諾佛葛生技顧問股份有限公司
(Senior) Scientist_Lab-Small Molecular
10/11 Updated
Array
Full-time
Mid to Senior Level
Salary & Location
Salary negotiable
(Regular monthly salary of NT$40,000 or above)
台北市南港區
Required
Language Requirements
English
聽/中等、說/中等、讀/中等、寫/中等
Chinese
聽/精通、說/精通、讀/精通、寫/精通
Work Experience
1年以上
Job Description
Please do submit English resume via our company website.
https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2284?utm_medium=jobboard
Reporting to:
Lab Director, or Lab Manager
Position Description:
The Researcher is responsible for the conduct of analysis related works according to GCP, GLP, CAP, Standard Operating Procedures (SOP), applicable Study Specific Procedures (SSP), and local regulatory requirements.
The report writer/QC is responsible for writing correspond study report/method according to study plan and Standard Operating Procedures (SOP). And to perform the quality control works.
Responsibilities:
General Responsibilities
• Conduct analysis work following related SOPs and guidance.
• Draft/check/review/approve documents, such as SOP, protocol, analytical result, report and method.
• Involve in lab logistics (general affair) management, such as purchasing, inventory controlling, payment applying.
• Responsible for instrument maintenances, workspace cleaning/maintenance.
• Delegated /assigned as the system owner for computerized system, do the corresponding work for system, such as validation test, periodic review, report, etc.
• Participate in CAP/GCP/GLP/ regulatory related training courses.
• Provide temporary supporting assigned by line manager.
• Refer to additional Study Based Responsibilities while being assigned in analytical project.
• Involve in sample collection kit/label preparation.
• Involve in analytical study project management.
• Other tasks assigned by line manager.
Study Based Responsibility (if needed)
Study Personnel in Study
• All personnel involved in the conduct of the study must be knowledgeable in those parts of the Principles of Good Laboratory Practice which are applicable to their involvement in the study.
• Study personnel will have access to the study plan and appropriate Standard Operating Procedures applicable to their involvement in the study. It is their responsibility to comply with the instructions given in these documents. Any deviation from these instructions should be documented and communicated directly to the Study Director, and/or if appropriate, the Principal Investigator(s).
• All study personnel are responsible for recording raw data promptly and accurately and in compliance with these Principles of Good Laboratory Practice, and are responsible for the quality of their data.
• Study personnel should exercise health precautions to minimize risk to themselves and to ensure the integrity of the study. They should communicate to the appropriate person any relevant known health or medical condition in order that they can be excluded from operations that may affect the study.
Report Writer/Quality Control
• As QC person, check and review the study data, document, report.
• Involve in reference compound management, such as planning, shipping, receiving, using, storing, and disposing. And as the backup of sample manager.
Qualifications:
Education and Experience:
• Secondary Technical school, Junior colleague, BS (Bachelor of Science) degree in Biochemistry, Biotechnology and Laboratory Science, Chemistry, or a related field. Advanced degree is a plus for Associate Researcher/ Senior Researcher.
• License of Medical Technician is required for Associate Researcher/ Senior Researcher in Central Lab.
Skills and Competencies:
• Familiar with all lab operation activities.
• Good working knowledge of CAP/GCP/GLP, applicable law (local and country) and regulatory requirements.
• Good communication skills.
• Good verbal and written English or other second language skills.
• Good problem-solving skills.
• Effective time management and prioritization skills.
Number of Openings
1~2人
Educational Requirements
大學(學院)以上
Work Schedule
日班
Leave Policy
週休二日
Job Skills
Operation of Chemical Detection Instruments
Laboratory Equipment Operation
Interpretation of Inspection and Examination Report Results
Chemical Analysis Capability
化學檢測儀器操作 實驗室設備操作 檢查及檢驗報告結果判讀 化學分析能力
Job Category
Biotechnology Research and Development Staff
Pharmaceutical Research and Development Staff
Pathology and Pharmacology Research Staff
台北市中山區
其他醫療保健服務業
Novotech is internationally recognized as the leading regional full-service contract research organization (CRO) in Asia-Pacific providing clinical development services across all clinical trial phases and therapeutic areas, including an in-house and integrated global product development and regulatory affairs consultancy, BioDesk.
Working in a fast paced and adaptable environment, we set a high benchmark for clinical trial operations by listening carefully, allocating Asia Pacific’s best people and talent, and leveraging best in class platforms, technology, systems and processes to meet our client’s clinical program goals and ultimately improve patient lives.
Our people are critical in meeting organisational and client’s objectives and we place a strong emphasis on creating an inclusive, collaborative, transparent and collegiate work environment where everyone is supported to be the best they can be. We support our employees with financial assistance to enable flexible working arrangements, paid parental leave for primary and secondary carers, and regular training, learning, and international knowledge-sharing opportunities.
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