- 目錄
崗位職責(zé)是什么
醫(yī)用耗材崗位，是醫(yī)療行業(yè)中不可或缺的一環(huán)，主要負(fù)責(zé)醫(yī)療機(jī)構(gòu)內(nèi)部醫(yī)用耗材的采購、管理、分發(fā)和監(jiān)控等工作。這個(gè)崗位的工作人員需要確保醫(yī)療設(shè)備和一次性用品的質(zhì)量與供應(yīng)，以滿足臨床診療的需求，保障患者安全和醫(yī)療服務(wù)質(zhì)量。
崗位職責(zé)要求
1. 專業(yè)知識：具備醫(yī)學(xué)背景知識，了解各類醫(yī)用耗材的特性和用途。
2. 供應(yīng)鏈管理：掌握醫(yī)用耗材的采購流程，能有效控制庫存，避免浪費(fèi)。
3. 質(zhì)量把控：嚴(yán)格遵守醫(yī)療法規(guī)，確保所購耗材符合國家質(zhì)量和安全標(biāo)準(zhǔn)。
4. 溝通協(xié)調(diào)：與供應(yīng)商、臨床科室保持良好溝通，及時(shí)響應(yīng)需求變化。
5. 數(shù)據(jù)管理：熟練運(yùn)用信息系統(tǒng)，準(zhǔn)確記錄和分析耗材使用情況。
6. 成本意識：在保證醫(yī)療質(zhì)量的前提下，注重經(jīng)濟(jì)效益，合理控制采購成本。
崗位職責(zé)描述
醫(yī)用耗材崗位的工作日常涵蓋了多個(gè)方面。在采購階段，需要評估供應(yīng)商資質(zhì)，比較價(jià)格、性能，簽訂合同，并跟蹤訂單執(zhí)行情況。在庫存管理中，需定期盤點(diǎn)，預(yù)警低庫存，避免耗材短缺影響醫(yī)療服務(wù)。該崗位人員需參與新設(shè)備或耗材的引進(jìn)評估，確保其適應(yīng)臨床需求。在耗材分發(fā)環(huán)節(jié)，應(yīng)按照規(guī)定程序，確保正確無誤地發(fā)放到各科室。此外，還要定期分析耗材使用數(shù)據(jù)，為醫(yī)院管理層提供決策依據(jù)，優(yōu)化資源配置。
有哪些內(nèi)容
1. 耗材采購：制定采購計(jì)劃，篩選優(yōu)質(zhì)供應(yīng)商，談判合同條款，監(jiān)督交貨質(zhì)量。
2. 庫存控制：實(shí)施庫存管理策略，如先進(jìn)先出，定期盤點(diǎn)，預(yù)防過期或損壞。
3. 質(zhì)量檢查：對入庫耗材進(jìn)行驗(yàn)收，確保符合標(biāo)準(zhǔn)，處理不合格品。
4. 耗材分發(fā)：根據(jù)臨床需求，及時(shí)、準(zhǔn)確分發(fā)耗材，記錄使用情況。
5. 數(shù)據(jù)分析：收集、整理耗材使用數(shù)據(jù)，進(jìn)行統(tǒng)計(jì)分析，提供改進(jìn)建議。
6. 合規(guī)性維護(hù)：熟悉醫(yī)療法規(guī)，確保耗材管理過程符合法律法規(guī)要求。
7. 應(yīng)急處理：應(yīng)對突發(fā)的耗材短缺，制定應(yīng)急方案，保障醫(yī)療服務(wù)連續(xù)性。
8. 培訓(xùn)與教育：參與或組織醫(yī)用耗材使用培訓(xùn)，提高醫(yī)護(hù)人員的正確使用意識。
醫(yī)用耗材崗位在醫(yī)療體系中扮演著重要角色，不僅需要專業(yè)知識，還需要良好的管理能力和服務(wù)意識，以確保醫(yī)療耗材的有效利用，為患者提供安全、高效的醫(yī)療服務(wù)。
醫(yī)用耗材崗位職責(zé)范文
第1篇 醫(yī)用耗材銷售代表崗位職責(zé)
崗位職責(zé):
1、負(fù)責(zé)公司主營產(chǎn)品(中國總代,進(jìn)口同類產(chǎn)品無競品)在二級和三級醫(yī)院皮膚科的銷售和推廣工作;
2、能夠完成公司制定的銷售任務(wù)和目標(biāo);
3、負(fù)責(zé)轄區(qū)醫(yī)院的開發(fā)和學(xué)術(shù)推廣,解答學(xué)術(shù)問題,與客戶保持良好溝通;
4、及時(shí)了解、收集整理、分析、反饋市場信息;
5、跟進(jìn)銷售回款,維持良性帳期。
任職資格:
1、統(tǒng)招?？萍耙陨蠈W(xué)歷,醫(yī)學(xué)、生物、檢驗(yàn)等相關(guān)專業(yè);
2、1年以上銷售工作經(jīng)驗(yàn),有醫(yī)藥、耗材、醫(yī)美儀器相關(guān)銷售經(jīng)驗(yàn)者優(yōu)先;
3、有良好的溝通能力、學(xué)習(xí)能力、執(zhí)行力。
第2篇 醫(yī)用耗材崗位職責(zé)
quality director china key requirements
minimum of 10 years’ e_perience in quality assurance in a relevant regulated environment (medical devices, biocides, or pharmaceuticals products).
university degree in science or equivilant discipline
must have a working knowledge of medical devices or biocides regulations.
3-5 years management of iso9001 or iso13485 quality management systems to drive business performance and efficiency and drive supplier performance.
at least 3-5 years leading, managing and developing professional teams.
e_perience of working effectively in an entrepreneurial, fast paced international organisation.
managing supplier performance within a quality management system
e_perience of operating in an international environment and managing a variety of market-specific regulatory frameworks. (desirable)
knowledge / e_perience with risk management and us good manufacturing practice, medical devices, biocides, pharmaceuticals, cosmetics, detergents, personal protective equipment, electromagnetic compatibility. (desirable)
must hold a valid driving licence.
who we are looking for
strong quality management e_perience.
strong ability to influence effectively both internally and with e_ternal suppliers while maintaining good working relationships.
previous proven e_perience in managing and developing staff members with variable levels of e_perience and e_pertise.
ability to communicate clearly and concisely internally and with government authorities and registrars
knowledge of relevant regulations, standards and compliance requirements with respect to the company products whether directly or through associates and contacts.
previous e_perience working within a fast-paced entrepreneurial business, supporting the development of a rich product pipeline.
strong international outlook and have e_perience of working in a multicultural environment.
demonstrate a strong blend of technical and interpersonal skills that you will use to develop and influence relationships to enhance and maintain our position in a competitive environment.
e_cellent english language skills written/ verbal.
(_ including medical devices, biocides, pharmaceuticals, cosmetics, detergents, personal protective equipment, electromagnetic compatibility) competitive salary, car, performance bonus and benefits key requirements
minimum of 10 years’ e_perience in quality assurance in a relevant regulated environment (medical devices, biocides, or pharmaceuticals products).
university degree in science or equivilant discipline
must have a working knowledge of medical devices or biocides regulations.
3-5 years management of iso9001 or iso13485 quality management systems to drive business performance and efficiency and drive supplier performance.
at least 3-5 years leading, managing and developing professional teams.
e_perience of working effectively in an entrepreneurial, fast paced international organisation.
managing supplier performance within a quality management system
e_perience of operating in an international environment and managing a variety of market-specific regulatory frameworks. (desirable)
knowledge / e_perience with risk management and us good manufacturing practice, medical devices, biocides, pharmaceuticals, cosmetics, detergents, personal protective equipment, electromagnetic compatibility. (desirable)
must hold a valid driving licence.
who we are looking for
strong quality management e_perience.
strong ability to influence effectively both internally and with e_ternal suppliers while maintaining good working relationships.
previous proven e_perience in managing and developing staff members with variable levels of e_perience and e_pertise.
ability to communicate clearly and concisely internally and with government authorities and registrars
knowledge of relevant regulations, standards and compliance requirements with respect to the company products whether directly or through associates and contacts.
previous e_perience working within a fast-paced entrepreneurial business, supporting the development of a rich product pipeline.
strong international outlook and have e_perience of working in a multicultural environment.
demonstrate a strong blend of technical and interpersonal skills that you will use to develop and influence relationships to enhance and maintain our position in a competitive environment.
e_cellent english language skills written/ verbal.
(_ including medical devices, biocides, pharmaceuticals, cosmetics, detergents, personal protective equipment, electromagnetic compatibility)
第3篇 醫(yī)用耗材產(chǎn)品崗位職責(zé)
崗位職責(zé):
1.在轄區(qū)內(nèi)醫(yī)院進(jìn)行公司產(chǎn)品的臨床推廣銷售,完成公司制定的銷售任務(wù);
2.根據(jù)需要拜訪醫(yī)護(hù)人員,向客戶推廣產(chǎn)品,不斷提高產(chǎn)品市場份額;
3.開拓潛在的醫(yī)院渠道客戶,并對既有的客戶進(jìn)行維護(hù);
4.充分了解市場狀態(tài),及時(shí)向上級主管反映競爭產(chǎn)品的情況及市場活動(dòng)、提出合理化建議。
任職要求:
1.大專及以上學(xué)歷,臨床醫(yī)學(xué)、醫(yī)療器械、藥學(xué)、護(hù)理學(xué)等專業(yè)畢業(yè)者優(yōu)先;
2.兩年以上相關(guān)工作經(jīng)驗(yàn),年齡22~37歲以內(nèi);
3.有醫(yī)療器械、耗材銷售經(jīng)驗(yàn)者優(yōu)先;
4.熟悉醫(yī)院工作流程,能夠獨(dú)立開發(fā)客戶,熱愛醫(yī)療器械耗材銷售工作者優(yōu)先;
5.適應(yīng)省內(nèi)經(jīng)常出差,品貌端正,誠實(shí)可靠,有良好的溝通技巧,吃苦耐勞,責(zé)任心強(qiáng),有團(tuán)隊(duì)合作精神。
待遇:
1.基本工資+績效+獎(jiǎng)金+福利(餐補(bǔ)+節(jié)假日補(bǔ)貼+出差補(bǔ)貼+交通電話補(bǔ)助+高溫、取暖費(fèi));
2.彈性工作制,五險(xiǎn)一金,每年體檢,團(tuán)隊(duì)活動(dòng),一年后有帶薪年假。
我們熱忱歡迎有志之士加入!
第4篇 醫(yī)用耗材銷售經(jīng)理崗位職責(zé)
1、勤奮敬業(yè),執(zhí)行力強(qiáng),態(tài)度積極不抱怨,從內(nèi)心喜歡這個(gè)職業(yè),有團(tuán)隊(duì)責(zé)任感!
2、三年以上同崗位銷售經(jīng)驗(yàn),有全省銷售網(wǎng)絡(luò)和臨床經(jīng)驗(yàn)者優(yōu)先。
3、可以適應(yīng)出差。
第5篇 醫(yī)用耗材銷售崗位職責(zé)
醫(yī)用耗材銷售主管(西南大區(qū)) 巨鯊 南京巨鯊顯示科技有限公司,巨鯊,巨鯊醫(yī)療,巨鯊商貿(mào),巨鯊 base地為成都。
崗位職責(zé):
1、負(fù)責(zé)公司medrad耗材產(chǎn)品在西南,主要在四川的業(yè)務(wù);
3、執(zhí)行公司各項(xiàng)銷售政策,完成季度、年度銷售任務(wù);
4、輔導(dǎo)直接下屬并協(xié)助大區(qū)總監(jiān)完成銷售團(tuán)隊(duì)的建設(shè)發(fā)展。
任職要求:
1、本科及以上學(xué)歷;
2、有至少3年醫(yī)療行業(yè)相關(guān)工作經(jīng)驗(yàn),有外企相關(guān)工作經(jīng)驗(yàn)者優(yōu)先;
3、具備團(tuán)隊(duì)管理經(jīng)驗(yàn),擅長團(tuán)隊(duì)輔導(dǎo),能夠帶領(lǐng)團(tuán)隊(duì)達(dá)成銷售目標(biāo);
4、開拓性的思路,良好的內(nèi)外溝通技能和執(zhí)行力;
5、為人正直,富有激情,能承受工作壓力,能夠適應(yīng)出差。
