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職位描述：

年齡:最好52歲以下，做事踏實(shí)服從安排比較優(yōu)秀的可以放寬到55以下，會(huì)開電動(dòng)叉車的優(yōu)先考慮。
工作時(shí)間:
早上八點(diǎn)半上班，下午四點(diǎn)半下班。
工作內(nèi)容:
搬運(yùn)和清潔等體力勞動(dòng)。
文化:初中以上，會(huì)認(rèn)字寫字，涉及簡單的填寫記錄要會(huì)簽名。
健康:
①因?yàn)闀?huì)直接接觸生產(chǎn)原輔料和藥品，不能攜帶傳染性疾病，如乙肝丙肝艾滋梅毒。
②無心臟疾病。
③無嚴(yán)重的腰椎疾病。

職位描述：

1.英語6級(jí)以上 2.吃苦耐勞，有合作精神 3.最好有植提相關(guān)經(jīng)驗(yàn)

職位描述：

崗位職責(zé)： 1、 熟悉細(xì)胞培養(yǎng)、測定細(xì)胞生長類實(shí)驗(yàn)（CCK-8、MTT、細(xì)胞凋亡）、Western Blot、PCR、動(dòng)物疾病模型（如小鼠移植瘤模型、小鼠耳腫脹模型或肺血栓小鼠模型等）、制作組織切片或免疫組化中一種或幾種實(shí)驗(yàn)操作。 2、熟悉熒光顯微鏡、PCR儀、酶標(biāo)儀、組織切片機(jī)、凝膠成像系統(tǒng)、化學(xué)發(fā)光成像系統(tǒng)或流式細(xì)胞儀一種設(shè)備或多種設(shè)備 3、能夠根據(jù)實(shí)驗(yàn)方案進(jìn)行實(shí)驗(yàn)操作，并能依照實(shí)驗(yàn)具體情況調(diào)整實(shí)驗(yàn)方案； 4、完成上級(jí)交代的其他任務(wù)； 任職要求： 1、生命科學(xué)、生物工程、藥學(xué)、分子生物學(xué)、細(xì)胞生物學(xué)、動(dòng)物科學(xué)或醫(yī)學(xué)等相關(guān)專業(yè)大專以上學(xué)歷； 2、具有較強(qiáng)的溝通能力與分析能力，良好的團(tuán)隊(duì)合作能力； 3、有較強(qiáng)的責(zé)任心和事業(yè)心，認(rèn)真負(fù)責(zé)；

職位描述：

藥企車間可坐可站，輕松不累，長白班

職位描述：

Why KOL/ HCP/ Patients Need You

Field-based medical colleagues provide therapeutic area /product expertise to health care providers. You will think big and demonstrate every day that we're a patient-centric company by looking to improve health outcomes for patients.

Maximize the value of Pfizer products to Chinese patients and health care professional through medical activities in assigned territory. Implement medical/research/disease management programs; introduce new concept through medical education to help doctors to improve patients’ outcome; conduct medical to medical communication to transport product knowledge and therapeutic update to key influencers and stakeholders; and provide professional medical training to commercial teams.

Lead medical to medical communication

• Lead and develop regional level medical strategy in the designed therapeutic area
• KOL mapping in responsible region and conduct regular medical communication face to face and virtually.
• Organize regional level medical to medical meeting and activities with KOLs to deliver cutting edge medical information of defined therapeutic area and assigned products
• Conduct medical educational meeting to introduce new concept to help doctors to improve patients’ outcome and advance their research capability
• Speak at medical communication meeting at national and regional level.
• Provide timely feedback of KOL’s comments and insights to supervisors and relevant medical advisors
• Respond medical inquiries as needed.
• Establish good academic relationship with regional academic origination at defined therapeutic area.
• Cooperate and align with medical advisors to engage KOLs

Medical input to product medical and brand plan

• Collect, analyze, and report timely local customer medical insights to input on product strategy and message development
• Work with (Senior) medical advisor and local marketing manager proactively to assist product strategy implementation

Implementation clinical research

• Support Pfizer sponsored Non interventional study at regional level.
• Support Non-Pfizer sponsored investigator-initiated product-related clinical research at regional level.
• Discuss research concept with interested researcher, and communicated the nature and requirement of Pfizer’s ISR based on ISR strategies
• Facilitate submission of investigator initiated pre-clinical and clinical proposals, and act as a Liaison between Pfizer and ISR researcher; and follow up ISR on its progress according to timeline

Implementation medical program and activities

• Develop KOL engagement related conference or program plan based on regional level medical strategy
• Implement conference or program according to timeline and with good quality.

Improve sale team medical ability through medical training, literature delivery and medical knowledge

• Organize face to face meeting or online meeting to cascade medical information to improve sale team’s medical ability
• Provide customized response for common medical queries in the field for assigned products.
• Present at POA and regional sales meetings for medical information

Collaborate with SMEs to jointly boost customer experience and satisfaction by enhanced scientific exchange, broader market coverage, faster responses

• Collaborate with commercial account SME, for medical solutions to HCP, via the internal strategic alignment
• Provide RWE related consultation and cooperation to HCP, with Medical RWE expert’s support
• Set up and facilitate Pre-launch medical work in the field, with Medical Pre-launch team’s guidance
• Facilitate the related work to ensure Patient centricity, with Medical Patient Engagement’s guidance

Ensure company’s medical compliance

• Implement medical programs and activities within medical compliance
• Communicate medical information with compliance
• Ensure timely SOP learning, and daily practice compliant with SOPs.
• Ensure collaboration with commercial colleagues within medical compliance

• Technical
• Therapeutic area knowledge: background with the disease knowledge and clinical practice of the therapeutic area
• Language: Proficiency in oral and written English
• Software: Good at Microsoft Office software
• Strong business acumen
• Cross functional leadership skill
• Strong communication and influencing skill
• Managerial
• Sustain Focus on Performance
• Create an Inclusive Environment
• Encourage Open Discussion and Debate
• Manage Change
• Develop People
• Align Across Pfizer
• Education
• Medical or Biopharmaceutical related Background, Public health related background for vaccine, Master Degree or above, Ph D or MD in the defined therapeutic area is preferred.

• About 2 years clinical practice or medical affairs experience in other multinational pharmaceutical companies
• Good medical knowledge in the defined therapeutic area
• Good understanding about pharmaceutical business
• Abundant clinical studies experience in multinational pharmaceutical companies

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

職位描述：

崗位要求： 1、 醫(yī)藥、化學(xué)、化工、生物工程、制藥類等相關(guān)專業(yè)； 2、 本科及以上學(xué)歷，優(yōu)秀應(yīng)屆生，可接受實(shí)習(xí)； 培養(yǎng)方向：質(zhì)量管理-質(zhì)量經(jīng)理 崗位職責(zé)： 1、本崗位質(zhì)量管理分三塊工作內(nèi)容，質(zhì)量體系文件的管理，現(xiàn)場QA及供應(yīng)商管理； 2、質(zhì)量體系文件管理：管理受控文件和記錄，確保文件和記錄的修訂，發(fā)放，存檔，收回和銷毀符合程序規(guī)定； 在原輔料、半成品、成品放行前對批記錄和檢驗(yàn)記錄進(jìn)行審核，確保產(chǎn)品生產(chǎn)符合既定標(biāo)準(zhǔn)；組織實(shí)施公司內(nèi)審工作，制定年度內(nèi)審計(jì)劃、審查記錄，編制內(nèi)審報(bào)告等；負(fù)責(zé)客戶來司審計(jì)工作。 3、現(xiàn)場QA：負(fù)責(zé)生產(chǎn)過程中GMP相關(guān)工作的日常管理和監(jiān)督工作，統(tǒng)計(jì)分析生產(chǎn)監(jiān)督過程中存在問題、偏差/異常及工序控制數(shù)據(jù)分析，參與變更、偏差和調(diào)查；組織人員變更評估，跟蹤變更執(zhí)行，管理變更過程。 4、供應(yīng)商管理：參與主要物料供應(yīng)商審計(jì)，必要時(shí)對供應(yīng)商進(jìn)行現(xiàn)場審計(jì)；供應(yīng)商的開發(fā)/輔導(dǎo)/考核/評鑒系統(tǒng)的完善與實(shí)施。 薪酬福利： 1、雙休八小時(shí)工時(shí)制，入職繳納五險(xiǎn)一金； 2、試用期薪資3.5-4K左右，轉(zhuǎn)正后年薪5-8W； 3、尊重員工個(gè)人才能的發(fā)揮； 4、正常出勤提供中餐，提供住宿； 5、各節(jié)假日福利，保障員工后勤生活； 6、公司目前位于杭州市桐廬縣，將于2021年搬遷至衢州江山。

職位描述：

崗位要求： 1、藥學(xué)或制藥工程相關(guān)專業(yè)，本科學(xué)歷； 2、熟悉GMP，能編寫技術(shù)文件，有一到兩年藥廠生產(chǎn)工作經(jīng)驗(yàn)者優(yōu)先； 3、有凍干粉針劑生產(chǎn)經(jīng)歷者優(yōu)先 。

職位描述：

Why KOL/ HCP/ Patients Need You

Field-based medical colleagues provide therapeutic area /product expertise to health care providers. You will think big and demonstrate every day that we're a patient-centric company by looking to improve health outcomes for patients.

Maximize the value of Pfizer products to Chinese patients and health care professional through medical activities in assigned territory. Implement medical/research/disease management programs; introduce new concept through medical education to help doctors to improve patients’ outcome; conduct medical to medical communication to transport product knowledge and therapeutic update to key influencers and stakeholders; and provide professional medical training to commercial teams.

Lead medical to medical communication

• Lead and develop regional level medical strategy in the designed therapeutic area
• KOL mapping in responsible region and conduct regular medical communication face to face and virtually.
• Organize regional level medical to medical meeting and activities with KOLs to deliver cutting edge medical information of defined therapeutic area and assigned products
• Conduct medical educational meeting to introduce new concept to help doctors to improve patients’ outcome and advance their research capability
• Speak at medical communication meeting at national and regional level.
• Provide timely feedback of KOL’s comments and insights to supervisors and relevant medical advisors
• Respond medical inquiries as needed.
• Establish good academic relationship with regional academic origination at defined therapeutic area.
• Cooperate and align with medical advisors to engage KOLs

Medical input to product medical and brand plan

• Collect, analyze, and report timely local customer medical insights to input on product strategy and message development
• Work with (Senior) medical advisor and local marketing manager proactively to assist product strategy implementation

Implementation clinical research

• Support Pfizer sponsored Non interventional study at regional level.
• Support Non-Pfizer sponsored investigator-initiated product-related clinical research at regional level.
• Discuss research concept with interested researcher, and communicated the nature and requirement of Pfizer’s ISR based on ISR strategies
• Facilitate submission of investigator initiated pre-clinical and clinical proposals, and act as a Liaison between Pfizer and ISR researcher; and follow up ISR on its progress according to timeline

Implementation medical program and activities

• Develop KOL engagement related conference or program plan based on regional level medical strategy
• Implement conference or program according to timeline and with good quality.

Improve sale team medical ability through medical training, literature delivery and medical knowledge

• Organize face to face meeting or online meeting to cascade medical information to improve sale team’s medical ability
• Provide customized response for common medical queries in the field for assigned products.
• Present at POA and regional sales meetings for medical information

Collaborate with SMEs to jointly boost customer experience and satisfaction by enhanced scientific exchange, broader market coverage, faster responses

• Collaborate with commercial account SME, for medical solutions to HCP, via the internal strategic alignment
• Provide RWE related consultation and cooperation to HCP, with Medical RWE expert’s support
• Set up and facilitate Pre-launch medical work in the field, with Medical Pre-launch team’s guidance
• Facilitate the related work to ensure Patient centricity, with Medical Patient Engagement’s guidance

Ensure company’s medical compliance

• Implement medical programs and activities within medical compliance
• Communicate medical information with compliance
• Ensure timely SOP learning, and daily practice compliant with SOPs.
• Ensure collaboration with commercial colleagues within medical compliance

• Technical
• Therapeutic area knowledge: background with the disease knowledge and clinical practice of the therapeutic area
• Language: Proficiency in oral and written English
• Software: Good at Microsoft Office software
• Strong business acumen
• Cross functional leadership skill
• Strong communication and influencing skill
• Managerial
• Sustain Focus on Performance
• Create an Inclusive Environment
• Encourage Open Discussion and Debate
• Manage Change
• Develop People
• Align Across Pfizer
• Education
• Medical or Biopharmaceutical related Background, Public health related background for vaccine, Master Degree or above, Ph D or MD in the defined therapeutic area is preferred.

• About 2 years clinical practice or medical affairs experience in other multinational pharmaceutical companies
• Good medical knowledge in the defined therapeutic area
• Good understanding about pharmaceutical business
• Abundant clinical studies experience in multinational pharmaceutical companies

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

職位描述：

男女不限，20-35歲，中專及以上文憑，生物醫(yī)藥（倉管）工作經(jīng)驗(yàn)優(yōu)先 工作描述 1、能熟練使用辦公軟件； 2、工作認(rèn)真負(fù)責(zé)、細(xì)心，條理性強(qiáng)； 3、工作內(nèi)容：核對訂單，打包發(fā)貨等；

職位描述：

工作職責(zé)：
1.對大灣區(qū)生物制藥、醫(yī)療領(lǐng)域的展會(huì)進(jìn)行深入調(diào)研，分析整理行業(yè)競爭對手情況；
2.開拓大灣區(qū)的相關(guān)領(lǐng)域的協(xié)會(huì)、專業(yè)機(jī)構(gòu)，生物園區(qū)等，并建立合作關(guān)系；
3.尋找大灣區(qū)可能合作的展覽或是可收購的關(guān)聯(lián)展會(huì)；
4.對行業(yè)市場發(fā)展趨勢高度關(guān)注，尋找、挖掘新的合作資源，探索新業(yè)務(wù)的方向及思路；
5.開拓大灣區(qū)的生物制藥大客戶；
6.收集客戶資料，做好客戶的整理、篩選、跟進(jìn)工作；
7.完成項(xiàng)目開拓中的其它事項(xiàng)。
崗位要求：
1.本科以上學(xué)歷，市場營銷、工商管理等相關(guān)專業(yè)；
2.3年以上醫(yī)藥領(lǐng)域展覽會(huì)議、媒體廣告相關(guān)公司工作經(jīng)驗(yàn)；
3.有當(dāng)?shù)厣镏扑?、醫(yī)療領(lǐng)域客戶資源、相關(guān)行業(yè)協(xié)會(huì)、機(jī)構(gòu)及園區(qū)資源者優(yōu)先；
4.有較強(qiáng)的商務(wù)交際和開拓能力，能承受工作壓力，敢于挑戰(zhàn)；
5.具備較強(qiáng)的學(xué)習(xí)能力，善于人際溝通，樂觀開朗，心態(tài)積極。

職位描述：

車間操作工，男，25-45歲，有化工行業(yè)經(jīng)驗(yàn)者優(yōu)先。

職位描述：

1.負(fù)責(zé)建立監(jiān)督醫(yī)療器械GMP的有效執(zhí)行， 2.熟悉IS13485質(zhì)量體系， 3.負(fù)責(zé)醫(yī)療器械質(zhì)量文件的建立。

職位描述：

成都科銳動(dòng)物藥業(yè)崗位招聘 簡介：成都科銳動(dòng)物藥業(yè)有限公司，多年專業(yè)從事獸藥水針、粉針、中藥提取生產(chǎn)。 一、招聘崗位：QC檢驗(yàn)員2名。設(shè)備部經(jīng)理、機(jī)械維修2名。 二、QC檢驗(yàn)員崗位要求： 1、 產(chǎn)品檢測、分析化學(xué)、食品檢測、中醫(yī)藥相關(guān)專業(yè)，?？萍耙陨蠈W(xué)歷、從事醫(yī)藥相關(guān)檢 驗(yàn)工作3年以上。 2、 年齡要求：30-40歲，男女不限。 三、設(shè)備維修管理崗位要求： 1、機(jī)電專業(yè)相關(guān)專業(yè)、具有高中以上文化、從事食品醫(yī)藥設(shè)備維修工作3年以上。 1、 年齡要求：30-45歲，限男性。 二：薪資及福利待遇： 1、QC檢驗(yàn)員：月固定工作4500至6000＋績效工資＋五險(xiǎn)＋免費(fèi)提供住宿。 2、熟練工試用期1個(gè)月，與轉(zhuǎn)正后合同工資一樣。 三、設(shè)備維修部經(jīng)理： 1、設(shè)備維修部經(jīng)理、月固定工作5000至8000＋績效工資＋五險(xiǎn)＋免費(fèi)提供住宿。 2、機(jī)器維修：月固定工作4000至6000＋績效工資＋五險(xiǎn)＋免費(fèi)提供住宿。 3、熟練工試用期1個(gè)月，與轉(zhuǎn)正后合同工資一樣。 四、休假：周單休日、節(jié)假日參照國家規(guī)定執(zhí)行、也可調(diào)休。 工作地點(diǎn)：成都市新都區(qū)工業(yè)園區(qū)炬光路70號(hào)。 聯(lián) 系 人：李先生、 電話：13808059439 許先生、 電話：13880507996 發(fā)布時(shí)間：2021年5月30日

職位描述：

任職要求： 1、大專學(xué)歷，制藥相關(guān)專業(yè)； 2、中專有工作經(jīng)驗(yàn)的亦可； 工作內(nèi)容： 從事公司注射劑產(chǎn)品的生產(chǎn)工作

職位描述：

任職要求： 1、本科、碩士學(xué)歷； 2、臨床藥學(xué)、藥學(xué)、醫(yī)學(xué)相關(guān)專業(yè) 3、英語水平CET6；熟悉ICH GCP和國內(nèi)相關(guān)法規(guī) 主要工作內(nèi)容： 1、IND申報(bào)之前負(fù)責(zé)臨床CRO的調(diào)研，參與臨床CRO的評估和篩選，參與臨床研究計(jì)劃的撰寫，IND申報(bào)之后負(fù)責(zé)對第三方臨床工作的核查和協(xié)調(diào)。 2、臨床政策法規(guī)的跟進(jìn)和解讀。 3、公司仿制藥品種一致性評價(jià)的協(xié)調(diào)和對接，具體開展后的核查和協(xié)調(diào)。