【Job Responsibilitie】
1. Plan, Coordinate, and Monitor Feasibility R&D Projects:
- Support the CTO in planning and coordinating cross-disciplinary R&D feasibility studies and projects.
- Define technical requirements, deliverables, and timelines in collaboration with stakeholders and experts.
- Communicate effectively with R&D, Operations, Marketing, Regulatory, Clinical teams, suppliers, and external partners.
- Manage NDAs and contracts with third-party collaborators when needed.
- Provide regular progress reports, meeting minutes, and summaries.
2. Initiate Formal Project Kick-offs
- Launch formal projects (product life cycle management) upon successful completion of feasibility phases. Create final feasibility study report, assist with responsibility transfer to cite managers.
- Coordinate and transfer information to ensure smooth and successful implementation at project sites.
- Facilitate communication among stakeholders and provide initial support for new projects.
3. Support Process Flow with Technical Information Collection
- Gather and analyze technical data and product specifics from marketing materials, patent applications, scientific articles, and key opinion leaders.
- Develop rationales and justifications for project decisions.
- Apply for government-sponsored programs and navigate policies to support innovative developments.
4. Provide Technical Assistance to the CTO
- Compose concise technical summaries and reports.
- Review competitor technologies, products, and analyze key players’ patent portfolios. Closely communicate with Marketing colleagues.
- Offer comprehensive daily technical support to aid strategic decision-making.
【Qualification for Employment】
1.Educational degree/major/age
- Degree: Minimum Master’s Degree (MSc) in a technical discipline such as Mechanical, Electrical, Optical, Chemical Engineering, or related fields.
- Age: 25–45 years.
2.Relevant work experience
- Industries: Experience in the medical device, pharmaceutical, or medical equipment sectors.
- Project skills: Experience with project coordination and monitoring.
- Preferred: Background in the ophthalmic industry is highly advantageous!
3.Employability skills (relevant vocational competencies matched with job requirements, ranked by importance)
- Industry Experience: Over 5 years in the medical device or pharmaceutical industries.
- Adaptability & Creativity: Demonstrated ability to learn quickly and innovate. Initiative and open-minded!
- Communication: Skilled in building and maintaining effective communication channels among diverse stakeholder groups.
- Project Management: Proficient in project coordination and management, with knowledge of relevant tools and software.
- Technical Proficiency: Experience working with technical and scientific information, including technical study reports, patents and research articles. Ability to summarize information and identify key details.
- Regulatory and QA Knowledge: Understanding the principles of ISO 13485, or 21 CFR, and other Quality Management System (QMS) requirements specific for medical device industry, particularly Design Control and Change Control procedures.
- Additional Skills: Competence in data analysis, statistics, programming, optics, materials, or related areas is a plus.
4.Additional requirements
- Perfect English, written and spoken, ability to comunicate clearly on technical subjects and use commonly accepted terminology.
- Positive attitude to work and colleagues.
【崗位職責】
1. 規劃、協調和管控可行性研發項目:
- 在CTO的協助下規劃和協調跨學科的研發可行性研究和項目。
- 與利益相關者和專家合作定義技術要求、交付成果和時間表。
- 與研發、運營、市場、監管、臨床團隊、供應商和外部合作伙伴有效溝通。
- 在需要時管理與第三方合作者的保密協議和合同。
- 提供定期進度報告、會議記錄和摘要。
2. 啟動正式項目啟動
- 在可行性階段成功完成后,啟動正式項目(產品生命周期管理)。創建最終的可行性研究報告,協助責任轉移給項目經理。
- 協調和轉移信息以確保項目現場的順利和成功實施。
- 促進利益相關者之間的溝通,并為新項目提供初步支持。
3. 通過技術信息收集支持流程
- 收集和分析來自市場資料、專利申請、科學文章和關鍵意見領袖的技術數據和產品細節。
- 為項目決策制定理由和依據。
- 申請政府資助項目并導航政策以支持創新發展。
4. 為CTO提供技術支持
- 撰寫簡潔的技術摘要和報告。
- 審查競爭對手的技術、產品,并分析關鍵玩家的專利組合。與市場同事密切溝通。
- 提供全面的日常技術支持以協助戰略決策。
【任職資格】
1. 教育程度/專業/年齡
- 學位:機械、電氣、光學、化學工程或相關專業的碩士及以上學位。
- 年齡:25至45歲。
2. 相關工作經驗
- 在醫療器械、制藥或醫療設備領域有經驗。
- 有項目協調和管控經驗。
- 具備眼科行業背景優先考慮
3. 技能(與工作要求相匹配的相關職業技能,按重要性排序)
- 行業經驗:在醫療器械或制藥行業超過5年的工作經驗。
- 適應性與創造力:展現出快速學習和創新的能力。積極主動和思維開放!
- 溝通:擅長建立和維護有效的溝通渠道。
- 項目管理:熟練進行項目協調和管理,了解相關工具和軟件。
- 技術熟練度:有處理技術性和科學性信息的經驗,包括技術研究報告、專利和研究文章。能夠總結信息并識別關鍵細節。
- 法規和質量保證知識:理解ISO13485或21CFR以及其他針對醫療器械行業的質量管理系統(QMS)要求,特別是設計控制和變更控制程序。
- 其他技能:數據分析、統計、編程、光學、材料或相關領域的技能是加分項。
4. 其他要求
- 英語能熟練運用于書面或口語,并且能夠在專業技術上清晰溝通并使用術語。
- 協同意識佳、工作態度積極。