屬材料、紡織材料及相關專業;
2、5年以上同崗位經驗,有醫療器械行業技術背景者優先;
3、有特殊貢獻者可放寬;
1、了解醫療器械相關法規標準和ISO13485、有新項目質量管理經驗、有FMEA和質量相關統計能力,熟練運用質量工具,熟悉六西格瑪管理;
2、具備問題分析、溝通及協作能力、時間管理及抗壓能力、心智與心理成熟度、創新能力。
United States
Irvine, CA
Full-time (100%)
● Market analysis: Collect and provide feedback on market information based on the company's market strategy, local market characteristics, and industry status.
● Market expansion: Develop sales plans, explore potential markets, identify customer needs, and provide solutions. Optimize sales plans based on market research and analysis to achieve sales targets.
● Customer management: Consolidate and summarize customer information, develop customer visit plans, and maintain customer relationships. Implement the signing of business contracts, confidentiality agreements, technical standards, framework service agreements, etc. Manage order delivery, payment schedules, and confirmations of goods export documents. Contact and follow up on post-sales issues.
● Marketing activities: Plan and participate in various marketing activities, such as relevant medical exhibitions, industry conferences, and key product promotion meetings.
● Cultural differences: Different countries and regions have diverse cultural backgrounds and values, which can result in variations in product positioning, marketing, and sales strategies. Understanding and adapting to the local culture is crucial for successful sales.
● Legal and regulatory issues: Different countries and regions have varying laws and regulations, particularly regarding trade, product standards, and intellectual property. You need to understand and comply with the applicable laws and regulations to ensure compliant operations.
● Bachelor's degree or higher, preferably in Polymer Materials.
● Fluent English; knowledge of Spanish or Portuguese is preferred. Familiarity with the local medical device market environment. 5+ years of business development experience in the medical device or polymer material application field.
● Ability to independently develop customers, negotiate, and communicate internally and externally with multiple parties.
● Proactive, team-oriented, and adaptable to business trips.
United States
Irvine, CA
Full-time (100%)
● Organize and operate the overall quality work in accordance with local laws and regulations. Establish the company's quality management system and ensure its compliance.
● Manage and improve quality effectiveness through regular checks and internal audit programs.
● Lead CAPA and complaint reviews, management reviews, and risk management development with the functional team. Monitor the quality compliance of overseas suppliers.
● Develop, implement, and maintain the quality management system (QMS) for the entire process control. Coordinate external and corporate audits and maintain quality management system certification.
● Verify components and final products during factory transfer to ensure adequate and effective product evaluation.
● Review SOPs to ensure compliance with regulatory requirements. Address related quality issues and assume responsibility for daily product quality release. Maintain an integrated documentation system and guide execution at each manufacturing site. Utilize data analysis skills to identify common risks/issues and provide solutions.
● Establish test methods, carry out method validation and verification, conduct laboratory testing, and ensure effective operation of the laboratory system.
● Arrange manpower for inspecting raw materials, semi-finished products, and finished products to ensure compliance with quality standards.
● Provide training, communication, and advice.
● Regulations and Compliance: The medical device industry is subject to strict regulations and compliance requirements. As a quality manager, you need to ensure that products comply with these regulations and standards and that company operations align with relevant requirements.
● Quality Control: Quality control is crucial in the medical device industry as product quality directly affects patient health and safety. You need to ensure that the company's quality management system operates effectively, including the ability to detect, assess, and resolve quality issues.
● Risk Management: Medical device manufacturing involves certain risks, including product failures, safety issues, and legal liabilities. As a quality manager, you need to effectively manage and mitigate these risks to ensure the company's reputation and interests are not compromised.
● Bachelor's degree or above in science and engineering. Advanced degree preferred.
● 7+ years of experience in quality-related roles, preferably in a manufacturing environment.
● Familiarity with ISO 13485 quality system and regulatory standards such as FDA QSR 820 and Part 211.
● Experience in constructing quality system documents and conducting compliance audits.
● Strong presentation skills and experience as a trainer.
● Excellent interpersonal skills with a proven ability to effectively interact with multiple organizational units.
● Proficient in the application of quality tools such as FMEA, statistical analysis, process validation, etc.


