科文斯医药研发（北京）有限公司上海分公司最新招聘信息

科文斯医药研发（北京）有限公司上海分公司最新招聘信息

公司简介

科文斯，全球性的合同研究组织（CRO）Covance Inc.是全球服务最全面的药物研发公司。 

我们致力于推动医疗保健事业发展并实现Solutions MadeReal®，通过向制药公司和生物科技公司提供高质量的非临床、临床前试验、临床和商业化服务，帮助减少药物研发的时间和成本。凭借丰富的经验与深厚知识，我们具备独特的优势，能为客户合作伙伴提供不仅仅局限于测试的独到见解。 

我们还向化学品、农用化学品和食品行业提供实验室测试服务，同时也是毒理学分析服务、中心实验室服务、药物筛选服务的市场领导者，以及III期临床试验管理服务的全球顶级提供商。

招聘岗位：实习生（2020届or2021届）                薪资面议               本科              应届生/实习生

职位描述：

该岗位2019年6月3日前在普陀区岚皋路品尊国际实习。6月3日后至浦东新区伽利略路338号亚兰德商业中心。 

工作内容: 
1.业务数据汇总录入、各类工作表格更新维护； 
2.协助费用请款、报销流程的跟进； 
3.日常行政类工作，文档、资料整理归档，会议支持等。 

任职要求： 
1.能够提供至少一周3天实习， 至少提供6个月实习； 
2.2020届大三在读，专业不限，医药，生物类专业优先； 
3.英语良好，读写无障碍； 

职位要求：

专业要求：药学,外国语言学

最低学历：本科

工作年限：在读学生

职称要求：不限

地址：上海浦东新区伽利略路338号9号楼（有班车）

招聘岗位：实验室报告审核员 QC Reviewer                  6k~12k/月               本科                  1~3年经验

职位描述：

Responsibilities / Duties: 
• Reviews data packets and forms for all study types. 
• Utilizes knowledge of Nautilus, Analyst, and Dial M software forreview of electronic data. 
• Responds to QA inspection report findings related to QC review ofdata. 
• Enters QC dates into CMS. 
• Coordinates QC work with departmental project team. 
• Participates in pre-study and progress meetings as needed. 
• Verifies accuracy of data tables and client data files. 
• Performs other related duties as assigned. 
Education / Qualifications 
• Bachelor of Science/Arts (BS/BA) degree. 
• Ability to efficiently use basic software (e.g., Word, Excel,PowerPoint). 
Experience 
• No previous experience required. 
• Experience with HPLC, GC, GC-MSD, or LC/MS instrumentation is helpful. 

职位要求：

专业要求：药学,生物学

最低学历：本科

工作年限：1-3年

职称要求：初级

地址：上海浦东新区伽利略路338号9号楼（有班车）

招聘岗位：GLP QA officer -生物分析（大小分子）             6k~12k/月               本科           经验不限

职位描述：

Responsibilities / Duties 
• Performs protocol, data, report, and in-lab phase inspections for aspecific study type to verify conformance to applicable SOP andregulatory requirements. 
• Evaluates responses to inspection reports and performs follow-up withrespondents, management, or others, if needed, to ensure resolution. 
• Ensures that systems used in QA are properly maintained (e.g., QAaudit records, training records). 
• Notifies management of service failures. 
• Manages all aspects of personal, daily micro-scheduling, organizationand prioritization related to a full workload. 
• Performs study sign-off including but not limited to QA statementpreparation (internal/external) and report finalization. 
• Performs SOP reviews for specific study type. 
• Starts to participate in internal facility and supplementalinspections, under supervision. 
• Starts to deliver basic quality/regulatory training, undersupervision. 
• Identifies opportunities for process improvement and harmonizationefforts that promote best practices. 
• Performs other related duties as assigned. 

Education / Qualifications 
• Bachelor of Science/Arts (BS/BA) degree; degree in a science field ispreferred (e.g. chemistry, biology, animal science) 

Experience 
• At least 2 years of experience as a quality auditor in a GxP-regulatedenvironment or at least three years working experience in GxP regulatedenvironment. 

职位要求：

专业要求：药学,生物学

最低学历：本科

工作年限：经验不限

职称要求：初级

地址：上海浦东新区伽利略路338号9号楼（有班车）

招聘岗位：临床医学检验Medical Technologist              5k~9k/月                 大专            经验不限

职位描述：

Responsibilities / Duties: 

♦ Perform assigned clinical laboratory testing accurately and in atimely manner. 
o Resolve pendings. Retrieve and check specimens against pending list.Document specimen discrepancies. Notify laboratory management whenspecimen discrepancies are not resolved. 
o Prepare workstation and instrumentation for the assigned testing. oProperly handle specimens and independently resolve technical specimenissues in preparation for analysis and specimen storage. Contactinternal customers for clarification as needed. 
o Operate instruments to perform testing in accordance with establishedwritten 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 ofestablished quality assurance and quality control procedures. 
o Perform experiments, as scheduled, for evaluation of new Calibratorand/or QC lots. Summarize results of investigations and compile data forreview by management. 
o Document quality control results. Interpret quality control resultsaccording to Westgard rules or other established departmental proceduresand accurately document biases, warnings and violations of controlvalues. 
o Document corrective action for unusual occurrences (e.g. QCviolations, 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 toSOPs. 
o Prepare and properly label reagent, quality control, calibratormaterial. 
o Document implementation of new reagents/materials according to SOPs. 
o Perform parallel testing, linearity’s, stability, other qualitycontrol practices needed to ensure validity of material prior to beingplaced into service. 
o Perform inventory control of supplies and reagents as approved bymanagement. 
♦ Result Entry (Auto-verification and manual entry). 
o When data is manually entered (e.g. QC, patient data) ensure peerreview is performed and documented prior to release of results. 
o Prepare proper documentation of test results and enter into theinformation system. 
o Generate an appropriate audit trail for all activities. 
o Document and communicate any result reporting problems orinconsistencies to laboratory management. 
o Complete testing within the expected turnaround time to meetcustomers’ expectations. 
♦ Ensures maintenance of instruments and equipment is performedaccording to manufacturer and SOP requirements, and documented accordingto SOP. o Calibrate instruments, equipment and/or assays as required anddocument. 
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 notmeet specifications. 
♦ Comply with regulatory guidelines and Covance Standard OperatingProcedures (SOPs) at all times. 
♦ Training 
o Individual is responsible for maintaining his/her complete up-to-datetraining file and is accountable for correcting and deficiencies foundin his/her training file. 
o Individual is responsible for ensuring he/she is trained and trainingis documented prior to performing a task. 
o The individual successfully completes, as scheduled, competencyassessment and ensures competency testing documentation is provided tomanagement for review/retention. 
o Competently performs department duties as set forth in the departmenttraining checklist(s). 
o May assist in training new employees and follows-up to ensure trainingis understood. 
o Attends, as scheduled, department, mandatory and other meetings andtraining, as required according to training matrices. 
♦ Work to achieve partnership with both internal customers and externalclients by: 
o Pull data in a timely manner for review by QA and external clients. 
o Contribute to the provision of accurate verbal or written response tointernal QA and client audit findings. Coordinate, where needed, withother resources to resolve issue. 
o Researches and prepares a response following investigation for qualitypurposes. Coordinate, where needed, with other resources to resolveissue. 
o Research and responds in a timely manner to internal customerinquiries regarding status of test results, retrieval of samples fortesting/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 precautionguidelines at all times. Maintains a clean, organized and safe workenvironment. Minimizes biohazard waste. Cleans workstation and materialsdaily. 
♦ Takes action for the department when additional responsibilities andopportunities are presented. 
♦ Provide laboratory management with a report of activities uponrequest. 
♦ Other duties as assigned. 

Education / Qualifications 

Required: 
• Individual must qualify as testing personnel under MoH regulations. 
 Preferred: 
• Bachelor's degree in Medical Technology or completion of at least a12-month training program in Medical Technology. 
 OR 
• Bachelor's degree in a chemical, physical or biological science froman accredited college or university and one year training and/orexperience in the specialty in which testing is to be performed. Suchtraining must be equivalent to that received in a school of MedicalTechnology. 


Experience 
1 year lab experience, chemistry department prefer. 

Location: 浦东新区张江伽利略路338号9号楼 


kay words: 血常规 免疫 生化 临检

职位要求：

专业要求：临床医学其他学科,医学生物化学

最低学历：大专

工作年限：经验不限

职称要求：初级

地址：上海浦东新区伽利略路338号9号楼（有班车）

招聘岗位：药代动力学研究员Scientist (DMPK)             6k~12k/月               本科                   经验不限

职位描述：

Responsibilities/Duties 
• Support DMPK in vitro and/or in vivo assays including assay design,biosample analysis, method development and validation and report forvarious compounds and components in compliance with appropriate SOPs andregulatory agency guidelines. 
• Support in setting up, validating, and conducting DMPK in vitroassays from protocol design, experiment, and report. 
• Support in conducting and coordinating DMPK in vivo projects fromprotocol design, experiment, and report. 
• Set up and performs method development and validation of variousanalytes in a variety of matrices with supervision. 
• Set up, maintain, operate and perform routine and non-routinemaintenance on general equipment, including problem identification andresolution. 
• Inform Study Director, Principal Investigator and/or management ofany problems and/or deviations that may affect the integrity of the dataand recommends corrective action. 
• Suggest and perform modifications to test methods or procedureswhere precedence exists. 
• Organize, conduct and evaluate analytical results and testing. 
• Performs QC review of data. 
• Maintain study documentation and laboratory records. 
• Promote a cohesive team environment. 
• Provide input and participate in project meetings, plans, monitorsand guides project work. 
• Maintain a clean and safe laboratory work environment. 
• Train and assist less experienced staff. 
• Participate in process improvement initiatives. 
• Participate in client visits as needed, assist in communicatingtechnical information. 
• Effectively plan and utilize personnel and resources for timelycompletion of assigned projects. 
• Assists in writing reports and protocols. 
• Writes SOPs and methods. 
• Assist in evaluation of data for incorporation into written reports. 
• Perform other related duties as assigned. 
Education/Qualifications 
• BS/BA degree in science plus at least 3 years or above experience orMS degree with 1 years or above experience in analytical chemistry,pharmacokinetics, or metabolism. 
Experience 
• 1 years or above experience in analytical chemistry, pharmacokinetics,or metabolism 
• Familiar with the use of standard laboratory equipment (e.g.,balances, pipettes, centrifuges). 
• Experience with use and trouble shooting of analytical equipment suchas LC-MS/MS. 
• Knowledgeable on a variety of study types, analysis procedures andmethodologies. 

职位要求：

专业要求：药学,生物学

最低学历：本科

工作年限：经验不限

职称要求：初级

地址：上海浦东新区康新公路3377号（有班车 ）

招聘岗位：生物分析研究员Scientist (Large Molecular)- BioA              6k~12k/月              本科                经验不限

职位描述：

The statements below reflect the general responsibilities andrequirements of the identified position but may not describe all thework requirements that may be inherent in the job. 

Job Summary: 
Analyzes biological or chemical samples and/or develops/validatesmethodologies for various compounds and components in compliance withappropriate standard operating procedures (SOPs) and regulatory agencyguidelines. 

Duties and Responsibilities: 
• Organizes, conducts and evaluates analytical results and testing. 
• Maintains study documentation and laboratory records. 
• Independently sets-up, maintains, operates and performs routine andnon-routine maintenance on general equipment, including problemidentification and resolution. 
• Performs quality control review of data. 
• Informs Study Director, Principal Investigator and/or management ofany problems and/or deviations that may affect integrity of the data;participates in corrective action of problems. 
• Promotes a cohesive team environment. 
• With supervisory assistance, assures technical staff compliance toSOPs and other regulatory agency guidelines. 
• Assists in setting up and performing method development and validationof various analytes in a variety of matrices. 
• Performs complex analyses using unfamiliar or new methods, asking forscientific guidance as needed. 
• Makes suggestions for modifications in test methods or procedures. 
• Provides input and participates in project meetings, plans, monitorsand guides project work. 
• With supervisory assistance, serves as a lead chemist on projects,overseeing a small group of technical staff. 
• Trains, mentors, and assists less experienced staff. 
• Maintains a clean and safe laboratory work environment. 
• Participates in new equipment and instrument assessment andqualification, as appropriate. 
• Participates in client visits as needed, assists in communicatingtechnical information. 
• Participates in process improvement initiatives. 
• Assists in evaluation of data for incorporation into written reports. 
• Effectively plans and utilizes personnel and resources for timelycompletion of assigned projects. 
• Assists in writing reports and protocols. 
• Writes SOPs and methods. 
• Performs other related duties as assigned. 


Education/Qualifications: 
• Minimum Bachelor of Science/Arts (BS/BA) degree in chemistry orrelated scientific field 
• Experience may be substituted for education. 
• Ability to perform advanced computer skills (e.g., Word, Excel). 
Experience: 
• 4 years related or relevant laboratory experience required with aBS/BA degree or 1 to 2 years’ experience with an MS degree. 
• Familiar with the use of standard laboratory equipment (e.g.,balances, pipettes, centrifuges). 
• Experience with use and trouble shooting of analytical equipment. 
• Effective communication (verbal and written), presentation andinterpersonal skills. 
• Ability to design and independently conduct tests for chemistryprojects and provide initial analysis of results. 
• Acts as technical resource for the department (trouble shooting,method development, qualification, maintenance and training). 
• Evaluates data for incorporation into written reports. 
• Advanced time management skills to complete project assignments ontime, with minimal or no supervision. 
• Able to effectively schedule resources. 
• Understands and helps staff with compliance to SOPs and otherregulatory agency guidelines. 
• Identifies process improvement opportunities, recommends solutions andimplements action plans. 
• Able to effectively communicate, both verbally and in writing. 
• Effectively interacts with internal and/or external clients. 
• Acts as a project leader. 
• Ability to assist in the preparation of relevant sections of finalreports. 
• Knowledgeable on a variety of study types, analysis procedures andmethodologies. 

职位要求：

专业要求：药学,生物学

最低学历：本科

工作年限：经验不限

职称要求：初级

地址：上海浦东新区伽利略路338号9号楼（有班车）

招聘岗位：项目协调员 Study coordinator（PM）                 6k~12k/月                本科               经验不限

职位描述：

Responsibilities / Duties 
• Independently drafts protocols, sample analysis outlines (SAOs),amendments and study schedules with some oversight, using proposaloutline or client-supplied information. 
• Responsible for report preparation, including table and figurepreparation. Compiles analytical information from laboratory groups. 
• Responsible for data table compilation including quality reviewoversight and data table transfer. 
• Communicates and interacts with study team, other departments andclients as applicable. 
• Serve as the primary contact in communication and interaction withother departments and clients as applicable. 
• Proven ability to plan, prioritize and manage workload and multipleresponsibilities. 
• Demonstrated ability to independently use project tracking systems asappropriate. 
• Maintains well documented, organized and up-to-date study filesincluding study schedule, protocol and correspondence as applicable. 
• Assists SD/PI in monitoring study progress. 
• Serves as a backup PI/SD on project management tasks 
• Schedules study phases in coordination with SD/PI and lab operations. 
• Proven ability to participate in and assist Study Director/PrincipalInvestigators with pre-initiation and other study related meetings asrequired. 
• Proven ability to manage increasingly complex projects and studydesigns and/or increased study load. 
• Demonstrated capability to manage work for key clients. 
• Demonstrated ability to support and be involved in process improvementinitiates and endeavors 
• Reviews QAU report audits. Submits audit responses for approval asappropriate. Follows up with appropriate personnel to ensure that allnecessary report/raw data clarifications are completed within specifiedtimelines. 
• Assists with routine client visits as requested. 
• Performs other related duties as assigned 
Education / Qualifications 
1. Bachelor of Science (BS) degree in science or related field. 
2. Experience may be substituted for education. 
3. Ability to utilize word processing software, database, spreadsheet,and specialized software. 
Experience 
1. Minimum of 3 years of related experience. 
2. Excellent communication, presentation, and interpersonal skills. 
3. Excellent attention to detail. 
4. Ability to prioritize and manage time. 

职位要求：

专业要求：药学,生物学

最低学历：本科

工作年限：经验不限

职称要求：初级

地址：上海浦东新区伽利略路338号9号楼（有班车）

招聘岗位：药效制剂研究员 Study Technician Dose Form             5k~8k/月              大专                经验不限

职位描述：

Responsibilities / Duties: 
• Reviews and interprets study protocol for test material formulationprocedures and to ensure that a study tasks are conducted according withprotocol, SOPs, and GLPs. 
• Collects and records applicable hand and computer generated data inaccordance with protocol, SOPs, and GLPs. 
• Performs study calculations and specific techniques for test materialformulation. 
• Serves as Lead Tech and is responsible for study set up (includingpreparation of mix procedures) and management, data organization, QAaudit response, internal and external client communication skills, andquality check procedures. Participates in pre-initiation meetings. 
• Learns to interact with Study Directors and management to preparevehicle and test material mix procedures. 
• Learns to identify problems, determine appropriate actions andimplement solutions. 
• Responsible to review study schedule and ensure that it is completeand accurate according to protocol requirements. Communicates necessarychanges to supervisor. 
• Uses laboratory equipment appropriate for assigned tasks. 
• Prepares laboratory reagents, vehicles, diets, solution/suspensions,and capsules according to study protocols and SOPs. 
• Performs the process of disposition of samples from prepared dosematerials by Covance or sponsor. 
• Performs formulation verification and storage of prepared testmaterials. 
• Responsible for safe handling of test materials. 
• Maintains a clean and safe work environment. 
• Recognizes deviations from normal results and informs Study Director,Principal Investigator, or management of any problems and/or deviationsthat may affect the integrity of the data. 
• Able to adapt techniques to new procedures or particular needs asdirected. 
• May train and instruct less experienced staff. Guides and supportssecondary tech in study management responsibilities. 
• Plans assigned workload on a daily basis and effectively schedulesmultiple assignments. 
• Contributes to a cohesive team environment. Plans individual workloadin coordination with team members. 
• Identifies and participates in process improvement initiatives. 
• Performs other related duties as assigned 
Education / Qualifications 
• Bachelor of Science/Arts (BS/BA) degree in chemistry or relatedscientific field 
• Experience may be substituted for education. 
• Ability to perform basic computer skills (e.g., Word, Excel). 
Experience: 
• 6 months to 1 year related experience. 

职位要求：

专业要求：药学,生物学

最低学历：大专

工作年限：经验不限

职称要求：初级

地址：上海浦东新区康新公路3377号

招聘岗位：动物实验员                5k~8k/月              大专                经验不限

职位描述：

Job Posting 
• The scope of this position is within one site across multiple studiesdaily. 
• Learns how to determine and document clinical observations, bodyweight data, food consumption data environmental data, and other data onthe appropriate data collection system (or by hand when necessary). 
• Learns how to interpret a protocol. 
• Learns study management, data organization, QA audit response,internal and external client communication skills, and quality checkprocedures. 
• Learns how to ensure that a study is conducted according to protocol,SOPs, IACUC and government regulations. 
• Learns how to perform basic dosing techniques and restraintprocedures. 
• Maintains animal rooms and equipment in compliance with GLP and AAALACrequirements. 
• Learns commonly used clinical sampling techniques. Learns how toprocess and package biological samples for shipment to client. 
• Receive, donate and euthanize animals according to AVMA guidelines. 
• Recognizes deviations from expected results and takes appropriateaction. 
• Able to adapt techniques to new procedures or particular needs asdirected. 
• Effectively schedules multiple assignments. 
• Maintains well documented laboratory records according to GLPs.Reviews own data and identifies potential problems. 
• Learns to utilize computer software for forms and proceduregeneration. 
• May instruct less experienced staff. 
• Learns blood pressure and body temperature measurement procedures asappropriate. 
• Reports all animal care concerns and becomes involved in theresolution and appropriate corrective action, when necessary. 
• May be involved in client tours or client interaction during studyinitiations. 
• Other duties as assigned. 

Education / Qualifications 

• Bachelor degree in Life Sciences, Associate degree in LaboratoryAnimal Technology, or Associate degree in Veterinary Technology with 0-2years of related experience. 
• AALAS certification at Laboratory Animal Technician level desirable. 


Experience 
• No experience is required if you meet the education requirements. 
• 0-2 years of related external experience based on education. 
• A minimum of 6 months experience as a Study Tech Trainee whileemployed at Covance, or a minimum of two years of related experience maybe substituted for education requirements 

职位要求：

专业要求：畜牧、兽医科学,生物学

最低学历：大专

工作年限：经验不限

职称要求：初级

地址：上海浦东新区康新公路3377号查看地图

招聘岗位：生物分析样本管理员 (Sample Coordinator)              5k~8k/月                大专            经验不限

职位描述：

Duties and Responsibilities: 
Responsibilities / Duties: 
Laboratory Pre-Analytical Services 
1. Ensure proper temperature of specimens are maintained 
2. Ensure timely processing of kits and requisitions 
3. Ensure all testing requested is ordered 
4. Ensure timely delivery of specimens to the Laboratory 
5. Ensure timely communication with departments/clients concerningprocessing problems 
6. Ensure sufficient documentation of all processes 
Specimen Management 
1. Ensure that specimens are picked up from Laboratory Pre-AnalyticalServices, sorted and pre-scanned into the appropriate temperature binsin a timely fashion. 
2. Responsible for registration and processing of specimens into correctstorage temperature 
3. Generation and application of specialized labels to include minilabels and computer generated bar codes. 
4. Process, register, package and ship samples requiring specialhandling 
5. Research and resolution of problem samples and correct routing ofthese specimens maintaining documentation during the process. 
6. Accountable for accurately identifying specimens that need to bediscarded and completing the discard process 
7. Perform domestic and/or in-house shipping procedures. 
8. Maintain inventory records for items used in daily workflow. 
9. Consolidate and move drawers as specified to effectively utilizefreezer space. 
10. Freezer maintenanceGeneral responsibilities 

General responsibilities 
Follow SOPs to guarantee compliance, uniformity, and standardization ofmethods 
Incumbent is responsible for maintaining their complete up-to-datetraining file. 

Nonessential Functions 
Other duties as assigned 

Education/Qualifications: 
Good level of general education (e.g. Diploma or Bachelor of Sciencedegree) in Life science or related studies is preferred but notessential 

Experience 
Previous healthcare, medical or laboratory experience is preferred butnot essential

职位要求：

专业要求：生物学,药学

最低学历：大专

工作年限：经验不限

职称要求：初级

地址：上海浦东新区伽利略路338号9号楼（有班车）