- 目錄
崗位職責(zé)是什么
檢測技術(shù)員是負(fù)責(zé)執(zhí)行各種檢測任務(wù)的專業(yè)人員，他們在生產(chǎn)流程、產(chǎn)品質(zhì)量控制和安全評估等領(lǐng)域發(fā)揮著至關(guān)重要的作用。他們運用專業(yè)的知識和技術(shù)手段，確保產(chǎn)品或服務(wù)符合既定的標(biāo)準(zhǔn)和規(guī)范。
崗位職責(zé)要求
1. 熟練掌握各類檢測設(shè)備的操作和維護(hù)，能夠準(zhǔn)確、高效地進(jìn)行檢測工作。
2. 具備扎實的科學(xué)基礎(chǔ)知識，特別是與檢測領(lǐng)域相關(guān)的物理、化學(xué)等專業(yè)知識。
3. 具有良好的問題解決能力，能迅速分析并解決檢測過程中遇到的問題。
4. 遵守實驗室安全規(guī)定，確保自身和他人的安全。
5. 保持高度的專業(yè)素養(yǎng)和責(zé)任感，確保檢測結(jié)果的公正、客觀和可靠。
崗位職責(zé)描述
檢測技術(shù)員的工作日常包括但不限于：
1. 執(zhí)行常規(guī)和復(fù)雜的檢測程序，如物理性能測試、化學(xué)成分分析等。
2. 記錄和分析檢測數(shù)據(jù)，編寫詳細(xì)的檢測報告，為生產(chǎn)和質(zhì)量改進(jìn)提供依據(jù)。
3. 參與新檢測方法的研發(fā)和現(xiàn)有方法的優(yōu)化，提高檢測效率和準(zhǔn)確性。
4. 對設(shè)備進(jìn)行定期維護(hù)和校準(zhǔn)，確保其正常運行。
5. 協(xié)助質(zhì)量管理部門處理不合格產(chǎn)品的調(diào)查和改進(jìn)措施的制定。
6. 參與內(nèi)部和外部的質(zhì)量審核，確保檢測體系的合規(guī)性。
有哪些內(nèi)容
1. 實驗室操作：進(jìn)行樣品采集、制備和實驗操作，如化學(xué)反應(yīng)、光學(xué)分析、機(jī)械性能測試等。
2. 數(shù)據(jù)管理：管理和整理檢測數(shù)據(jù)，確保數(shù)據(jù)的完整性和可追溯性。
3. 技術(shù)支持：為生產(chǎn)部門提供技術(shù)支持，解答關(guān)于檢測標(biāo)準(zhǔn)和方法的疑問。
4. 培訓(xùn)與指導(dǎo)：對新員工進(jìn)行檢測技能的培訓(xùn)和指導(dǎo)，提升團(tuán)隊整體技術(shù)水平。
5. 標(biāo)準(zhǔn)更新：關(guān)注行業(yè)動態(tài)，及時了解和應(yīng)用新的檢測標(biāo)準(zhǔn)和技術(shù)規(guī)范。
6. 客戶溝通：與客戶保持良好溝通，理解他們的需求，提供專業(yè)的檢測建議和服務(wù)。
檢測技術(shù)員的角色是保障產(chǎn)品質(zhì)量和企業(yè)信譽(yù)的關(guān)鍵，他們通過精準(zhǔn)的檢測工作，為企業(yè)的產(chǎn)品質(zhì)量和安全性提供堅實的后盾。
檢測技術(shù)員崗位職責(zé)范文
第1篇 實驗室檢測技術(shù)員崗位職責(zé)實驗室檢測技術(shù)員職責(zé)任職要求
實驗室檢測技術(shù)員崗位職責(zé)
崗位職責(zé):
1. 從事熒光定量pcr、一代/二代測序等實驗基本操作及數(shù)據(jù)分析等工作;
2. 及時處理臨床和市場部反饋的信息;
3. 撰寫sop等文件和報告;
4. 按照實驗室的質(zhì)量控制要求，填寫相關(guān)記錄表單，維護(hù)實驗儀器，保持實驗技術(shù)平臺的正常運轉(zhuǎn)。
任職資格:
1、分子生物學(xué)、醫(yī)學(xué)檢驗相關(guān)專業(yè)本科及以上學(xué)歷;
2、具有分子檢測技術(shù)平臺(pcr、測序、fish等)經(jīng)驗者優(yōu)先考慮;
3、有檢驗師資格證者或pcr上崗證者優(yōu)先考慮;
4、誠實正直，工作認(rèn)真嚴(yán)謹(jǐn)，具有良好的團(tuán)隊合作精神，具有高度的責(zé)任感和敬業(yè)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 檢測技術(shù)員崗位職責(zé)
檢測技術(shù)員 深圳市卓爾悅電子科技有限公司 深圳市卓爾悅電子科技有限公司,卓爾悅 職責(zé)描述:1、負(fù)責(zé)環(huán)境可靠性設(shè)備的使用及維護(hù);
2、熟悉gb/t 2423系列標(biāo)準(zhǔn)和獨立按標(biāo)準(zhǔn)進(jìn)行測試,主要是高低溫、沖擊、振動、低氣壓、跌落等相關(guān)測試,并具有一定的電路知識;
3、負(fù)責(zé)試驗樣品的測試,審核測試數(shù)據(jù)的標(biāo)準(zhǔn)性及出具相應(yīng)的環(huán)境測試報告;
4、對cnas和cma體系有一定的了解,有良好的溝通能力和團(tuán)隊協(xié)助精神,具有吃苦耐勞的精神
2004 5625-58|154 4582 2451 55
5、有第三方測試機(jī)構(gòu)測試經(jīng)驗優(yōu)先考慮。
第4篇 無損檢測技術(shù)員崗位職責(zé)
無損檢測技術(shù)員 中廣核檢測技術(shù)有限公司蘇州分公司 中廣核檢測技術(shù)有限公司蘇州分公司,中廣核 職責(zé)描述:
1.掌握本專業(yè)工作中相關(guān)知識與技能,參與本專業(yè)相關(guān)日常的本部準(zhǔn)備工作及現(xiàn)場檢驗活動。
2.參與本專業(yè)相關(guān)的設(shè)備管理、維護(hù)、維修、保養(yǎng)和調(diào)試等工作。
3.能夠圓滿完成上級領(lǐng)導(dǎo)安排的其他各項工作任務(wù)。
4.熟悉無損檢測專業(yè),如超聲,渦流,表面,射線等。
5.工作中積極主動,能快速較好的完成任務(wù),團(tuán)隊協(xié)助能力強(qiáng)。遵循標(biāo)準(zhǔn)工作流程,確保檢驗質(zhì)量。
6.適應(yīng)出差。
第5篇 消防檢測技術(shù)員崗位職責(zé)
1、熟悉大廈日常消防設(shè)備維保工作,對消防設(shè)施的故障進(jìn)行維修排除; 2、具有消防工程或消防維保工作經(jīng)驗一年以上;熟悉給排水系統(tǒng),能進(jìn)行水泵控制柜、風(fēng)機(jī)控制柜故障的判斷與維修; 3、有較強(qiáng)應(yīng)變能力,有責(zé)任心,良好的團(tuán)隊合作精神; 4、較強(qiáng)的溝通協(xié)調(diào)能力,善于處理客戶人際關(guān)系;有良好的客戶服務(wù)意識。
第6篇 環(huán)境檢測技術(shù)員崗位職責(zé)任職要求
環(huán)境檢測技術(shù)員崗位職責(zé)
崗位職責(zé):
1.按測試項目的要求開展測試，填寫相關(guān)測試記錄并出具完整的原始數(shù)據(jù);
2.保證樣品測試的時效性，按照公司質(zhì)量控制要求開展測試;
3.負(fù)責(zé)所屬實驗區(qū)域的5s整理，分析儀器的維護(hù)與管理;
4.負(fù)責(zé)所分配的新項目的研發(fā)與能力驗證考核樣品的測試;
5.定期總結(jié)檢測工作中遇到的異常情況及解決方案，向分析負(fù)責(zé)人匯報;
6.完成領(lǐng)導(dǎo)安排的其他工作。
任職條件:
1、大專及以上學(xué)歷，環(huán)境或化學(xué)、生物、食品等相關(guān)專業(yè);
2、有相關(guān)從業(yè)經(jīng)驗優(yōu)先;
3、熟練操作化學(xué)分析用儀器設(shè)備;
4、勤奮好學(xué)、溝通表達(dá)能力良好，能吃苦耐勞。
5、也非常歡迎應(yīng)屆生的加入。
環(huán)境檢測技術(shù)員崗位
第7篇 基因檢測技術(shù)員崗位職責(zé)基因檢測技術(shù)員職責(zé)任職要求
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 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8篇 無損檢測技術(shù)員崗位職責(zé)任職要求
無損檢測技術(shù)員崗位職責(zé)
職責(zé)描述:
對2019年新改擴(kuò)建500kv及以上變電工程gis殼體接焊縫進(jìn)行監(jiān)督檢測，對地腳螺栓和螺母進(jìn)行型式尺寸及標(biāo)識檢測并出具報告，2，協(xié)助對金屬技術(shù)監(jiān)督工作情況和檢測質(zhì)量進(jìn)行監(jiān)督檢查及現(xiàn)場復(fù)核
任職要求:持有中國質(zhì)量監(jiān)督局特種設(shè)備ut.rt二級證書(及以上)，3-5年相關(guān)工作經(jīng)驗 ; 熟悉4730標(biāo)準(zhǔn) 有鋁合金檢測經(jīng)驗優(yōu)先
無損檢測技術(shù)員崗位
第9篇 實驗室檢測技術(shù)員崗位職責(zé)
company profile:
our gtc lab in shanghai offers e_tended reliable testing services on component materials or finished products to verify levels of the restricted substances and develops sound, sensible analytical methods with international standards, such as european regulations.
various spectroscopy and wet chemistry methods are used to determine the concentrations of restricted substances in mechanical components, environmental samples, food or pharmaceuticals.
all testing results from our lab are fully documented in certified test reports for our customers’records.
job description:
1. be responsible for testing of products & materials
2. be responsible for operation and maintenance of gc-ms, lc-ms, _rf, icp-oes, icp-ms, uv-vis, etc.
3. other lab daily work, including quality control and related record
4. support supervisor to trace testing status
job requirement:
1. junior college degree or above, major in chemistry, ideally analytical chemistry;
2. have 2-year or above working e_perience in material testing; be familiar with eu and china rohs regulatory requirements and reach, weee etc.; understanding the food contact material regulation of different countries is an advantage
3. have operation e_perience of common analytical instruments, such as gc-ms, lc-ms, _rf, icp-oes, icp-ms, uv-vis, etc
4. good command of english
5. good communication skills
6. hardworking, self-motivated, fast-learning and teamwork spirits
第10篇 環(huán)境檢測技術(shù)員崗位職責(zé)
根據(jù)公司發(fā)展戰(zhàn)略與業(yè)務(wù)和國家環(huán)境保護(hù)需要,具體負(fù)責(zé)環(huán)保車間日常排放工業(yè)廢水檢驗監(jiān)測等工作,確保工業(yè)廢水達(dá)到國家排放標(biāo)準(zhǔn)標(biāo)要求,為廢水處理和生產(chǎn)廠的正常生產(chǎn)提供保障。
1、建立健全環(huán)境監(jiān)測管理制度和工業(yè)廢水檢測作業(yè)指導(dǎo)書,并及時進(jìn)行優(yōu)化調(diào)整;
2、建立環(huán)境監(jiān)測設(shè)備臺帳,負(fù)責(zé)檢測設(shè)備日常的維護(hù)工作;
3、建立監(jiān)測數(shù)據(jù)表格、及時填寫和上報,并負(fù)責(zé)歸檔保存;
4、負(fù)責(zé)日常監(jiān)測數(shù)據(jù)向環(huán)保車間反饋,及時溝通監(jiān)測結(jié)果;
5、參與“三廢”處理過程問題分析和持續(xù)改進(jìn);
6、執(zhí)行崗位安全生產(chǎn)責(zé)任制;
7、完成公司和部門安排的其他工作任務(wù)。
第11篇 消防檢測技術(shù)員崗位職責(zé)任職要求
消防檢測技術(shù)員崗位職責(zé)
崗位職責(zé):
1、在消防主檢帶領(lǐng)下進(jìn)行檢測工作，嚴(yán)格遵守相關(guān)技術(shù)標(biāo)準(zhǔn)操作規(guī)程，按時完成工作任務(wù);
2、愛護(hù)檢測儀器設(shè)備，能夠熟練操作使用儀器設(shè)備，并懂得儀器設(shè)備的日常維護(hù)、保養(yǎng)工作;
3、認(rèn)真及時做好檢測的原始記錄及儀器的運行記錄，確保檢測工作的正確、完整、清晰;
4、檢測過程中發(fā)現(xiàn)異常情況及時向部門負(fù)責(zé)人匯報;
5、負(fù)責(zé)協(xié)助主檢進(jìn)行消防工程竣工檢測，建筑物年度檢測工作。
6、工作認(rèn)真、敬業(yè)，責(zé)任心強(qiáng)，具有良好的團(tuán)隊意識和合作精神;
7、身體健康，無不良嗜好
任職資格:
1、機(jī)電一體化，電氣工程及自動化專業(yè)等相關(guān)專業(yè)大專以上學(xué)歷，從事過消防安裝維修工作一年以上，熟悉消防系統(tǒng);
2、掌握消防系統(tǒng)的工作原理、組成結(jié)構(gòu)、檢測方法、故障特點、排除技術(shù)、保養(yǎng)規(guī)范;
3、持有消防操作員證和電工證者優(yōu)先;
4、有團(tuán)隊精神，服從安排，具備較好的溝通能力。
消防檢測技術(shù)員崗位
第12篇 檢測技術(shù)員崗位職責(zé)任職要求
檢測技術(shù)員崗位職責(zé)
檢測技術(shù)員 麗華(廣州)香精香料股份有限公司 麗華(廣州)香精香料股份有限公司，麗華職位要求:
1、大專以上，精細(xì)化工或食品等相關(guān)專業(yè)，具有食品檢驗工等相關(guān)資質(zhì)
2、1年以上工廠檢驗部門或第三方檢測機(jī)構(gòu)實驗室工作經(jīng)驗
3、易于溝通，積極進(jìn)取;
工作職責(zé):
1、原材料品質(zhì)檢驗
2、 產(chǎn)品品質(zhì)檢驗
3、實驗室維護(hù)管理
檢測技術(shù)員崗位
第13篇 材料檢測技術(shù)員崗位職責(zé)描述崗位要求
職位描述：
崗位職責(zé)：
1、負(fù)責(zé)精密鑄造葉片、蠟?zāi)?、陶芯等尺寸檢測；
2、獨立操作顯微鏡、超聲波測厚儀等檢測設(shè)備的操作，負(fù)責(zé)三坐標(biāo)、藍(lán)光尺寸檢查，超聲壁厚檢測；
3、進(jìn)行金相、晶粒取向、晶粒度等目視檢查。
崗位要求：
1、全日制本科及以上學(xué)歷，檢測類、材料類、冶金類等相關(guān)專業(yè)；
2、具有材料檢測相關(guān)工作經(jīng)驗，優(yōu)秀應(yīng)屆畢業(yè)生可考慮；
3、工作積極主動， 態(tài)度認(rèn)真，踏實肯干。
集團(tuán)上市公司的平臺，廣闊的發(fā)展前景，國際一流水平的研發(fā)技術(shù)和團(tuán)隊！
