歡迎光臨管理者范文網(wǎng)
當(dāng)前位置:管理者范文網(wǎng) > 安全管理 > 崗位職責(zé) > 崗位職責(zé)范文

基因檢測崗位職責(zé)匯編(6篇)

更新時間:2024-05-19 查看人數(shù):12

基因檢測崗位職責(zé)

崗位職責(zé)是什么

基因檢測崗位,是生物科學(xué)領(lǐng)域的一個關(guān)鍵職位,主要負(fù)責(zé)利用現(xiàn)代分子生物學(xué)技術(shù)對個體的基因信息進(jìn)行分析和解讀,以揭示遺傳特征、疾病風(fēng)險、藥物反應(yīng)性等重要信息。這個崗位的工作涵蓋了樣本處理、實(shí)驗(yàn)操作、數(shù)據(jù)分析等多個環(huán)節(jié),旨在為臨床診斷、個性化醫(yī)療、遺傳咨詢等領(lǐng)域提供科學(xué)依據(jù)。

崗位職責(zé)要求

1. 擁有生物學(xué)、遺傳學(xué)或相關(guān)領(lǐng)域的碩士及以上學(xué)歷,具備扎實(shí)的分子生物學(xué)基礎(chǔ)。

2. 熟練掌握基因測序技術(shù),如pcr、ngs(下一代測序)等,并能獨(dú)立進(jìn)行實(shí)驗(yàn)操作。

3. 具備數(shù)據(jù)分析能力,熟悉生物信息學(xué)工具和軟件,能對基因序列數(shù)據(jù)進(jìn)行解析和解讀。

4. 對遺傳學(xué)、醫(yī)學(xué)有深入理解,能將基因檢測結(jié)果與臨床表型關(guān)聯(lián)起來。

5. 注重細(xì)節(jié),具備嚴(yán)謹(jǐn)?shù)目蒲袘B(tài)度,確保實(shí)驗(yàn)數(shù)據(jù)的準(zhǔn)確性和可靠性。

6. 良好的團(tuán)隊(duì)協(xié)作精神,能夠與其他科學(xué)家、醫(yī)生、技術(shù)人員有效溝通。

7. 有生物醫(yī)學(xué)研究背景或臨床應(yīng)用經(jīng)驗(yàn)者優(yōu)先。

崗位職責(zé)描述

基因檢測崗位的日常工作包括:

1. 樣本管理:接收和處理各種生物樣本,確保樣本的質(zhì)量和安全性。

2. 實(shí)驗(yàn)操作:執(zhí)行基因提取、pcr擴(kuò)增、測序等實(shí)驗(yàn)步驟,記錄實(shí)驗(yàn)數(shù)據(jù)。

3. 數(shù)據(jù)分析:運(yùn)用生物信息學(xué)方法對測序數(shù)據(jù)進(jìn)行質(zhì)量控制、比對、變異檢測等分析。

4. 結(jié)果解讀:根據(jù)分析結(jié)果,撰寫報告,解釋基因變異對健康的影響,為臨床決策提供參考。

5. 技術(shù)研發(fā):參與新檢測方法和技術(shù)的研發(fā),提高檢測效率和準(zhǔn)確性。

6. 協(xié)作與溝通:與臨床醫(yī)生、研究人員討論病例,共同解決遺傳問題;與生物信息學(xué)家合作優(yōu)化分析流程。

有哪些內(nèi)容

基因檢測崗位涉及的內(nèi)容廣泛,包括但不限于:

1. 常見遺傳疾病的基因篩查,如癌癥、遺傳性疾病等。

2. 藥物代謝基因型檢測,以指導(dǎo)個體化用藥。

3. 遺傳咨詢,為患者和家屬解釋基因檢測結(jié)果,解答遺傳風(fēng)險相關(guān)疑問。

4. 基因組學(xué)研究,參與疾病機(jī)制、藥物靶點(diǎn)等基礎(chǔ)科研項(xiàng)目。

5. 新技術(shù)探索,如crispr-cas9基因編輯技術(shù)的應(yīng)用研究。

6. 倫理法規(guī)遵守,確?;驒z測工作的合規(guī)性,尊重個人隱私。

在這個崗位上,工作者需要不斷跟蹤生物科學(xué)和醫(yī)學(xué)的最新進(jìn)展,以適應(yīng)快速發(fā)展的基因檢測領(lǐng)域,為提高人類健康水平貢獻(xiàn)力量。

基因檢測崗位職責(zé)范文

第1篇 基因檢測銷售主管崗位職責(zé)

基因檢測銷售代表/銷售主管(北京) 維鵬云進(jìn) 上海維鵬云進(jìn)醫(yī)藥科技有限公司,維鵬云進(jìn),維鵬云進(jìn) 職位描述:

1、負(fù)責(zé)區(qū)域市場分子診斷產(chǎn)品的臨床開發(fā),完成銷售目標(biāo);

2、執(zhí)行公司制定的各類市場銷售活動方案,及時反饋市場信息,確保執(zhí)行效果;

3、客戶關(guān)系的維護(hù)及管理;

4、完成日常工作報表

職位要求:

1、大?;蛞陨蠈W(xué)歷,生物、醫(yī)學(xué)、市場營銷或相關(guān)專業(yè)背景;

2、一年以上基因檢測、醫(yī)學(xué)檢驗(yàn)項(xiàng)目、分子診斷產(chǎn)品、醫(yī)藥、醫(yī)療器械銷售工作經(jīng)驗(yàn),熟悉普外科或病理科客戶優(yōu)先;

3、具備獨(dú)立的市場開拓能力;

4、誠信務(wù)實(shí),有責(zé)任心,具有良好的人際溝通能力和團(tuán)隊(duì)合作精神;

第2篇 基因檢測技術(shù)員崗位職責(zé)

medical technologist-genomics 基因檢測技術(shù)員 科文斯醫(yī)藥研發(fā) 科文斯醫(yī)藥研發(fā)(北京)有限公司上海分公司,科文斯醫(yī)藥研發(fā),科文斯 responsibilities / duties:

? perform assigned clinical laboratory testing accurately and in a timely manner.

o resolve pendings. retrieve and check specimens against pending list. document specimen discrepancies. notify laboratory management when specimen discrepancies are not resolved.

o prepare workstation and instrumentation for the assigned testing. o properly handle specimens and independently resolve technical specimen issues in preparation for analysis and specimen storage. contact internal customers for clarification as needed.

o operate instruments to perform testing in accordance with established written procedures.

o performs routine testing and calculations as required.

o resolve routine and non-routine assay problems.

? ensure the validity of tests results through the performance of established quality assurance and quality control procedures.

o perform e_periments, as scheduled, for evaluation of new calibrator and/or qc lots. summarize results of investigations and compile data for review by management.

o document quality control results. interpret quality control results according to westgard rules or other established departmental procedures and accurately document biases, warnings and violations of control values.

o document corrective action for unusual occurrences (e.g. qc violations, instrument related problems).

o analyze proficiency testing survey samples as patient specimens. ? reagents/materials/supplies:

o receive, open and place in service all reagents/materials according to sops.

o prepare and properly label reagent, quality control, calibrator material.

o document implementation of new reagents/materials according to sops.

o perform parallel testing, linearity’s, stability, other quality control practices needed to ensure validity of material prior to being placed into service.

o perform inventory control of supplies and reagents as approved by management.

? result entry (auto-verification and manual entry).

o when data is manually entered (e.g. qc, patient data) ensure peer review is performed and documented prior to release of results.

o prepare proper documentation of test results and enter into the information system.

o generate an appropriate audit trail for all activities.

o document and communicate any result reporting problems or inconsistencies to laboratory management.

o complete testing within the e_pected turnaround time to meet customers’ e_pectations.

? ensures maintenance of instruments and equipment is performed according to manufacturer and sop requirements, and documented according to sop. o calibrate instruments, equipment and/or assays as required and document.

o perform basic instrument and equipment troubleshooting.

o perform pipette calibrations and document according to sop.

o notify laboratory management when an instrument or equipment does not meet specifications.

? comply with regulatory guidelines and covance standard operating procedures (sops) at all times.

? training

o individual is responsible for maintaining his/her complete up-to-date training file and is accountable for correcting and deficiencies found in his/her training file.

o individual is responsible for ensuring he/she is trained and training is documented prior to performing a task.

o the individual successfully completes, as scheduled, competency assessment and ensures competency testing documentation is provided to management for review/retention.

o competently performs department duties as set forth in the department training checklist(s).

o may assist in training new employees and follows-up to ensure training is understood.

o attends, as scheduled, department, mandatory and other meetings and training, as required according to training matrices.

? work to achieve partnership with both internal customers and e_ternal clients by:

o pull data in a timely manner for review by qa and e_ternal clients.

o contribute to the provision of accurate verbal or written response to internal qa and client audit findings. coordinate, where needed, with other resources to resolve issue.

o researches and prepares a response following investigation for quality purposes. coordinate, where needed, with other resources to resolve issue.

o research and responds in a timely manner to internal customer inquiries regarding status of test results, retrieval of samples for testing/storage and other needs.

o understand department metrics and goals.

? demonstrate proficiency in applicable computer systems and software.

? adheres to established safety policies and universal precaution guidelines at all times. maintains a clean, organized and safe work environment. minimizes biohazard waste. cleans workstation and materials daily.

? takes action for the department when additional responsibilities and opportunities are presented.

? provide laboratory management with a report of activities upon request.

? other duties as assigned.

education / qualifications

required:

? individual must qualify as testing personnel under moh regulations.

preferred:

? bachelors degree in medical technology or completion of at least a 12-month training program in medical technology.

or

? bachelors degree in a chemical, physical or biological science from an accredited college or university and one year training and/or e_perience in the specialty in which testing is to be performed. such training must be equivalent to that received in a school of medical technology.

e_perience

1 year lab e_perience, chemistry department prefer.

第3篇 基因檢測崗位職責(zé)

實(shí)驗(yàn)室pcr主管 北京京蒙高科干細(xì)胞技術(shù)有限公司細(xì)胞與分子臨床檢驗(yàn)所 北京京蒙高科干細(xì)胞技術(shù)有限公司細(xì)胞與分子臨床檢驗(yàn)所,京蒙干細(xì)胞細(xì)胞與分子臨床檢驗(yàn)所,京蒙 職責(zé)描述:

1、 熟悉pcr、凝膠電泳等一些基本分子生物學(xué)實(shí)驗(yàn)技能,熟悉分子生物學(xué)軟件分析;

2、 本實(shí)驗(yàn)室各組各項(xiàng)記錄的匯總和審查;

3、 負(fù)責(zé)實(shí)驗(yàn)室質(zhì)控和室間質(zhì)評的開展;

4、 安排并完成常規(guī)的基因檢測任務(wù)提供專業(yè)組內(nèi)目前行業(yè)內(nèi)先進(jìn)技術(shù)及新項(xiàng)目信息;

5、 熟練使用各種常用辦公軟件(word,e_cel,ppt);

6、 選拔優(yōu)秀人才作為本專業(yè)組的技術(shù)和管理骨干,做好梯隊(duì)建設(shè);

7、 完成上級布置的其他任務(wù)。

任職要求:

1、生物技術(shù)、生物工程、醫(yī)學(xué)等相關(guān)專業(yè);

2、從事相關(guān)工作三年以上,有特別豐富的相關(guān)工作經(jīng)驗(yàn)優(yōu)先;

3、熟悉分子診斷檢驗(yàn)技術(shù)(pcr或測序)、熟悉分子診斷產(chǎn)品、有檢驗(yàn)師資格證和有特檢檢測相關(guān)工作經(jīng)驗(yàn)優(yōu)先。

第4篇 基因檢測銷售經(jīng)理崗位職責(zé)

銷售經(jīng)理(基因檢測) 中玉金 中玉金標(biāo)記(北京)生物技術(shù)股份有限公司,中玉金,中玉金標(biāo)記,中玉金標(biāo)記 崗位職責(zé):

1、積極開拓區(qū)域內(nèi)第三方醫(yī)學(xué)檢驗(yàn)所及體檢機(jī)構(gòu)市場,達(dá)成市場占有率,完成銷售任務(wù);

2、掌握和創(chuàng)造客戶需求,主動為客戶提供周到細(xì)致服務(wù),完成項(xiàng)目合同簽訂;

3、分析市場構(gòu)成,進(jìn)行市場細(xì)分,調(diào)查行業(yè)產(chǎn)品情況,跟蹤市場動態(tài)變化,制定并完成市場推廣活動;

4、跟進(jìn)項(xiàng)目進(jìn)展,與各部門配合推動項(xiàng)目順利完成,按時完成回款,完成項(xiàng)目總結(jié);

5、完成出差、周度、月度、專項(xiàng)報告,配合完成各部門工作,完成其它安排的工作。

任職要求:

1、醫(yī)學(xué)、生物、檢驗(yàn)等相關(guān)專業(yè)大專及以上學(xué)歷;

2、2年以上醫(yī)療行業(yè)銷售經(jīng)驗(yàn),熟悉精準(zhǔn)醫(yī)療、醫(yī)學(xué)檢驗(yàn)市場;

3、熟悉分子生物、遺傳、醫(yī)學(xué)檢驗(yàn)相關(guān)業(yè)務(wù)領(lǐng)域?qū)I(yè)知識;

4、工作積極主動靈活,挑戰(zhàn),善于溝通和表達(dá),結(jié)果導(dǎo)向,計(jì)劃性強(qiáng)。

5、適應(yīng)長期出差。

金基因由中玉金標(biāo)記(北京)生物技術(shù)股份有限公司在____年初注冊成立,金基因標(biāo)志著中玉金標(biāo)記依托其龐大的硬件檢測平臺及核心科研團(tuán)隊(duì),為基因檢測領(lǐng)域提供可靠的、開放的第三方檢測平臺。

第5篇 基因檢測銷售代表崗位職責(zé)

基因檢測銷售代表/銷售主管(北京) 維鵬云進(jìn) 上海維鵬云進(jìn)醫(yī)藥科技有限公司,維鵬云進(jìn),維鵬云進(jìn) 職位描述:

1、負(fù)責(zé)區(qū)域市場分子診斷產(chǎn)品的臨床開發(fā),完成銷售目標(biāo);

2、執(zhí)行公司制定的各類市場銷售活動方案,及時反饋市場信息,確保執(zhí)行效果;

3、客戶關(guān)系的維護(hù)及管理;

4、完成日常工作報表

職位要求:

1、大?;蛞陨蠈W(xué)歷,生物、醫(yī)學(xué)、市場營銷或相關(guān)專業(yè)背景;

2、一年以上基因檢測、醫(yī)學(xué)檢驗(yàn)項(xiàng)目、分子診斷產(chǎn)品、醫(yī)藥、醫(yī)療器械銷售工作經(jīng)驗(yàn),熟悉普外科或病理科客戶優(yōu)先;

3、具備獨(dú)立的市場開拓能力;

4、誠信務(wù)實(shí),有責(zé)任心,具有良好的人際溝通能力和團(tuán)隊(duì)合作精神;

第6篇 基因檢測項(xiàng)目經(jīng)理崗位職責(zé)

1、負(fù)責(zé)基因產(chǎn)品的上線(包括產(chǎn)品市場調(diào)研、產(chǎn)品功能與用戶體驗(yàn)設(shè)計(jì),產(chǎn)品版本計(jì)劃等);

2、產(chǎn)品的包裝外觀及宣傳設(shè)計(jì);

3、負(fù)責(zé)產(chǎn)品優(yōu)化、維護(hù)與迭代;

4、負(fù)責(zé)行業(yè)動態(tài)收集整理與分析,參與用戶意見分析,為公司產(chǎn)品策略提供依據(jù)。

任職要求:

1、對基因測序行業(yè)和健康管理行業(yè)有一定了解,特別是針對個人基因市場有經(jīng)驗(yàn)的優(yōu)先。

2、有較強(qiáng)的項(xiàng)目管理與執(zhí)行能力;性格開朗,具有較強(qiáng)的表達(dá)能力、應(yīng)變能力和團(tuán)隊(duì)協(xié)作能力,能夠進(jìn)行良好的溝通。

4、本科以上學(xué)歷,基因、醫(yī)療或生物等相關(guān)專業(yè)。

5、有基因測序產(chǎn)品銷售(特別是大眾基因檢測市場銷售經(jīng)驗(yàn)者優(yōu)先考慮)、市場開拓、技術(shù)支持的工作經(jīng)驗(yàn)

基因檢測崗位職責(zé)匯編(6篇)

崗位職責(zé)是什么基因檢測崗位,是生物科學(xué)領(lǐng)域的一個關(guān)鍵職位,主要負(fù)責(zé)利用現(xiàn)代分子生物學(xué)技術(shù)對個體的基因信息進(jìn)行分析和解讀,以揭示遺傳特征、疾病風(fēng)險、藥物反應(yīng)性等重要信息
推薦度:
點(diǎn)擊下載文檔文檔為doc格式

相關(guān)基因檢測信息

  • 基因檢測崗位職責(zé)12篇
  • 基因檢測崗位職責(zé)12篇83人關(guān)注

    崗位職責(zé)是什么基因檢測崗位,是生物科學(xué)領(lǐng)域的一個關(guān)鍵職位,主要負(fù)責(zé)利用現(xiàn)代分子生物學(xué)技術(shù)對個體的基因信息進(jìn)行分析和解讀,以揭示遺傳特征、疾病風(fēng)險、藥物反應(yīng)性 ...[更多]

  • 基因檢測崗位職責(zé)匯編(6篇)
  • 基因檢測崗位職責(zé)匯編(6篇)12人關(guān)注

    崗位職責(zé)是什么基因檢測崗位,是生物科學(xué)領(lǐng)域的一個關(guān)鍵職位,主要負(fù)責(zé)利用現(xiàn)代分子生物學(xué)技術(shù)對個體的基因信息進(jìn)行分析和解讀,以揭示遺傳特征、疾病風(fēng)險、藥物反應(yīng)性 ...[更多]

崗位職責(zé)范文熱門信息