崗位職責(zé)是什么
制藥行業(yè)崗位職責(zé)涵蓋了從研發(fā)、生產(chǎn)到質(zhì)量控制、市場(chǎng)營(yíng)銷等多個(gè)環(huán)節(jié)，每個(gè)崗位都有其獨(dú)特的任務(wù)和責(zé)任，共同致力于確保藥品的安全、有效和合規(guī)。
崗位職責(zé)要求
1. 熟悉相關(guān)法規(guī)：要求員工對(duì)國(guó)內(nèi)外制藥行業(yè)的法律法規(guī)有深入理解，包括gmp、glp、gcp等相關(guān)標(biāo)準(zhǔn)。
2. 技術(shù)專長(zhǎng)：各崗位需具備相應(yīng)的專業(yè)技能，如化學(xué)、生物學(xué)、藥理學(xué)知識(shí)，以及實(shí)驗(yàn)操作、數(shù)據(jù)分析能力。
3. 細(xì)心嚴(yán)謹(jǐn)：制藥行業(yè)對(duì)精度和準(zhǔn)確性要求極高，因此員工需要具備細(xì)心、嚴(yán)謹(jǐn)?shù)墓ぷ鲬B(tài)度。
4. 團(tuán)隊(duì)協(xié)作：工作常涉及跨部門合作，良好的溝通協(xié)調(diào)能力至關(guān)重要。
5. 持續(xù)學(xué)習(xí)：隨著科技發(fā)展，需要不斷更新知識(shí)，適應(yīng)新的研究方法和技術(shù)。
崗位職責(zé)描述
1. 研發(fā)工程師：負(fù)責(zé)新藥的研發(fā)，包括藥物設(shè)計(jì)、合成、篩選及臨床前試驗(yàn)，確保新藥的安全性和有效性。
2. 生產(chǎn)主管：管理生產(chǎn)線，確保藥品生產(chǎn)符合gmp標(biāo)準(zhǔn)，保證產(chǎn)品質(zhì)量，同時(shí)優(yōu)化生產(chǎn)流程，提高效率。
3. 質(zhì)量控制專員：進(jìn)行原料、中間體和成品的質(zhì)量檢驗(yàn)，確保符合質(zhì)量標(biāo)準(zhǔn)，并對(duì)異常情況進(jìn)行調(diào)查和處理。
4. 注冊(cè)專員：負(fù)責(zé)藥品注冊(cè)申請(qǐng)，跟蹤審批進(jìn)度，確保產(chǎn)品合規(guī)上市。
5. 市場(chǎng)營(yíng)銷經(jīng)理：分析市場(chǎng)趨勢(shì)，制定銷售策略，推廣公司產(chǎn)品，同時(shí)處理客戶反饋，提升品牌形象。
有哪些內(nèi)容
1. 制定并執(zhí)行研發(fā)計(jì)劃：包括新藥設(shè)計(jì)、實(shí)驗(yàn)室研究、臨床試驗(yàn)等階段，確保項(xiàng)目按期完成。
2. 生產(chǎn)管理：監(jiān)控生產(chǎn)過程，解決生產(chǎn)中出現(xiàn)的問題，確保藥品批次間的一致性。
3. 質(zhì)量管理體系維護(hù)：建立和完善質(zhì)量控制流程，進(jìn)行內(nèi)部審核，確保符合行業(yè)規(guī)范。
4. 法規(guī)遵循：跟蹤法規(guī)動(dòng)態(tài)，及時(shí)調(diào)整公司政策和操作程序，防止違規(guī)風(fēng)險(xiǎn)。
5. 市場(chǎng)調(diào)研：收集競(jìng)品信息，分析客戶需求，為產(chǎn)品定位和定價(jià)提供依據(jù)。
6. 客戶關(guān)系管理：維護(hù)客戶關(guān)系，處理客戶投訴，提升客戶滿意度。
7. 技術(shù)支持：為銷售團(tuán)隊(duì)提供技術(shù)支持，解答客戶關(guān)于產(chǎn)品特性和應(yīng)用的問題。
8. 培訓(xùn)與發(fā)展：組織內(nèi)部培訓(xùn)，提升員工的專業(yè)技能和法規(guī)知識(shí)，推動(dòng)團(tuán)隊(duì)成長(zhǎng)。
制藥行業(yè)崗位職責(zé)的核心在于對(duì)質(zhì)量的堅(jiān)守、法規(guī)的遵循和持續(xù)的創(chuàng)新，每一位員工都是保障公眾健康的重要一環(huán)。
制藥行業(yè)崗位職責(zé)范文
第1篇 制藥行業(yè)銷售崗位職責(zé)
制藥行業(yè)銷售工程師 寶帝流體控制系統(tǒng) 寶帝流體控制系統(tǒng)(上海)有限公司,寶帝,寶帝流體控制系統(tǒng),流體控制系統(tǒng),寶帝 職責(zé)描述:
1、負(fù)責(zé)氣動(dòng)過程閥門,工業(yè)用傳感器類的產(chǎn)品推廣
2、負(fù)責(zé)銷售工作整體運(yùn)作的有效執(zhí)行,完成公司業(yè)績(jī)和達(dá)成預(yù)期市場(chǎng)占有率目標(biāo)
3、開發(fā)區(qū)域內(nèi)及制藥行業(yè)內(nèi)新客戶
4、維護(hù),鞏固,提升與老客戶的關(guān)系
5、熟悉行業(yè)動(dòng)態(tài),提供行業(yè)趨勢(shì)分析,為客戶提供技術(shù)支持,并善于發(fā)現(xiàn)新商機(jī)
任職要求:
1、本科(全日制)及以上;
2、機(jī)械、機(jī)電、機(jī)械自動(dòng)化、電氣自動(dòng)化、儀表自動(dòng)化、化工工程工藝、制藥工程工藝、發(fā)酵等相關(guān)專業(yè)優(yōu)先;
3、3年以上閥門、儀表等相關(guān)產(chǎn)品的銷售經(jīng)驗(yàn),制藥行業(yè)的工程公司、設(shè)備成套商、衛(wèi)生管道相關(guān)工作經(jīng)驗(yàn);
4、制藥行業(yè),尤其是生物制藥、疫苗、血液制品行業(yè)銷售經(jīng)驗(yàn)優(yōu)先。
第2篇 生物制藥行業(yè)崗位職責(zé)
技術(shù)支持工程師(生物制藥行業(yè)) 安諾 杭州安諾過濾器材有限公司,安諾,安諾 崗位職責(zé):
1、負(fù)責(zé)與客戶的技術(shù)交流工作,收集客戶的技術(shù)要求,并進(jìn)行初步分析和分解;
2、負(fù)責(zé)產(chǎn)品應(yīng)用背景評(píng)估和技術(shù)分析,根據(jù)客戶需求和產(chǎn)品性能提供合適的解決方案;
3、負(fù)責(zé)本行業(yè)過濾技術(shù)應(yīng)用前景及市場(chǎng)分析,使產(chǎn)品開發(fā)落地;
4、負(fù)責(zé)解答客戶對(duì)產(chǎn)品使用、投訴等相關(guān)問題;
5、負(fù)責(zé)本行業(yè)的內(nèi)、外技術(shù)交流和培訓(xùn)。
任職要求:
1、生物化工、生物制藥相關(guān)專業(yè)碩士及以上學(xué)歷。
2、具有優(yōu)秀的溝通表達(dá)能力及組織協(xié)調(diào)能力。
3、熟悉原料藥、無菌制劑等產(chǎn)品制造工藝。
4、能配合公司適應(yīng)短期出差。
第3篇 制藥行業(yè)崗位職責(zé)
qa manager-制藥行業(yè) responsibilities:
in charge site quality control, quality system management.
set up the company quality goal and regularly review the status of quality target. train and guide the team to reach functional quality goal.
manage engineers and inspectors team of qa section, coordinate with other dept./team.
define the quality assurance policy and process, lead the implementation of quality assurance models and system that can guarantee to the organization customer satisfaction, continuous improvement and organizational effectiveness in order to achieve ma_imum competitiveness.
prepare weekly and monthly quality reports, make continuous quality improvement through good team work
connect customer needs with the conditions of the production process and define product guidelines and criteria and the conditions of the manufacturing process.
quality management system implement, monitor and maintain. conduct regular internal quality audits to ensure its effectiveness and suitability.
ensure that the quality management system (qms) is effectively established, implemented and maintained to be in compliance with iso9001, iso13485, 21 cfr 820, ce standards and chinese gmp.
manage all inspection instrument, inspection gages, and test fi_tures/tooling/equipment.
requirement:
10+ quality management e_perience,5+ site quality control e_perience in pharmaceutical, ivd or medical device industry
people management e_perience
e_perienced in iso 13485, 21 cfr 820,gmp,qsr
fda inspection e_perience
sound knowledge in process quality control and risk management
strong in leadership
good at communication, coordination
fluent in english
responsibilities:
in charge site quality control, quality system management.
set up the company quality goal and regularly review the status of quality target. train and guide the team to reach functional quality goal.
manage engineers and inspectors team of qa section, coordinate with other dept./team.
define the quality assurance policy and process, lead the implementation of quality assurance models and system that can guarantee to the organization customer satisfaction, continuous improvement and organizational effectiveness in order to achieve ma_imum competitiveness.
prepare weekly and monthly quality reports, make continuous quality improvement through good team work
connect customer needs with the conditions of the production process and define product guidelines and criteria and the conditions of the manufacturing process.
quality management system implement, monitor and maintain. conduct regular internal quality audits to ensure its effectiveness and suitability.
ensure that the quality management system (qms) is effectively established, implemented and maintained to be in compliance with iso9001, iso13485, 21 cfr 820, ce standards and chinese gmp.
manage all inspection instrument, inspection gages, and test fi_tures/tooling/equipment.
requirement:
10+ quality management e_perience,5+ site quality control e_perience in pharmaceutical, ivd or medical device industry
people management e_perience
e_perienced in iso 13485, 21 cfr 820,gmp,qsr
fda inspection e_perience
sound knowledge in process quality control and risk management
strong in leadership
good at communication, coordination
fluent in english
