應屆畢業(yè)生
本科
2026-02-13 00:00:19
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職位描述
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在羅氏，我們鼓勵每位同事展現(xiàn)真實的自己；我們欣賞獨特且出眾的品質。羅氏的文化鼓勵積極的表達、開放的對話和真誠的連結，在這里，你將因為做自己而被重視、接納和尊重，并得到個人的提升和職業(yè)的發(fā)展。所有的這一切，都是為了更好地預防、阻止和治愈疾病，并確保醫(yī)療資源的可及性和可持續(xù)性。歡迎加入羅氏，一個重視每種聲音的地方。
職位
● Execute eCTD submission activities (including but not limited to planning, coordination, compilation, publishing, and submissions of regulatory applications) in line with submission/content strategy and in compliance with internal processes and external regulations, to ensure high quality and timely submission with Health Authority.
● Support and contribute to the full adoption of eCTD submissions, to ensure fulfillment of evolving agency requirements and corporate standards, including but not limited to system testing and integration, tool enhancement, pilot submissions delivery.
● Contribute to eCTD capability building by setting up eCTD submission readiness in terms of infrastructure, process, etc. and exploring optimal working models in terms of collaborations with multiple business partners (including but not limited to vendors, Global teams, stakeholders).
● Provide eCTD training and support knowledge management to relevant colleagues, teams and stakeholders for necessary understanding of eCTD requirements and to ensure smooth collaborations from a cross-functional perspective for submission excellence.
● Stay updated on the latest regulatory regulations, guidelines and changes; and interpret and foresee the impact on corporate practice and process with proactive mitigation and applicable solutions.
● Contribute to vendor oversight for excellent delivery with optimized model and process.
● Support the development and implementation of the strategic plans for eCTD submissions in alignment with the organization’s portfolio priorities.
● Support the group leader on exploring new ways of working to achieve a high-performance organization.
eCTD Expertise
● Solid knowledge of regulatory agency requirements for electronic submissions format and delivery including profuse knowledge of eCTD specifications and validation requirements.
● Practical hands-on experiences in executing eCTD applications involving the assembly, formatting, publishing and submissions of regulatory dossiers with HAs.
● Expertise in eCTD publishing process and tools, submission software, documents management systems; proficiency with relevant IT tools, especially MS Office programs (Word, Excel) and Adobe Acrobat; experience of working with RIM/Veeva Vault systems is a plus.
● Motivated self-starter with the sensitivity to detect potential impact raised by regulation change and the ability to identify opportunities for process improvement.
Operational Excellence Version date: Dec 2025 Page 1 of 2
● Ability to effectively plan, execute, and monitor projects from initiation to completion with minimum guide.
● Capability to collaborate with diverse stakeholders to ensure alignment and support, by building and maintaining trustful and strong relationships, proactively managing stakeholder expectations, with strong interpersonal and communication skills to influence and negotiate effectively.
● Ability to work effectively within a team and across departments to achieve common goals, by developing and cultivating robust relationships with colleagues at all levels of the organization, fostering a collaborative work environment inclusively, supporting team members by sharing knowledge and providing technical-shooting assistance/insights inputs, etc. ● A strong commitment to continuous learning and self-improvement, with a demonstrated ability to quickly manage usage of new systems and tools, acquire new knowledge and skills, adapt to changing environments, stay updated with industry trends and best practices; and the ability to learn from feedback and incorporate it into personal and professional growth.
Education/Qualifications ● B.S. or above in Pharmacy, Medical, Biology or related field
Relevant working experience:
職位
● Execute eCTD submission activities (including but not limited to planning, coordination, compilation, publishing, and submissions of regulatory applications) in line with submission/content strategy and in compliance with internal processes and external regulations, to ensure high quality and timely submission with Health Authority.
● Support and contribute to the full adoption of eCTD submissions, to ensure fulfillment of evolving agency requirements and corporate standards, including but not limited to system testing and integration, tool enhancement, pilot submissions delivery.
● Contribute to eCTD capability building by setting up eCTD submission readiness in terms of infrastructure, process, etc. and exploring optimal working models in terms of collaborations with multiple business partners (including but not limited to vendors, Global teams, stakeholders).
● Provide eCTD training and support knowledge management to relevant colleagues, teams and stakeholders for necessary understanding of eCTD requirements and to ensure smooth collaborations from a cross-functional perspective for submission excellence.
● Stay updated on the latest regulatory regulations, guidelines and changes; and interpret and foresee the impact on corporate practice and process with proactive mitigation and applicable solutions.
● Contribute to vendor oversight for excellent delivery with optimized model and process.
● Support the development and implementation of the strategic plans for eCTD submissions in alignment with the organization’s portfolio priorities.
● Support the group leader on exploring new ways of working to achieve a high-performance organization.
eCTD Expertise
● Solid knowledge of regulatory agency requirements for electronic submissions format and delivery including profuse knowledge of eCTD specifications and validation requirements.
● Practical hands-on experiences in executing eCTD applications involving the assembly, formatting, publishing and submissions of regulatory dossiers with HAs.
● Expertise in eCTD publishing process and tools, submission software, documents management systems; proficiency with relevant IT tools, especially MS Office programs (Word, Excel) and Adobe Acrobat; experience of working with RIM/Veeva Vault systems is a plus.
● Motivated self-starter with the sensitivity to detect potential impact raised by regulation change and the ability to identify opportunities for process improvement.
Operational Excellence Version date: Dec 2025 Page 1 of 2
● Ability to effectively plan, execute, and monitor projects from initiation to completion with minimum guide.
● Capability to collaborate with diverse stakeholders to ensure alignment and support, by building and maintaining trustful and strong relationships, proactively managing stakeholder expectations, with strong interpersonal and communication skills to influence and negotiate effectively.
● Ability to work effectively within a team and across departments to achieve common goals, by developing and cultivating robust relationships with colleagues at all levels of the organization, fostering a collaborative work environment inclusively, supporting team members by sharing knowledge and providing technical-shooting assistance/insights inputs, etc. ● A strong commitment to continuous learning and self-improvement, with a demonstrated ability to quickly manage usage of new systems and tools, acquire new knowledge and skills, adapt to changing environments, stay updated with industry trends and best practices; and the ability to learn from feedback and incorporate it into personal and professional growth.
Education/Qualifications ● B.S. or above in Pharmacy, Medical, Biology or related field
Relevant working experience:
注：聯(lián)系我時，請說是在江蘇人才網(wǎng)上看到的。
工作地點
地址：濮陽華龍區(qū)正大中心
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詳細位置，可以參考上方地址信息
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職位發(fā)布者
唐靜如HR
上海羅氏制藥有限公司
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制藥·生物工程
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1000人以上
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中外合資（合資·合作）
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浦東新區(qū)龍東大道1100號
