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、實驗操作、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，并能獨立進(jìn)行實驗操作。
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，確保實驗數(shù)據(jù)的準(zhǔn)確性和可靠性。
6. 良好的團(tuán)隊協(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. 實驗操作：執(zhí)行基因提取、pcr擴(kuò)增、測序等實驗步驟，記錄實驗數(shù)據(jù)。
3. 數(shù)據(jù)分析：運用生物信息學(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、藥物靶點等基礎(chǔ)科研項目。
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、大專或以上學(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)檢驗項目、分子診斷產(chǎn)品、醫(yī)藥、醫(yī)療器械銷售工作經(jīng)驗,熟悉普外科或病理科客戶優(yōu)先;
3、具備獨立的市場開拓能力;
4、誠信務(wù)實,有責(zé)任心,具有良好的人際溝通能力和團(tuán)隊合作精神;
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)
實驗室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)胞與分子臨床檢驗所,京蒙干細(xì)胞細(xì)胞與分子臨床檢驗所,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)實驗技能,熟悉分子生物學(xué)軟件分析;
2、 本實驗室各組各項記錄的匯總和審查;
3、 負(fù)責(zé)實驗室質(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)驗優(yōu)先;
3、熟悉分子診斷檢驗技術(shù)(pcr或測序)、熟悉分子診斷產(chǎn)品、有檢驗師資格證和有特檢檢測相關(guān)工作經(jīng)驗優(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)項目進(jìn)展,與各部門配合推動項目順利完成,按時完成回款,完成項目總結(jié);
5、完成出差、周度、月度、專項報告,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,熟悉精準(zhǔn)醫(yī)療、醫(yī)學(xué)檢驗市場;
3、熟悉分子生物、遺傳、醫(yī)學(xué)檢驗相關(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,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)檢驗項目、分子診斷產(chǎn)品、醫(yī)藥、醫(yī)療器械銷售工作經(jīng)驗,熟悉普外科或病理科客戶優(yōu)先;
3、具備獨立的市場開拓能力;
4、誠信務(wù)實,有責(zé)任心,具有良好的人際溝通能力和團(tuán)隊合作精神;
第6篇 基因檢測項目經(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)品功能與用戶體驗設(shè)計,產(chǎn)品版本計劃等);
2、產(chǎn)品的包裝外觀及宣傳設(shè)計;
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)驗的優(yōu)先。
2、有較強(qiáng)的項目管理與執(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)驗者優(yōu)先考慮)、市場開拓、技術(shù)支持的工作經(jīng)驗
