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ZSHK Laboratories Limited Shatin Area Posted on 17-Mar-23 Apply Now Apply Now pharmological research leader
ZSHK Laboratories Limited Apply Now Job Highlights
• Attractive remuneration, benefits and prospect
• PhD’s degree in Pharmacology or medicine
• On-the-job training
Job Description
Located in HKSTP, the Drug Safety Testing Centre (DSC) aims to facilitate the translation of promising therapeutics and medical devices from the pre-clinical phase to the clinical stage. This first of its kind facility adheres to the highest international and industry standards, including AAALAC and Good Laboratory Practices (GLP), which is an international standard prescribing a set of rigid and quality criteria for conducting studies, data collection and reporting. It defines how preclinical data is required and accepted by... different regulatory authorities (for example, China NMPA, US FDA and OECD). The facility commits to provide the GLP-compliant preclinical services on toxicology, genotoxicity, toxicokinetics, safety pharmacology, reproductive toxicology, ADME etc for facilitating the development of new drug.

Responsibilities:
• Supervise animal lab technicians to ensure all the routine works including husbandry, cleaning, disinfection and operations in lab run smoothly.
• Conduct traing on technical skills and competencies,performing traing evaluations to ensure the staffs are well-trained and qualified in handing animals and performing experiments.
• Protocol development according to the sponsor's requirments and discuss with the sponsors with their projects.
• Design and develop various animal models for the study plan according to the requirements of sponsors.
• Coordinate with all the departments to ensure the study plans are smoothly carried out. Qualifications:
• Applicants should possess a PhD’s degree in Pharmacology or medicine equivalent.
• Ample experience (over 5 years)in handling animals, familiar with animal behaviors including using different animal models for studies, designing experimental plan protocol, performing experiments, writing reports and discussing/delivering results.
• Communication skills and management skills(including staff and tasks)are needed to be acquired. Additional Information
Career Level Senior Years of Experience 5 years Job Type Full Time, Permanent, Contract Job Functions Sciences, Lab, R&D , Laboratory , Research & Development (R&D) , Others Company Overview

滬港中科國際生物科技有限公司（ ZSHK Laboratories Limited ）總部位於中國香港特別行政區。滬港中科公司 以 香港特別行政區的國際化人才和扎實的科技發展優勢，在香港科技園、廣東省深圳市坪山區、江蘇省蘇州工業園區都建有獨立實驗 設 施。公司以生物醫藥和醫療器械的臨床前研究評價服務為主，業務內容包括藥理藥效研究、藥物代謝動力學研究和安全性評價研究的一站式研發服務平臺，以滿足國際申報要求為目標，立志成為中國生物醫藥與醫療器械研發企業，在全球發展和拓展中成為最有價值的研發合作夥伴。 滬港中科公司目前在蘇州工業園營運 3000 平方米的藥物臨床前評價服務實驗 設 施（安領生物醫藥（蘇州）有限公司）和深圳坪山區 9400 平方米的新藥與醫療器械評價實驗 設 施（安領生物醫藥（深圳）有限公司） ，並與 香港科技園建設 2000 平方米的藥物評價實驗 設 施。這些實驗室都將具備中國藥品監督管理總局（ NMPA ）和歐盟 OECD 的 GLP 資格認證資格。未來三年，滬港中科公司 將成為具有總面積達 35000 平方米的實驗 設 施、藥物與醫療器械臨床前評價、國內外註冊申報服務、新藥臨床研究服務、全球專利授權法律服務等全方位一體化研發服務的國際企業 。

Headquartered in Hong Kong, ZSHK Laboratory Limited is established by the core team of the Safety Evaluation Center of the Shanghai Institute of Materia Medica, Chinese Academy of Sciences. The company focuses on preclinicalresearch and evaluation services for biopharmaceutical and medical devices. We provide a one-stop R&D platform for pharmacological efficacy research, pharmacokinetics research and safety evaluation research to meet the rigid requirement from global pharmaceuticalregulatory bodies. Determined to become a Chinese biopharmaceutical and medical device R&D enterprise, and become the most valuable R&D partner in global development and expansion, the company operates a 3,000 sq.m preclinical drug evaluation service facilityin Suzhou Industrial Park (Anling Biomedical (Suzhou) Co., Ltd.) and a 9,400 sq.m new drug and medical device evaluation laboratory in Pingshan District, Shenzhen (Anling Biomedical (Shenzhen) Co., Ltd.), and is collaborating with Hong Kong Science and TechnologyPark Corporation to establish a 2,000 sq.m drug evaluation facility All these facilities will be certified with the GLP qualifications from National Medical Products Administration (NMPA) and the European Union OECD. ZSHK strives to provide a comprehensiveintegration of more than 35,000 sq.m facilities for pre-clinical evaluation of drugs, biopharmaceutical products and medical devices for domestic and foreign registration and declaration services, clinical research services for new drugs, and legal servicesfor global patent authorization.
Additional Company Information
Industry Medical/Pharmaceutical Benefits & Others Dental insurance, Double pay, Life insurance, Medical insurance, Performance bonus, Five-day work week, Flexible working hours More jobs from this employer Report this job ad Job seekers Browse jobs Post resumes Job alerts Profile Career insights Employers Post a job ad Search candidates Advertise with us Best companies About JobsDB About us Career @ SEEK Asia (JobsDB) Contact Contact us FAQ Hong Kong Privacy statement Terms & conditions Copyright © 1998-2023, JobsDB
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