諾佛葛生技顧問股份有限公司
Researcher/Scientist_Lab-Large Molecule
9/18 Updated
Array
Full-time
Senior Level
11 ~ 30 applicants

Salary & Location

Monthly SalaryNT$ 50,000~75,000
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
3年以上

Job 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. Manage the operation of MT and aid physicians in the diagnosis, treatment, and prevention of diseases by testing patient specimens, correlating data, and reporting results in a timely manner to effect quality patient care.
Responsibilities:
Perform analysis work according to SOPs and guidance.
Prepare, review, and approve various documents, including SOPs, protocols, reports, and analytical methods.
Manage lab logistics, including purchasing, inventory control, and payment processing.
Maintain instruments and ensure cleanliness and maintenance of the workspace.
Take on the role of system owner for computerized systems, performing tasks such as validation tests, periodic reviews, and reporting.
Attend training courses related to CAP/GCP/GLP/regulatory requirements.
Study Based Responsibility (if needed)
Analytical Study Director in Study
Work as the Study Director, responsible for the overall conduct and final report of the study.
Approve the study plan and any amendments by signature, and ensure Quality Assurance personnel receive timely copies.
Make study plans, amendments, and SOPs available to study personnel.
Ensure procedures in the study plan are followed and document deviations and take corrective action if necessary.
Document and record all generated raw data.
Validate computerized systems used in the study, sign and date the final report to indicate acceptance of responsibility for data validity, and ensure study materials are archived after completion.
Study Personnel in Study
Ensure personnel are knowledgeable in relevant Principles of Good Laboratory Practice.
Provide study personnel with access to study plans and SOPs applicable to their involvement, with a responsibility to follow instructions and document any deviations.
Emphasize the responsibility of all study personnel to promptly and accurately record raw data, comply with Good Laboratory Practice principles, and exercise health precautions to safeguard the integrity of the study.
Number of Openings
1~2人
Educational Requirements
大學(學院)以上
Work Schedule
日班
Leave Policy
依公司規定

Job Skills

Operation of Chemical Detection Instruments
Laboratory Equipment Operation
Interpretation of Inspection and Examination Report Results
Chemical Analysis Capability
Conducting Pharmacognosy and Pharmacy Research and Development
Drug Analysis and Pharmacognosy
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 進行生藥與藥學研究發展 藥物分析與生藥學
Job Category
Biotechnology Research and Development Staff
Pharmaceutical Research and Development Staff
Pathology and Pharmacology Research Staff
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.
11 ~ 30 applicants