13 Pharmaceutical Research jobs in Hong Kong

Join to apply for the Research Scientist role at Absolute Pure EnviroSci Limited .

We are undertaking an innovative project to develop a biodegradable, non-woven wound dressing using advanced electrospinning technology. This nanofiber dressing aims to enhance wound healing, manage moisture effectively, and reduce environmental impact by replacing non-biodegradable materials in traditional wound care products.

Responsibilities include:

• Conduct experiments on biodegradable polymers and functional additives.
• Optimize electrospinning process parameters using DoE statistics.
• Collaborate with a multidisciplinary team to evaluate product performance and environmental impact.
• Document experiments and contribute to scientific reports.

Additional details:

• Seniority level: Associate
• Employment type: Full-time
• Job function: Science, Engineering, and Science

This position is based in Hong Kong SAR. Apply now to join this exciting project and contribute to sustainable healthcare innovations.

Join to apply for the Research Scientist (p1.1-1.3) role at Centre for Advances in Reliability and Safety

1 year ago Be among the first 25 applicants

Join to apply for the Research Scientist (p1.1-1.3) role at Centre for Advances in Reliability and Safety

CENTRE FOR ADVANCES IN RELIABILITY AND SAFETY LIMITED

Centre for Advances in Reliability and Safety Limited (CAiRS), initiated by The Hong Kong Polytechnic University, is established in 2020 with its operation located in the Hong Kong Science Park, New Territories, Hong Kong. The mission of CAiRS is to link up academic and industrial counterparts to introduce and implement new artificial intelligence methods and deep learning techniques with reliability modelling, with the goal of improving the products reliability and systems safety of critical components and devices, products, systems and sub-systems designed, commissioned and/or manufactured by Hong Kong companies and enterprises.

Research Scientist (Ref. No.: CAiRS-RS/P1.1-3)

(Appointment period: each for twenty-four months initially, with possibility of further appointment)

Required

The appointees will report to the Programme Manager and assist in planning and monitoring one or two of the research projects - “Informative feature discovery and selection”, “Early detection of degradation in electronic interconnects” and “Anomaly detection for systems under indeterminate operating conditions” in the areas of electrical reliability and safety, machine learning, and computer vision. They will be required to:

• develop objectives and design projects and proposals;
• coordinate and monitor research projects;
• formulate and implement appropriate methodologies for research projects;
• conduct experiments, perform data analysis, and evaluate test and research results;
• supervise project team members;
• compose research findings for publications, grants, and other documents;
• assist in grant and manuscript submissions; and
• perform any other duties as assigned by the Centre Director or his delegate
  
  

• a master’s degree or above in Science, Engineering or a relevant discipline;
• at least two years of research-related experience in the fields of electrical reliability/safety, machine learning and computer vision;
• knowledge and understanding of related research methodologies; and
• experience in research publications and grant applications.
  
  

• Seniority level Not Applicable

• Employment type Other

• Job function Other
• Industries Research Services

Referrals increase your chances of interviewing at Centre for Advances in Reliability and Safety by 2x

Get notified about new Research Scientist jobs in Shek O, Hong Kong SAR .

Tai Po District, Hong Kong SAR HK$20,000.00-HK$5,000.00 4 weeks ago

Tai Po District, Hong Kong SAR HK 30,000.00-HK 50,000.00 1 week ago

Sha Tin District, Hong Kong SAR 1 month ago

New Territories, Hong Kong SAR 2 weeks ago

Yuen Long District, Hong Kong SAR 2 weeks ago

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Join to apply for the Research Scientist (p1.1-1.3) role at Centre for Advances in Reliability and Safety

1 year ago Be among the first 25 applicants

Join to apply for the Research Scientist (p1.1-1.3) role at Centre for Advances in Reliability and Safety

CENTRE FOR ADVANCES IN RELIABILITY AND SAFETY LIMITED
Centre for Advances in Reliability and Safety Limited (CAiRS), initiated by The Hong Kong Polytechnic University, is established in 2020 with its operation located in the Hong Kong Science Park, New Territories, Hong Kong. The mission of CAiRS is to link up academic and industrial counterparts to introduce and implement new artificial intelligence methods and deep learning techniques with reliability modelling, with the goal of improving the products reliability and systems safety of critical components and devices, products, systems and sub-systems designed, commissioned and/or manufactured by Hong Kong companies and enterprises.
Research Scientist (Ref. No.: CAiRS-RS/P1.1-3)
(Appointment period: each for twenty-four months initially, with possibility of further appointment)
Required
The appointees will report to the Programme Manager and assist in planning and monitoring one or two of the research projects - “Informative feature discovery and selection”, “Early detection of degradation in electronic interconnects” and “Anomaly detection for systems under indeterminate operating conditions” in the areas of electrical reliability and safety, machine learning, and computer vision. They will be required to:

• develop objectives and design projects and proposals;
• coordinate and monitor research projects;
• formulate and implement appropriate methodologies for research projects;
• conduct experiments, perform data analysis, and evaluate test and research results;
• supervise project team members;
• compose research findings for publications, grants, and other documents;
• assist in grant and manuscript submissions; and
• perform any other duties as assigned by the Centre Director or his delegate
  

• a master’s degree or above in Science, Engineering or a relevant discipline;
• at least two years of research-related experience in the fields of electrical reliability/safety, machine learning and computer vision;
• knowledge and understanding of related research methodologies; and
• experience in research publications and grant applications.
  

• Seniority level Not Applicable

• Employment type Other

• Job function Other
• Industries Research Services

Referrals increase your chances of interviewing at Centre for Advances in Reliability and Safety by 2x

Get notified about new Research Scientist jobs in Shek O, Hong Kong SAR .

Tai Po District, Hong Kong SAR HK$20,000.00-HK$5,000.00 4 weeks ago

Tai Po District, Hong Kong SAR HK 30,000.00-HK 50,000.00 1 week ago

Sha Tin District, Hong Kong SAR 1 month ago

New Territories, Hong Kong SAR 2 weeks ago

Yuen Long District, Hong Kong SAR 2 weeks ago

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Join to apply for the Research Scientist (TCM | Traditional Chinese Medicine) role at Vita Green

1 week ago Be among the first 25 applicants

Join to apply for the Research Scientist (TCM | Traditional Chinese Medicine) role at Vita Green

Ready to shape the future of Health and Wellness?

At Vita Green, we are all about creating a healthier, happier world, and we want you to be part of it!

About Vita Green Group

Vita Green stands at the forefront of the health supplements industry, committed to enhancing well-being through innovative research and cutting-edge solutions. Our GMP and HACCP-certified facilities ensure top-tier quality control at every step—from sourcing premium raw materials to advanced R&D—guaranteeing excellence in every product.

With a diverse portfolio of established brands and over 150 products, we continually expand and reach markets worldwide. At Vita Green, we uphold the highest standards, paving the way for a healthier future.

About the Job

You will be working in a growing department with a team of professionals. You will be involved in the planning and execution of pharmaceutical development programs for the company, and to develop market-driven innovative technology for the company. You will also acquire an understanding of the scientific knowledge and technical know-how required for pharmaceutical advanced formulation technology. You will build up strength in the competitive environment of both local and global pharmaceutical industries.

Key Responsibilities

• Participate in the innovative breakthrough in the modernization of traditional Chinese medicines.
• Develop and optimize micronization technologies, formulation techniques and process engineering for novel preparation of Chinese medicines.
• Perform formulation characterization such as moisture content, particle size analysis, microscopic observation, content assay and dissolution experiment.
• Manage research projects, including but not limit to timeline management, scope management and data organization.
• Communication with other departments and stakeholders in performing new product development projects and research projects.
• Opportunity to work with team manager and market leader in the registration of products in HongKong

Requirements

PhD or Master’s in Chinese Medicines, Chemistry, Pharmacy in Chinese Medicine, Pharmacology, Biochemistry, Biomedical Science, Translational Medicines, Material Science, Food and Nutritional Science, Chemical Engineering or relevant discipline.

• >3 years experiences in research projects, preferably in the Chinese medicines area. Experience in TCM micronization, nanotechnology or formulation technology is highly preferred.
• Analytical skills such as inspection of marker components by HPLC, LC-MS is a plus.
• Possess knowledge in Chinese medicines.
• Good communication skills. Good cultural fit to local research environment.
• Background knowledge in the treatment method of traditional Chinese Medicines is a
• plus.Possess can-do attitude, positive mind-set, team spirit and strong problem solving skill
• A stimulating career opportunity with the market leader
• Work comfortably and confidently in our fun and welcoming environment with a casual attire
• Convenient free shuttles from multiple locations.
• Fast track your career with our performance-based growth opportunities
• Performance-based bonuses offered at our discretion
• Comprehensive medical coverage available from day one under our company's medical insurance
• Competitive salary depending on experience.

• Seniority level Entry level

• Employment type Full-time

• Job function Research, Manufacturing, and Analyst
• Industries Pharmaceutical Manufacturing, Food and Beverage Manufacturing, and Biotechnology Research

Referrals increase your chances of interviewing at Vita Green by 2x

Get notified about new Research And Development Specialist jobs in Tai Po District, Hong Kong SAR .

Shenzhen, Guangdong, China CN¥10,000.00-CN¥5,000.00 2 years ago

Shenzhen, Guangdong, China CN 8,000.00-CN 6,000.00 2 years ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Join to apply for the Research Scientist (TCM | Traditional Chinese Medicine) role at Vita Green

1 week ago Be among the first 25 applicants

Join to apply for the Research Scientist (TCM | Traditional Chinese Medicine) role at Vita Green

Ready to shape the future of Health and Wellness?

At Vita Green, we are all about creating a healthier, happier world, and we want you to be part of it!

About Vita Green Group

Vita Green stands at the forefront of the health supplements industry, committed to enhancing well-being through innovative research and cutting-edge solutions. Our GMP and HACCP-certified facilities ensure top-tier quality control at every step—from sourcing premium raw materials to advanced R&D—guaranteeing excellence in every product.

With a diverse portfolio of established brands and over 150 products, we continually expand and reach markets worldwide. At Vita Green, we uphold the highest standards, paving the way for a healthier future.

About the Job

You will be working in a growing department with a team of professionals. You will be involved in the planning and execution of pharmaceutical development programs for the company, and to develop market-driven innovative technology for the company. You will also acquire an understanding of the scientific knowledge and technical know-how required for pharmaceutical advanced formulation technology. You will build up strength in the competitive environment of both local and global pharmaceutical industries.

Key Responsibilities

• Participate in the innovative breakthrough in the modernization of traditional Chinese medicines.
• Develop and optimize micronization technologies, formulation techniques and process engineering for novel preparation of Chinese medicines.
• Perform formulation characterization such as moisture content, particle size analysis, microscopic observation, content assay and dissolution experiment.
• Manage research projects, including but not limit to timeline management, scope management and data organization.
• Communication with other departments and stakeholders in performing new product development projects and research projects.
• Opportunity to work with team manager and market leader in the registration of products in HongKong

Requirements

PhD or Master’s in Chinese Medicines, Chemistry, Pharmacy in Chinese Medicine, Pharmacology, Biochemistry, Biomedical Science, Translational Medicines, Material Science, Food and Nutritional Science, Chemical Engineering or relevant discipline.

• >3 years experiences in research projects, preferably in the Chinese medicines area. Experience in TCM micronization, nanotechnology or formulation technology is highly preferred.
• Analytical skills such as inspection of marker components by HPLC, LC-MS is a plus.
• Possess knowledge in Chinese medicines.
• Good communication skills. Good cultural fit to local research environment.
• Background knowledge in the treatment method of traditional Chinese Medicines is a
• plus.Possess can-do attitude, positive mind-set, team spirit and strong problem solving skill
• A stimulating career opportunity with the market leader
• Work comfortably and confidently in our fun and welcoming environment with a casual attire
• Convenient free shuttles from multiple locations.
• Fast track your career with our performance-based growth opportunities
• Performance-based bonuses offered at our discretion
• Comprehensive medical coverage available from day one under our company's medical insurance
• Competitive salary depending on experience.

• Seniority level Entry level

• Employment type Full-time

• Job function Research, Manufacturing, and Analyst
• Industries Pharmaceutical Manufacturing, Food and Beverage Manufacturing, and Biotechnology Research

Referrals increase your chances of interviewing at Vita Green by 2x

Get notified about new Research And Development Specialist jobs in Tai Po District, Hong Kong SAR .

Shenzhen, Guangdong, China CN¥10,000.00-CN¥5,000.00 2 years ago

Shenzhen, Guangdong, China CN 8,000.00-CN 6,000.00 2 years ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Direct message the job poster from Tigermed

1.1 This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations.

1.2 The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

2.Responsibilities

(a) Site management

•Study site selection, initiation (SIV) and clinical monitoring.

•Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

•Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

•Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

•Track study recruitment to ensure recruitment target is achieved in all studies.

•Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.

•Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

•Assemble site specific EC submission dossier, and ensure submission to EC.

Training

•Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.

•Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

•Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

•Prepare/complete study records’ archiving according to protocol and sponsor requirements.

(b) Drug Safety

•Ensure safety information is disseminated to all sites according SOP and applicable regulations.

•Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

•Finalize budget and obtain signed contract from site, prior to site initiation visit.

•Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

•Update and maintain Study tools/systems in a timely manner.

3. Qualifications

3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. The excellent candidates will not be restricted to the current requirements;

3.2 At least 1 year of CRA experience;

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

• Seniority level Associate

• Employment type Full-time

• Job function Research
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Tigermed by 2x

Get notified about new Clinical Research Associate jobs in Hong Kong, Hong Kong SAR .

Islands District, Hong Kong SAR 11 hours ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Direct message the job poster from Tigermed

1.1 This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations.

1.2 The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

2.Responsibilities

(a) Site management

•Study site selection, initiation (SIV) and clinical monitoring.

•Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

•Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

•Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

•Track study recruitment to ensure recruitment target is achieved in all studies.

•Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.

•Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

•Assemble site specific EC submission dossier, and ensure submission to EC.

Training

•Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.

•Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

•Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

•Prepare/complete study records’ archiving according to protocol and sponsor requirements.

(b) Drug Safety

•Ensure safety information is disseminated to all sites according SOP and applicable regulations.

•Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

•Finalize budget and obtain signed contract from site, prior to site initiation visit.

•Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

•Update and maintain Study tools/systems in a timely manner.

3. Qualifications

3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. The excellent candidates will not be restricted to the current requirements;

3.2 At least 1 year of CRA experience;

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

• Seniority level Associate

• Employment type Full-time

• Job function Research
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Tigermed by 2x

Get notified about new Clinical Research Associate jobs in Hong Kong, Hong Kong SAR .

Islands District, Hong Kong SAR 11 hours ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

3 days ago Be among the first 25 applicants

Direct message the job poster from Tigermed

1.1 This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations.

1.2 The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

2.Responsibilities

(a) Site management

•Study site selection, initiation (SIV) and clinical monitoring.

•Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

•Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

•Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

•Track study recruitment to ensure recruitment target is achieved in all studies.

•Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.

•Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

•Assemble site specific EC submission dossier, and ensure submission to EC.

Training

•Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.

•Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

•Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

•Prepare/complete study records’ archiving according to protocol and sponsor requirements.

(b) Drug Safety

•Ensure safety information is disseminated to all sites according SOP and applicable regulations.

•Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

•Finalize budget and obtain signed contract from site, prior to site initiation visit.

•Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

•Update and maintain Study tools/systems in a timely manner.

3. Qualifications

3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. The excellent candidates will not be restricted to the current requirements;

3.2 At least 1 year of CRA experience;

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

• Seniority level Associate

• Employment type Full-time

• Job function Research
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Tigermed by 2x

Islands District, Hong Kong SAR 2 weeks ago

Kwai Tsing District, Hong Kong SAR 2 weeks ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

3 days ago Be among the first 25 applicants

Direct message the job poster from Tigermed

1.1 This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations.

1.2 The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

2.Responsibilities

(a) Site management

•Study site selection, initiation (SIV) and clinical monitoring.

•Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

•Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

•Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

•Track study recruitment to ensure recruitment target is achieved in all studies.

•Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.

•Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

•Assemble site specific EC submission dossier, and ensure submission to EC.

Training

•Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.

•Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

•Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

•Prepare/complete study records’ archiving according to protocol and sponsor requirements.

(b) Drug Safety

•Ensure safety information is disseminated to all sites according SOP and applicable regulations.

•Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

•Finalize budget and obtain signed contract from site, prior to site initiation visit.

•Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

•Update and maintain Study tools/systems in a timely manner.

3. Qualifications

3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. The excellent candidates will not be restricted to the current requirements;

3.2 At least 1 year of CRA experience;

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

• Seniority level Associate

• Employment type Full-time

• Job function Research
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Tigermed by 2x

Islands District, Hong Kong SAR 2 weeks ago

Kwai Tsing District, Hong Kong SAR 2 weeks ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.