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Job Title: Bioinformatics Manager
Location: Singapore
Mode of working: Full-time
About the Company:
Amoy Diagnostics Co., Ltd. (AmoyDx) is an R&D based diagnostic company, focusing on molecular diagnostics for oncology precision medicine. With completely independent intellectual property rights of ADx-ARMS®, Super-ARMS®, ddCapture® and ADx-HANDLE® technologies, AmoyDx has a market-leading portfolio of molecular diagnostic assays.
At AmoyDx, our mission is to improve healthcare and patients' lives with superior & innovative products and services. Our vision is to be one of the global leading and most reliable suppliers of quality diagnostic products and services for personalized healthcare.
Position Overview:
We are seeking a highly skilled and experienced Manager of Bioinformatics to lead our dynamic team of bioinformatics scientists and contribute to our mission of advancing healthcare through computational biology. The successful candidate will be responsible for driving the development and implementation of bioinformatics strategies, and collaborating cross-functionally with research, development, and clinical teams.
Key Responsibilities:
· Provide strategic direction and leadership for the bioinformatics team, fostering a culture of innovation, collaboration, and excellence.
· Mentor and develop team members, ensuring their professional growth and success.
· Oversee recruitment, onboarding, and performance management processes for the bioinformatics team.
· Develop and implement bioinformatics strategies to support drug discovery, development, and clinical research programs.
· Collaborate with research and development teams to identify and prioritize bioinformatics needs and opportunities.
· Stay abreast of emerging trends, technologies, and methodologies in bioinformatics and computational biology.
· Lead the analysis and interpretation of genomic, transcriptomic, proteomic, and other omics data sets to support research and development projects.
· Apply statistical and computational methods to extract meaningful insights from complex biological data.
· Work closely with biologists, chemists, and clinicians to translate bioinformatics findings into actionable recommendations.
· Foster collaboration and communication between bioinformatics, research, development, and clinical teams.
· Present bioinformatics findings, methodologies, and strategies to internal stakeholders and external partners.
· Contribute to scientific publications, presentations, and grant proposals.
· Ensure compliance with regulatory requirements and industry standards for data management, analysis, and reporting.
· Implement best practices for data quality control, reproducibility, and documentation.
· Collaborate with IT and informatics teams to optimize bioinformatics infrastructure and workflows.
Qualifications:
· Masters, Ph.D. or equivalent experience in bioinformatics, computational biology, or a related field.
· Minimum of 5 years of experience in bioinformatics or computational biology in the pharmaceutical, biotechnology, or academic research setting.
· Strong expertise in bioinformatics tools, algorithms, and databases for the analysis of genomic, transcriptomic, and proteomic data.
· Proficiency in programming languages such as Python, R, or Perl, and experience with bioinformatics software packages and pipelines.
· Excellent analytical, problem-solving, and critical-thinking skills.
· Effective communication and interpersonal skills, with the ability to collaborate across multidisciplinary teams.
· Familiarity with regulatory requirements and quality standards for bioinformatics in the pharmaceutical or biotechnology industry is desirable.
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Job Title: R&D Senior Director
Location: Singapore
Mode of working: Full time
About the Company:
Amoy Diagnostics Co., Ltd. (AmoyDx) is an R&D based in-vitro diagnostic company, focusing on molecular diagnostics for oncology precision medicine. With completely independent intellectual property rights of ADx-ARMS®, Super-ARMS®, ddCapture® and ADx-HANDLE® technologies, AmoyDx has a market-leading portfolio of molecular diagnostic assays.
At AmoyDx, our mission is to improve healthcare and patients' lives with superior & innovative products and services. Our vision is to be one of the global leading and most reliable suppliers of quality diagnostic products and services for personalized healthcare.
Job summary:
We are hiring a Research and Development Senior Director to lead the strategic vision and execution of research and development initiatives within the organization. You will be responsible for overseeing all aspects of the R&D process, including project management, team leadership, resource allocation, and innovation strategy. Your role is pivotal in driving technological advancements, product development, and market competitiveness.
Key Responsibilities:
· Strategic Planning: Develop and execute the R&D roadmap aligned with the company's objectives and market trends. Identify opportunities for innovation and technological advancement to maintain a competitive edge.
· Team Leadership: Lead, mentor, and motivate a team of researchers, scientists, engineers, and technicians. Foster a collaborative and innovative culture conducive to creativity and high-performance.
· Project Management: Oversee multiple R&D projects from inception to completion. Define project goals, timelines, and milestones. Ensure projects are executed within budget and meet quality standards.
· Resource Allocation: Manage budgetary allocations for R&D activities. Optimize resource utilization and prioritize projects based on strategic importance and potential impact.
· Cross-Functional Collaboration: Collaborate with other departments such as product management, marketing, and manufacturing to ensure alignment between R&D efforts and business objectives. Foster strong interdisciplinary relationships to facilitate seamless integration of new technologies and products.
· Technology Assessment: Stay abreast of emerging technologies, industry trends, and competitive landscapes. Evaluate new technologies for their applicability and potential to drive innovation within the organization.
· Regulatory Compliance: Ensure that all R&D activities comply with regulatory standards and industry best practices. Work closely with regulatory affairs teams to navigate regulatory requirements and obtain necessary approvals.
· Intellectual Property Management: Oversee the development and protection of intellectual property assets generated through R&D activities. Manage patent portfolios and intellectual property strategies to safeguard the organization's innovations.
· Performance Monitoring and Reporting: Establish key performance indicators (KPIs) to measure the effectiveness of R&D initiatives. Provide regular reports and updates to senior management on project progress, budgetary status, and strategic achievements.
· Continuous Improvement: Drive a culture of continuous improvement within the R&D organization. Identify areas for optimization, process refinement, and efficiency enhancement.
Qualifications:
· Advanced degree (Ph.D. preferred) in a relevant scientific discipline.
· Proven track record of leadership in research and development, preferably in a managerial capacity.
· Extensive experience in project management, resource allocation, and budgetary oversight within the oncology diagnostics field.
· Strong understanding of R&D processes, methodologies, and best practices.
· Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.
· Strategic thinker with a forward-looking vision and the ability to anticipate market trends and technological advancements.
· Demonstrated ability to drive innovation and bring products from concept to commercialization.
· Knowledge of regulatory requirements and intellectual property management.
· Results-oriented mindset with a focus on delivering high-quality outcomes and achieving business objectives.
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We’re hiring an APAC Medical Affairs Manager to join us, who will play a critical role in bridging the gap between the APAC medical and commercial aspects in AmoyDx.
Job responsibilities:
· Medical Strategy Development:
o Develop and implement medical affairs strategies in alignment with overall business goals.
o Provide input into the development of medical plans, ensuring integration with marketing and sales strategies.
· Scientific Communication:
o Serve as a key point of contact for scientific and medical information within the organization.
o Develop and review scientific content for medical communications, educational materials, and promotional activities.
· Pharma partners and KOL Engagement:
o Identify and engage with pharma partners, Key Opinion Leaders (KOLs) and other stakeholders to foster relationships and gather insights.
o Collaborate with KOLs to support educational initiatives, advisory boards, and research collaborations.
· Regulatory Support:
o Work closely with the regulatory affairs team to ensure compliance with relevant regulations and guidelines.
o Support the preparation of regulatory submissions by providing scientific and medical input.
· Clinical Support:
o Provide medical input into the development of clinical trial protocols and study designs.
o Collaborate with clinical operations to ensure the successful execution of clinical trials.
· Training and Education:
o Develop and deliver training programs for internal stakeholders, including sales teams and customer support.
o Stay informed about advancements in medical science and ensure the organization's teams are educated on relevant topics.
· Collaboration with Cross-Functional Teams:
o Work collaboratively with marketing, sales, market access, and other departments to ensure consistent messaging and alignment of activities.
· Data Analysis:
o Analyze and interpret scientific and clinical data to inform decision-making and support product positioning.
· Budget Management:
o Manage the medical affairs budget, ensuring efficient use of resources and adherence to financial guidelines.
· Compliance:
o Ensure that all medical affairs activities adhere to relevant compliance standards, industry codes, and regulations.
Requirement:
· Medical degree
· Experience working with pharmaceutical industry is highly preferred.
· Minimum of 5 - 7 years of experience in medical affairs
· Strong understanding of medical and scientific principles, as well as regulatory requirements.
· Excellent communication and presentation skills.
· Ability to work collaboratively in cross-functional teams.
· Strong project management and organizational skills
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