崗位職責(zé)是什么
工藝項(xiàng)目崗位，是企業(yè)中負(fù)責(zé)規(guī)劃、實(shí)施和優(yōu)化生產(chǎn)工藝流程的關(guān)鍵角色。這個職位的核心任務(wù)是確保生產(chǎn)過程的高效、安全和質(zhì)量，以滿足公司的業(yè)務(wù)目標(biāo)和客戶需求。
崗位職責(zé)要求
1. 精通各類制造工藝，包括但不限于機(jī)械、化學(xué)、電子等領(lǐng)域，具備扎實(shí)的理論知識和實(shí)踐經(jīng)驗(yàn)。
2. 具備優(yōu)秀的項(xiàng)目管理能力，能有效地協(xié)調(diào)資源，控制項(xiàng)目進(jìn)度，確保按時交付。
3. 熟悉質(zhì)量管理體系，如iso 9001，能夠制定和維護(hù)工藝流程標(biāo)準(zhǔn)。
4. 具備良好的分析能力和問題解決技巧，能夠在遇到生產(chǎn)問題時迅速提出解決方案。
5. 能夠與跨部門團(tuán)隊(duì)有效溝通，包括工程、生產(chǎn)、采購和質(zhì)量保證等部門。
6. 持續(xù)關(guān)注行業(yè)發(fā)展趨勢，引進(jìn)新技術(shù)，提升工藝效率和產(chǎn)品質(zhì)量。
崗位職責(zé)描述
工藝項(xiàng)目崗位的工作日常涉及深入理解產(chǎn)品設(shè)計(jì)，制定詳細(xì)的生產(chǎn)工藝流程，并監(jiān)督其執(zhí)行。此崗位需要不斷優(yōu)化現(xiàn)有的工藝，消除生產(chǎn)瓶頸，提高生產(chǎn)效率。此外，還需要處理與供應(yīng)商、內(nèi)部團(tuán)隊(duì)及客戶的關(guān)系，確保工藝流程的合規(guī)性和滿意度。在面對技術(shù)挑戰(zhàn)時，工藝項(xiàng)目經(jīng)理需要展現(xiàn)出創(chuàng)新思維，尋找改進(jìn)工藝的新方法，以推動企業(yè)技術(shù)進(jìn)步。
有哪些內(nèi)容
1. 工藝規(guī)劃：分析產(chǎn)品設(shè)計(jì)，制定可行的生產(chǎn)工藝方案，預(yù)測可能的風(fēng)險(xiǎn)和挑戰(zhàn)。
2. 項(xiàng)目實(shí)施：組織和協(xié)調(diào)資源，確保工藝項(xiàng)目的順利進(jìn)行，包括設(shè)備采購、人員培訓(xùn)等。
3. 過程控制：監(jiān)控生產(chǎn)過程，確保符合工藝標(biāo)準(zhǔn)，及時調(diào)整工藝參數(shù)以保證產(chǎn)品質(zhì)量。
4. 質(zhì)量管理：參與質(zhì)量審核，制定和執(zhí)行質(zhì)量控制措施，防止質(zhì)量問題的發(fā)生。
5. 技術(shù)改進(jìn)：研究新工藝，引入先進(jìn)設(shè)備和技術(shù)，提升生產(chǎn)效率和產(chǎn)品質(zhì)量。
6. 培訓(xùn)指導(dǎo)：為生產(chǎn)團(tuán)隊(duì)提供工藝培訓(xùn)，確保員工理解和掌握生產(chǎn)工藝。
7. 內(nèi)外部溝通：與供應(yīng)商協(xié)商材料和設(shè)備供應(yīng)，與內(nèi)部團(tuán)隊(duì)協(xié)調(diào)工作，向客戶提供工藝技術(shù)支持。
8. 文檔編制：編寫和更新工藝流程文檔，確保工藝知識的有效傳遞和標(biāo)準(zhǔn)化。
工藝項(xiàng)目崗位是一個集技術(shù)、管理和創(chuàng)新于一體的職位，需要從業(yè)者具備全面的專業(yè)技能和卓越的領(lǐng)導(dǎo)力，以驅(qū)動企業(yè)的工藝改進(jìn)和生產(chǎn)效率提升。
工藝項(xiàng)目崗位職責(zé)范文
第1篇 項(xiàng)目建設(shè)部熔鑄工藝技術(shù)員崗位職責(zé)
1. 協(xié)助領(lǐng)導(dǎo)做好各項(xiàng)目組的規(guī)劃建設(shè)
2. 協(xié)調(diào)項(xiàng)目建設(shè)過程中與設(shè)計(jì)院往來問題落實(shí)
3. 協(xié)助領(lǐng)導(dǎo)做好項(xiàng)目建設(shè)過程中文件管理工作
4. 協(xié)助領(lǐng)導(dǎo)完成項(xiàng)目進(jìn)度考核工作
5. 協(xié)助領(lǐng)導(dǎo)做好項(xiàng)目建設(shè)過程中文件管理工作
6. 按時準(zhǔn)確的完成領(lǐng)導(dǎo)交辦的其他工作
第2篇 項(xiàng)目工藝工程師崗位職責(zé)范本
1.負(fù)責(zé)指派在p1項(xiàng)目前刮水、后刮水系統(tǒng)的工藝開發(fā)工作。
2.是前刮水、后刮水系統(tǒng)項(xiàng)目開發(fā)過程中的主要技術(shù)支持者。
3.確保所有的p1項(xiàng)目前刮水、后刮水系統(tǒng)的工藝開發(fā)。
第3篇 項(xiàng)目制造工藝工程師崗位職責(zé)內(nèi)容
1.消化產(chǎn)品圖紙、數(shù)據(jù)及實(shí)樣,編制產(chǎn)品報(bào)價bom、工藝流程、設(shè)備模具清單等資料,支持新業(yè)務(wù)可行性評審和報(bào)價。
2.參加新產(chǎn)品開發(fā)項(xiàng)目組,并負(fù)責(zé)新項(xiàng)目開發(fā)過程中的制造工程開發(fā)工作。
3.負(fù)責(zé)編制批產(chǎn)前的相關(guān)技術(shù)文件。
4.協(xié)助制造部門進(jìn)行持續(xù)改進(jìn)工作。
第4篇 項(xiàng)目制造工藝工程師崗位職責(zé)
項(xiàng)目制造工藝工程師 延鋒彼歐 延鋒彼歐汽車外飾系統(tǒng)有限公司,延鋒彼歐,延鋒彼歐汽車外飾系統(tǒng),延鋒彼歐 職責(zé)描述:
1.主導(dǎo)新業(yè)務(wù)項(xiàng)目前期工程報(bào)價,消化產(chǎn)品圖紙、數(shù)據(jù)及實(shí)樣,編制產(chǎn)品報(bào)價bom、工藝流程、工裝設(shè)備模具清單等資料;
2.承擔(dān)項(xiàng)目前期產(chǎn)品結(jié)構(gòu)設(shè)計(jì)的制造工藝可行性分析,輸出評審及可行性報(bào)告,并根據(jù)評審結(jié)果跟蹤產(chǎn)品數(shù)據(jù)的優(yōu)化改進(jìn);
3.組織原材料、油漆、模/檢具、工裝設(shè)備等各階段技術(shù)可行性評審及認(rèn)可,簽訂技術(shù)協(xié)議,并跟蹤設(shè)備、工裝模具的制造過程,會同有相關(guān)部門參與完成模/檢具、工裝設(shè)備等驗(yàn)收和安裝調(diào)試;
4.組織新產(chǎn)品試制、工藝調(diào)試和工藝驗(yàn)證、各階段工程評審,實(shí)施和跟蹤工程更改,按客戶的認(rèn)可流程進(jìn)行產(chǎn)品認(rèn)可,支持內(nèi)部工廠投產(chǎn)準(zhǔn)備,并主導(dǎo)編制批產(chǎn)前的相關(guān)技術(shù)文件,qad代碼申請、新產(chǎn)品試制時的物料申請等;
5.經(jīng)驗(yàn)教訓(xùn)總結(jié)和專項(xiàng)工藝技術(shù)總結(jié)分享;
6.支持新項(xiàng)目sop后6個月內(nèi)的工程問題解決;
7.完成領(lǐng)導(dǎo)安排的其他工作。
任職要求:
學(xué)歷及工作經(jīng)驗(yàn): 本科 2年及以上相關(guān)工作經(jīng)驗(yàn)
專業(yè)背景: 機(jī)械, 模具,高分子,車輛工程或其他相關(guān)專業(yè)
體系要求 :
質(zhì)量: ts16949系列標(biāo)準(zhǔn)(含顧客特殊要求)
環(huán)保: iso14001體系標(biāo)準(zhǔn)和相關(guān)法律法規(guī)
安全: ohsas18001體系標(biāo)準(zhǔn)和相關(guān)法律法規(guī)、職業(yè)病防治法
第5篇 項(xiàng)目工藝崗位職責(zé)任職要求
項(xiàng)目工藝崗位職責(zé)
項(xiàng)目工藝 has a detailed understanding and e_pertise in the field of processes hereafter to support current p2 & p1 industrial & design teams
- act as a member of the development team， participate to the design reviews， guide design teams to reach design to costs， design for manufacturing & optimized investments
- work in collaboration with geeds & pel power-module métier hw & mk teams
- is responsible to setup the process (definition of process equipments & toolings， process parameters) for mock-ups & prototypes
- is responsible to train the prototype apu member and transfer the operator level knowledge
- work on mass-production implementation scenario & define options， key constraints， industrial planning， investments
- contribute to product & process fmea for the processes he/she is in charge
- identify & perform does to determine key process parameters & optimize process (cycle time， scrap level， cape_， labour cost)
- develop process control parameters to ensure compliance with product specifications
- support transition of newly developed processes into series production， providing process / equipment specification， work instruction， training to apu
- develop an industrial cross-project competence for all power-modules under development
- support root-cause analysis & corrective actions for problem solving & continuous improvement
- perform survey of e_isting equipment in the market in a continuous improvement & cost reduction mindset to optimize investments， material & labour costs
-work with the instrumentation of analysis lab whenever necessary
has a detailed understanding and e_pertise in the field of processes hereafter to support current p2 & p1 industrial & design teams
- act as a member of the development team， participate to the design reviews， guide design teams to reach design to costs， design for manufacturing & optimized investments
- work in collaboration with geeds & pel power-module métier hw & mk teams
- is responsible to setup the process (definition of process equipments & toolings， process parameters) for mock-ups & prototypes
- is responsible to train the prototype apu member and transfer the operator level knowledge
- work on mass-production implementation scenario & define options， key constraints， industrial planning， investments
- contribute to product & process fmea for the processes he/she is in charge
- identify & perform does to determine key process parameters & optimize process (cycle time， scrap level， cape_， labour cost)
- develop process control parameters to ensure compliance with product specifications
- support transition of newly developed processes into series production， providing process / equipment specification， work instruction， training to apu
- develop an industrial cross-project competence for all power-modules under development
- support root-cause analysis & corrective actions for problem solving & continuous improvement
- perform survey of e_isting equipment in the market in a continuous improvement & cost reduction mindset to optimize investments， material & labour costs
-work with the instrumentation of analysis lab whenever necessary
項(xiàng)目工藝崗位
第6篇 工藝開發(fā)項(xiàng)目崗位職責(zé)
抗體工藝開發(fā)項(xiàng)目經(jīng)理 senior manager/associate director/director, cmc project lead
job description
position summary
this is an e_citing opportunity for motivated individual to enrich and broaden his/her biopharmaceutical development e_perience for both career advancement, and at the same time, making meaningful impact to patient lives in one of the highly regarded and fast growing biotech companies in china.
this cmc project lead and manager, working with the cmc team members, is responsible for product cmc strategy, planning and e_ecution by leading and managing a cmc team consisting of technical representatives. he/she will support two or more biologics projects in all cmc aspects of product development from clinical phase i to commercialization. the cmc project lead will focus on the cmc strategic and operational aspects of the program while also supporting the team in making comple_ cross-functional decisions (e.g., scenario planning, risk assessment, setting strategic priorities). this role will report to the vp, cmc operations.
responsibilities
the primary responsibility will be leading and managing project cmc team, ensuring that project priorities and plans are developed and e_ecuted in accordance with corporate goals.
? identification, planning, and e_ecution of key program cmc initiatives and milestones to support corporate goals.
? lead the project cmc team in making comple_ cross-functional recommendations / decisions
? lead and manage team meetings and agenda topics, facilitate discussions, propose/recommend key decisions, and follow up with action items.
? ensure alignment of objectives, plans, and activities across various cmc functions (e.g., r&d, process development, analytical chemistry, qc, qa, manufacturing, regulatory affairs, supply chain, etc.).
? familiar with operational aspects of the program and produce documents and visual tools to facilitate project tracking and progress (e.g., decision and action logs, planning trackers, timelines, etc.).
? develop and maintain strong, collaborative relationships with key stakeholders
? ensure that timely and consistent communications regarding program strategy, status and decisions are made within the team and to other stakeholders, including senior management.
qualifications
? education: a bachelor of science in scientific fields (e.g. biology, chemistry, engineering, or pharmacy) required. advanced degree (masters or phd in a scientific discipline) is preferred but not required. professional training/e_perience in project management is a plus.
? 8+ years’ e_perience in a biotech or pharmaceutical organization in drug development with e_pertise/knowledge in such functions as process development, manufacturing and engineering, quality, analytical chemistry, formulation, supply chain, regulatory affairs
self-motivated, and eager to learn; strong ownership, and ability to follow through with direction/tasks; proactive and positive when facing challenges
? comfortable working in a team environment, and can motivate and help others to achieve cmc goals with team efforts
? high degree of professionalism, respectful to others and ability to work in fast-paced and dynamic environment
? working knowledge of overall drug/biologics development process and familiar with various functional areas and their roles within a biotech / pharmaceutical company.
? prior e_perience in supporting pre-clinical and/or clinical-stage drug development programs, preferably across different phases (e.g. phases i–iii).
? some knowledge of cgmp is desirable
?e_cellent collaboration, oral and written communications, influence skills and sound judgment
? ability to communicate to both broader organization and the senior management
? ability to multi-task and shift priorities quickly while working under tight deadlines; ability to work under uncertainty
? attention to detail, highly organizational, and willingness to learn quickly
? good skills in common word processing tools (such as words, powerpoint, e_cel, and ms project)
? title will commensurate with individual’s e_perience and qualifications
senior manager/associate director/director, cmc project lead
job description
position summary
this is an e_citing opportunity for motivated individual to enrich and broaden his/her biopharmaceutical development e_perience for both career advancement, and at the same time, making meaningful impact to patient lives in one of the highly regarded and fast growing biotech companies in china.
this cmc project lead and manager, working with the cmc team members, is responsible for product cmc strategy, planning and e_ecution by leading and managing a cmc team consisting of technical representatives. he/she will support two or more biologics projects in all cmc aspects of product development from clinical phase i to commercialization. the cmc project lead will focus on the cmc strategic and operational aspects of the program while also supporting the team in making comple_ cross-functional decisions (e.g., scenario planning, risk assessment, setting strategic priorities). this role will report to the vp, cmc operations.
responsibilities
the primary responsibility will be leading and managing project cmc team, ensuring that project priorities and plans are developed and e_ecuted in accordance with corporate goals.
? identification, planning, and e_ecution of key program cmc initiatives and milestones to support corporate goals.
? lead the project cmc team in making comple_ cross-functional recommendations / decisions
? lead and manage team meetings and agenda topics, facilitate discussions, propose/recommend key decisions, and follow up with action items.
? ensure alignment of objectives, plans, and activities across various cmc functions (e.g., r&d, process development, analytical chemistry, qc, qa, manufacturing, regulatory affairs, supply chain, etc.).
? familiar with operational aspects of the program and produce documents and visual tools to facilitate project tracking and progress (e.g., decision and action logs, planning trackers, timelines, etc.).
? develop and maintain strong, collaborative relationships with key stakeholders
? ensure that timely and consistent communications regarding program strategy, status and decisions are made within the team and to other stakeholders, including senior management.
qualifications
? education: a bachelor of science in scientific fields (e.g. biology, chemistry, engineering, or pharmacy) required. advanced degree (masters or phd in a scientific discipline) is preferred but not required. professional training/e_perience in project management is a plus.
? 8+ years’ e_perience in a biotech or pharmaceutical organization in drug development with e_pertise/knowledge in such functions as process development, manufacturing and engineering, quality, analytical chemistry, formulation, supply chain, regulatory affairs
self-motivated, and eager to learn; strong ownership, and ability to follow through with direction/tasks; proactive and positive when facing challenges
? comfortable working in a team environment, and can motivate and help others to achieve cmc goals with team efforts
? high degree of professionalism, respectful to others and ability to work in fast-paced and dynamic environment
? working knowledge of overall drug/biologics development process and familiar with various functional areas and their roles within a biotech / pharmaceutical company.
? prior e_perience in supporting pre-clinical and/or clinical-stage drug development programs, preferably across different phases (e.g. phases i–iii).
? some knowledge of cgmp is desirable
?e_cellent collaboration, oral and written communications, influence skills and sound judgment
? ability to communicate to both broader organization and the senior management
? ability to multi-task and shift priorities quickly while working under tight deadlines; ability to work under uncertainty
? attention to detail, highly organizational, and willingness to learn quickly
? good skills in common word processing tools (such as words, powerpoint, e_cel, and ms project)
? title will commensurate with individual’s e_perience and qualifications
第7篇 化工工藝項(xiàng)目崗位職責(zé)
化工工藝項(xiàng)目經(jīng)理 靈匯 靈匯技術(shù)股份有限公司,靈匯,靈匯股份,靈匯 大學(xué)本科,化工,制藥專業(yè)畢業(yè),具有良好的溝通、協(xié)調(diào)能力,熟練掌握cad繪圖技術(shù),有醫(yī)藥,化工工藝設(shè)計(jì)經(jīng)歷。如口服固體制劑車間、口服液車間、小容量注射劑車間、大容量注射劑車間、凍干粉針車間、原料藥車間、醫(yī)療器械等車間的工藝設(shè)計(jì)。
第8篇 項(xiàng)目工藝工程師崗位職責(zé)任職要求
項(xiàng)目工藝工程師崗位職責(zé)
項(xiàng)目工藝工程師 作為項(xiàng)目團(tuán)隊(duì)核心成員和工藝開發(fā)團(tuán)隊(duì)主管，負(fù)責(zé)項(xiàng)目所有制造方面技術(shù)工作，從報(bào)價階段開始直到量產(chǎn)后相關(guān)工作，支持生產(chǎn)現(xiàn)場，解決現(xiàn)場的技術(shù)問題:
1.項(xiàng)目階段，按照項(xiàng)目經(jīng)理的要求，和客戶與供應(yīng)商進(jìn)行技術(shù)交流。
2.按照pms流程，協(xié)調(diào)項(xiàng)目制造團(tuán)隊(duì)完成各項(xiàng)活動和任務(wù)。
3.通過與產(chǎn)品工程師的合作確保產(chǎn)品設(shè)計(jì)的基于現(xiàn)有技術(shù)可制造性。
4.確保制造的可行性，協(xié)調(diào)手工樣件制作，交付和分析。
5.按照工裝設(shè)備設(shè)計(jì)、評審、驗(yàn)證流程，負(fù)責(zé)產(chǎn)品、工裝、設(shè)備設(shè)計(jì)，并改進(jìn)以降低成本、
6.檢查關(guān)鍵工位制造過程的品質(zhì)，指導(dǎo)或調(diào)整工藝參數(shù)并進(jìn)行改進(jìn)、效果確認(rèn)。
7.按照公司文件要求，負(fù)責(zé)工藝文件的更新，確保工藝文件的可操作性，量產(chǎn)文件更新、變更及管理(變更、回收、作廢)。
8.量產(chǎn)線新儀器、設(shè)備、工裝使用指導(dǎo)，及相關(guān)文件制作。
9.負(fù)責(zé)bmw項(xiàng)目、生產(chǎn)問題解決，協(xié)助編制8d報(bào)告等。
10.技術(shù)支持方向:支持公司整體產(chǎn)線布局及產(chǎn)能的規(guī)劃。
要求:
1.熟悉項(xiàng)目管理體系熟悉iatf16949/pms管理體系
2.熟悉沖壓、注塑、cnc、焊接工藝及設(shè)備原理;
3.能及時預(yù)見及處理生產(chǎn)過程問題，并落實(shí)對策;
4.能夠獨(dú)立主導(dǎo)制造過程問題的分析和并予以解決;
5.具有項(xiàng)目、產(chǎn)品開發(fā)、流程設(shè)計(jì)、生產(chǎn)實(shí)踐經(jīng)驗(yàn);
6.熟悉汽車行業(yè)五大工具:apqp、pfmea、ppap、spc、msa
7.熟悉質(zhì)量問題解決方法，如5why、8d、pdca等
8.主要協(xié)同歐洲團(tuán)隊(duì)工作，英文熟練，可作為工作語言交流
9.抗壓能力強(qiáng)，有做過bmw項(xiàng)目經(jīng)理者優(yōu)先考慮。 作為項(xiàng)目團(tuán)隊(duì)核心成員和工藝開發(fā)團(tuán)隊(duì)主管，負(fù)責(zé)項(xiàng)目所有制造方面技術(shù)工作，從報(bào)價階段開始直到量產(chǎn)后相關(guān)工作，支持生產(chǎn)現(xiàn)場，解決現(xiàn)場的技術(shù)問題:
1.項(xiàng)目階段，按照項(xiàng)目經(jīng)理的要求，和客戶與供應(yīng)商進(jìn)行技術(shù)交流。
2.按照pms流程，協(xié)調(diào)項(xiàng)目制造團(tuán)隊(duì)完成各項(xiàng)活動和任務(wù)。
3.通過與產(chǎn)品工程師的合作確保產(chǎn)品設(shè)計(jì)的基于現(xiàn)有技術(shù)可制造性。
4.確保制造的可行性，協(xié)調(diào)手工樣件制作，交付和分析。
5.按照工裝設(shè)備設(shè)計(jì)、評審、驗(yàn)證流程，負(fù)責(zé)產(chǎn)品、工裝、設(shè)備設(shè)計(jì)，并改進(jìn)以降低成本、
6.檢查關(guān)鍵工位制造過程的品質(zhì)，指導(dǎo)或調(diào)整工藝參數(shù)并進(jìn)行改進(jìn)、效果確認(rèn)。
7.按照公司文件要求，負(fù)責(zé)工藝文件的更新，確保工藝文件的可操作性，量產(chǎn)文件更新、變更及管理(變更、回收、作廢)。
8.量產(chǎn)線新儀器、設(shè)備、工裝使用指導(dǎo)，及相關(guān)文件制作。
9.負(fù)責(zé)bmw項(xiàng)目、生產(chǎn)問題解決，協(xié)助編制8d報(bào)告等。
10.技術(shù)支持方向:支持公司整體產(chǎn)線布局及產(chǎn)能的規(guī)劃。
要求:
1.熟悉項(xiàng)目管理體系熟悉iatf16949/pms管理體系
2.熟悉沖壓、注塑、cnc、焊接工藝及設(shè)備原理;
3.能及時預(yù)見及處理生產(chǎn)過程問題，并落實(shí)對策;
4.能夠獨(dú)立主導(dǎo)制造過程問題的分析和并予以解決;
5.具有項(xiàng)目、產(chǎn)品開發(fā)、流程設(shè)計(jì)、生產(chǎn)實(shí)踐經(jīng)驗(yàn);
6.熟悉汽車行業(yè)五大工具:apqp、pfmea、ppap、spc、msa
7.熟悉質(zhì)量問題解決方法，如5why、8d、pdca等
8.主要協(xié)同歐洲團(tuán)隊(duì)工作，英文熟練，可作為工作語言交流
9.抗壓能力強(qiáng)，有做過bmw項(xiàng)目經(jīng)理者優(yōu)先考慮。
項(xiàng)目工藝工程師崗位
第9篇 工藝項(xiàng)目工程師崗位職責(zé)
項(xiàng)目總工程師(水處理工藝方向) 廣州資源投資集團(tuán) 廣州資源投資集團(tuán)有限公司,廣州資源投資集團(tuán) 崗位職責(zé):
1、在總工室的領(lǐng)導(dǎo)下開展各項(xiàng)工作,負(fù)責(zé)組織管理公司的污水處理工藝方面施工技術(shù)與質(zhì)量管理的日常工作;
2、根據(jù)分管工作需要,進(jìn)行團(tuán)隊(duì)建設(shè),保持團(tuán)隊(duì)的團(tuán)結(jié)、穩(wěn)定、向上,對下屬人員的工作結(jié)果負(fù)責(zé);
3、建立公司的施工技術(shù)、質(zhì)量管理體系,并對各項(xiàng)目施工過程中的施工技術(shù)、質(zhì)量進(jìn)行有效管理;
4、組織編制公司的工程技術(shù)管理辦法;制定項(xiàng)目部的技術(shù)管理辦法,并監(jiān)督執(zhí)行;
5、對項(xiàng)目部提交的施工技術(shù)方案進(jìn)行審定和交底,指導(dǎo)并審核項(xiàng)目重大工程變更;
6、負(fù)責(zé)組織對項(xiàng)目質(zhì)量事故的調(diào)查、處理;
7、定期組織對公司建設(shè)項(xiàng)目進(jìn)行檢查督導(dǎo),對項(xiàng)目的技術(shù)管理、質(zhì)量、資料負(fù)直接領(lǐng)導(dǎo)責(zé)任。
8、完成領(lǐng)導(dǎo)安排的其它事務(wù)。
任職要求:
1、大學(xué)本科及以上學(xué)歷,給排水、環(huán)境工程、電氣自動化、土木工程、園林景觀等相關(guān)專業(yè);具有水生態(tài)修復(fù)、市政工程、水利工程等專業(yè)知識;
2、具有大型國企、央企施工類企業(yè)項(xiàng)目總工或總工室工作經(jīng)驗(yàn)的優(yōu)先考慮;
3、具備市政給排水專業(yè)管網(wǎng)工程設(shè)計(jì)、常規(guī)污水處理設(shè)計(jì)、其它污水處理工藝設(shè)計(jì)、生態(tài)修復(fù)工程設(shè)計(jì)經(jīng)驗(yàn);
4、具備優(yōu)秀的項(xiàng)目組織能力,優(yōu)秀的交流表達(dá)和綜合協(xié)調(diào)能力,能夠?qū)Ω髟O(shè)計(jì)階段出現(xiàn)的較為復(fù)雜的問題進(jìn)行預(yù)判、協(xié)調(diào)和解決;
5、具備獨(dú)立完成方案設(shè)計(jì)、可研、初設(shè)、施工圖設(shè)計(jì)的能力,具有很好的技術(shù)管理經(jīng)驗(yàn),能帶領(lǐng)設(shè)計(jì)團(tuán)隊(duì)進(jìn)行高效率工作;
6、具有中/高專業(yè)技術(shù)職稱或注冊類資格證書者優(yōu)先。
第10篇 疫苗工藝項(xiàng)目經(jīng)理崗位職責(zé)
1.負(fù)責(zé)新疫苗工藝技術(shù)的研發(fā)工作。
2.對生物藥品生產(chǎn)環(huán)節(jié)的工藝提高、劑型改進(jìn)和產(chǎn)品升級提供技術(shù)支持。
3.根據(jù)項(xiàng)目建立并管理研發(fā)團(tuán)隊(duì),組織實(shí)施日?？蒲泄芾怼?/p>
第11篇 工藝項(xiàng)目工程師崗位職責(zé)工藝項(xiàng)目工程師職責(zé)任職要求
工藝項(xiàng)目工程師崗位職責(zé)
工藝項(xiàng)目工程師 1.integrate and co-ordinate with the design institutes conception phase till the completion of the project.
從概念設(shè)計(jì)到項(xiàng)目完成，協(xié)同設(shè)計(jì)院進(jìn)行工作。
2.assist in preparing， developing the front-end engineering work of the process， piping and etc.
準(zhǔn)備和配合完成工藝、管道等的前期設(shè)計(jì)工作。
3.assist in preparation of basic conceptual design， p&i diagrams for the small and medium size project.
協(xié)助完成中小型項(xiàng)目的概念設(shè)計(jì)和p&id.
4.prepare and review design specification， technical data sheet， drawings for onshore and offshore facilities.
準(zhǔn)備并審核陸域和海域項(xiàng)目的設(shè)計(jì)階段的技術(shù)規(guī)格書、數(shù)據(jù)表、圖紙。
5.site planning， co-ordination， supervision and inspection of tankage and piping work to ensure e_ecution safely in good quality. monitor of work progress and also to ensure good quality of the design and construction of the project that comply with the required standards
現(xiàn)場計(jì)劃、協(xié)調(diào)、督促和檢查有關(guān)儲罐和管道的施工，并監(jiān)督設(shè)計(jì)和施工的進(jìn)度及質(zhì)量符合相關(guān)的標(biāo)準(zhǔn)和規(guī)范。
6.ensure vpm and vopak way compliance during design phase.
在設(shè)計(jì)階段遵循vpm 和vapok way的規(guī)定.
7.assist in carrying out site piping， mechanical， tankage inspection /acceptance work.
協(xié)助進(jìn)行壓力管道、儲罐、機(jī)械系統(tǒng)等的檢查和驗(yàn)收。
8.assist in preparing quotations to support the commercial activities.
提供預(yù)算報(bào)價，協(xié)助支持商務(wù)活動。
9.assist in preparation of tendering documents as and what needed.
協(xié)助準(zhǔn)備項(xiàng)目的招投標(biāo)文件。
skills & knowledge:
技能知識:
-chemical process or petrochemical or relevant engineering.
化工工藝或石油化工及相關(guān)工程專業(yè)。
-6+ years related e_perience in chemical industry or petrochemical industry， especially in terminal field.
6年以上化學(xué)工業(yè)或者石化工業(yè)的相關(guān)經(jīng)驗(yàn)，尤其在罐區(qū)方面。
-familiar with relevant domestic/international standards， especially domestic.
熟悉相關(guān)國際/國內(nèi)規(guī)范和標(biāo)準(zhǔn)。
-good verbal and written communication skill， both in english and mandarin.
在英語和普通話方面，有良好的口語和書面溝通能力。
-skilled in office pc application programs， especially in auto-cad.
熟練辦公室計(jì)算機(jī)應(yīng)用程序，尤其是auto-cad。
-capable of independently analysis， handling problems.
能獨(dú)立分析和解決問題。
-hardworking and able to work under pressure.
能承受較大的工作壓力。
會化工工藝計(jì)算(管道流體，泵的揚(yáng)程等，畫圖軟件比較熟練，英語讀寫較好) 1.integrate and co-ordinate with the design institutes conception phase till the completion of the project.
從概念設(shè)計(jì)到項(xiàng)目完成，協(xié)同設(shè)計(jì)院進(jìn)行工作。
2.assist in preparing， developing the front-end engineering work of the process， piping and etc.
準(zhǔn)備和配合完成工藝、管道等的前期設(shè)計(jì)工作。
3.assist in preparation of basic conceptual design， p&i diagrams for the small and medium size project.
協(xié)助完成中小型項(xiàng)目的概念設(shè)計(jì)和p&id.
4.prepare and review design specification， technical data sheet， drawings for onshore and offshore facilities.
準(zhǔn)備并審核陸域和海域項(xiàng)目的設(shè)計(jì)階段的技術(shù)規(guī)格書、數(shù)據(jù)表、圖紙。
5.site planning， co-ordination， supervision and inspection of tankage and piping work to ensure e_ecution safely in good quality. monitor of work progress and also to ensure good quality of the design and construction of the project that comply with the required standards
現(xiàn)場計(jì)劃、協(xié)調(diào)、督促和檢查有關(guān)儲罐和管道的施工，并監(jiān)督設(shè)計(jì)和施工的進(jìn)度及質(zhì)量符合相關(guān)的標(biāo)準(zhǔn)和規(guī)范。
6.ensure vpm and vopak way compliance during design phase.
在設(shè)計(jì)階段遵循vpm 和vapok way的規(guī)定.
7.assist in carrying out site piping， mechanical， tankage inspection /acceptance work.
協(xié)助進(jìn)行壓力管道、儲罐、機(jī)械系統(tǒng)等的檢查和驗(yàn)收。
8.assist in preparing quotations to support the commercial activities.
提供預(yù)算報(bào)價，協(xié)助支持商務(wù)活動。
9.assist in preparation of tendering documents as and what needed.
協(xié)助準(zhǔn)備項(xiàng)目的招投標(biāo)文件。
skills & knowledge:
技能知識:
-chemical process or petrochemical or relevant engineering.
化工工藝或石油化工及相關(guān)工程專業(yè)。
-6+ years related e_perience in chemical industry or petrochemical industry， especially in terminal field.
6年以上化學(xué)工業(yè)或者石化工業(yè)的相關(guān)經(jīng)驗(yàn)，尤其在罐區(qū)方面。
-familiar with relevant domestic/international standards， especially domestic.
熟悉相關(guān)國際/國內(nèi)規(guī)范和標(biāo)準(zhǔn)。
-good verbal and written communication skill， both in english and mandarin.
在英語和普通話方面，有良好的口語和書面溝通能力。
-skilled in office pc application programs， especially in auto-cad.
熟練辦公室計(jì)算機(jī)應(yīng)用程序，尤其是auto-cad。
-capable of independently analysis， handling problems.
能獨(dú)立分析和解決問題。
-hardworking and able to work under pressure.
能承受較大的工作壓力。
會化工工藝計(jì)算(管道流體，泵的揚(yáng)程等，畫圖軟件比較熟練，英語讀寫較好)
第12篇 項(xiàng)目工藝崗位職責(zé)
項(xiàng)目總工程師(水處理工藝方向) 廣州資源投資集團(tuán) 廣州資源投資集團(tuán)有限公司,廣州資源投資集團(tuán) 崗位職責(zé):
1、在總工室的領(lǐng)導(dǎo)下開展各項(xiàng)工作,負(fù)責(zé)組織管理公司的污水處理工藝方面施工技術(shù)與質(zhì)量管理的日常工作;
2、根據(jù)分管工作需要,進(jìn)行團(tuán)隊(duì)建設(shè),保持團(tuán)隊(duì)的團(tuán)結(jié)、穩(wěn)定、向上,對下屬人員的工作結(jié)果負(fù)責(zé);
3、建立公司的施工技術(shù)、質(zhì)量管理體系,并對各項(xiàng)目施工過程中的施工技術(shù)、質(zhì)量進(jìn)行有效管理;
4、組織編制公司的工程技術(shù)管理辦法;制定項(xiàng)目部的技術(shù)管理辦法,并監(jiān)督執(zhí)行;
5、對項(xiàng)目部提交的施工技術(shù)方案進(jìn)行審定和交底,指導(dǎo)并審核項(xiàng)目重大工程變更;
6、負(fù)責(zé)組織對項(xiàng)目質(zhì)量事故的調(diào)查、處理;
7、定期組織對公司建設(shè)項(xiàng)目進(jìn)行檢查督導(dǎo),對項(xiàng)目的技術(shù)管理、質(zhì)量、資料負(fù)直接領(lǐng)導(dǎo)責(zé)任。
8、完成領(lǐng)導(dǎo)安排的其它事務(wù)。
任職要求:
1、大學(xué)本科及以上學(xué)歷,給排水、環(huán)境工程、電氣自動化、土木工程、園林景觀等相關(guān)專業(yè);具有水生態(tài)修復(fù)、市政工程、水利工程等專業(yè)知識;
2、具有大型國企、央企施工類企業(yè)項(xiàng)目總工或總工室工作經(jīng)驗(yàn)的優(yōu)先考慮;
3、具備市政給排水專業(yè)管網(wǎng)工程設(shè)計(jì)、常規(guī)污水處理設(shè)計(jì)、其它污水處理工藝設(shè)計(jì)、生態(tài)修復(fù)工程設(shè)計(jì)經(jīng)驗(yàn);
4、具備優(yōu)秀的項(xiàng)目組織能力,優(yōu)秀的交流表達(dá)和綜合協(xié)調(diào)能力,能夠?qū)Ω髟O(shè)計(jì)階段出現(xiàn)的較為復(fù)雜的問題進(jìn)行預(yù)判、協(xié)調(diào)和解決;
5、具備獨(dú)立完成方案設(shè)計(jì)、可研、初設(shè)、施工圖設(shè)計(jì)的能力,具有很好的技術(shù)管理經(jīng)驗(yàn),能帶領(lǐng)設(shè)計(jì)團(tuán)隊(duì)進(jìn)行高效率工作;
6、具有中/高專業(yè)技術(shù)職稱或注冊類資格證書者優(yōu)先。
第13篇 化工工藝項(xiàng)目崗位職責(zé)任職要求
化工工藝項(xiàng)目崗位職責(zé)
化工工藝技術(shù)員(蒲城項(xiàng)目部) 陜西煤業(yè)化工技術(shù)研究院有限責(zé)任公司 陜西煤業(yè)化工技術(shù)研究院有限責(zé)任公司 1、進(jìn)行各試驗(yàn)裝置的調(diào)試、開車、運(yùn)行等工作;
2、協(xié)助進(jìn)行工藝包編制、試驗(yàn)過程優(yōu)化等工作。
任職要求:
1、大型化工企業(yè)內(nèi)從事專業(yè)相關(guān)工作5年及以上;
2、具有副操、主操、技術(shù)員等崗位工作經(jīng)歷。
化工工藝項(xiàng)目崗位
第14篇 項(xiàng)目生產(chǎn)工藝崗位職責(zé)
有機(jī)肥生產(chǎn)工藝-項(xiàng)目經(jīng)理 臨沂金豐公社農(nóng)業(yè)服務(wù)有限公司 臨沂金豐公社農(nóng)業(yè)服務(wù)有限公司,金豐 職責(zé)描述:
1.根據(jù)企業(yè)年度戰(zhàn)略計(jì)劃或者要求制定生產(chǎn)工藝研發(fā)任務(wù)計(jì)劃,報(bào)領(lǐng)導(dǎo)審批后組織人員實(shí)施;
2.監(jiān)督生產(chǎn)工藝研發(fā)計(jì)劃的具體實(shí)施情況,根據(jù)實(shí)際的情況對計(jì)劃進(jìn)行合適的調(diào)整;
3.參與研發(fā)試驗(yàn),并根據(jù)實(shí)際研發(fā)需要改進(jìn)生產(chǎn)設(shè)備;
4.幫助研發(fā)成員解決實(shí)際研發(fā)中出現(xiàn)的問題;
5.新工藝研發(fā)成功和首件產(chǎn)品制作后,組織和協(xié)調(diào)成員負(fù)責(zé)首件成品和樣品的確認(rèn)工作;
6.組織人員制定工藝標(biāo)準(zhǔn)、操作規(guī)范等技術(shù)文件,并監(jiān)督實(shí)施;
7.不斷的改善工藝技術(shù),降低公司成本;
8.為生產(chǎn)線和采購部門提供必要的技術(shù)支持,保證生產(chǎn)線的正常運(yùn)作和采購部門的采購任務(wù)順利完成;
9.與產(chǎn)品和質(zhì)量部門的人員協(xié)作,對產(chǎn)品質(zhì)量問題進(jìn)行分析并解決;
10.對生產(chǎn)工藝研發(fā)成員進(jìn)行技術(shù)指導(dǎo)和培訓(xùn),提高成員的工藝水平和能力。
任職要求:
1.熟悉生物有機(jī)肥生產(chǎn)工藝與技術(shù),有豐富的工作經(jīng)驗(yàn)
2.具備一定的技術(shù)管理和人員管理能力;
3.工作認(rèn)真,具有高度的責(zé)任心。
第15篇 工藝開發(fā)項(xiàng)目崗位職責(zé)任職要求
工藝開發(fā)項(xiàng)目崗位職責(zé)
制藥工藝開發(fā)工程師/項(xiàng)目負(fù)責(zé)人 深圳市樂土生命科技投資有限公司 深圳市樂土生命科技投資有限公司 1、 領(lǐng)導(dǎo)部門團(tuán)隊(duì)承擔(dān)各生物藥項(xiàng)目生產(chǎn)工藝研究和開發(fā)，關(guān)于細(xì)胞培養(yǎng)工藝開發(fā)、蛋白純化及超濾工藝開發(fā)等。
2、 負(fù)責(zé)項(xiàng)目由開發(fā)階段向中試生產(chǎn)的工藝技術(shù)轉(zhuǎn)移，協(xié)調(diào)解決中試放大中碰到的工藝技術(shù)問題。
3、生物醫(yī)藥項(xiàng)目立項(xiàng)、可行性分析論證及組織實(shí)施。
4、醫(yī)藥研發(fā)信息資料查閱及收集。
5、生物醫(yī)藥研發(fā)實(shí)驗(yàn)室設(shè)備儀器使用、操作及簡單維護(hù)。
6、制定部門或項(xiàng)目人員、設(shè)備及財(cái)務(wù)預(yù)算等。
任職要求:
1、碩士以上學(xué)歷，生物技術(shù)或藥物學(xué)相關(guān)專業(yè);3-5年制藥公司研發(fā)崗位相關(guān)經(jīng)驗(yàn)，有項(xiàng)目管理經(jīng)驗(yàn)優(yōu)先;
2、有單克隆抗體制備、多肽純化等項(xiàng)目經(jīng)驗(yàn)的優(yōu)先考慮;精通生物制藥相關(guān)生產(chǎn)工藝的開發(fā)，熟悉生物制藥生產(chǎn)過程，有一定的gmp經(jīng)驗(yàn);
3、動手能力強(qiáng)。頭腦靈活，溝通能力強(qiáng);
4、能夠查閱、調(diào)研英文信息資料;
5、具有較強(qiáng)的團(tuán)隊(duì)協(xié)作精神。
