Work alongside Sr. Project Associate throughout project phases and clinical trials including initiation, design, execution, and completion of research projects.
Collaborate with Sr. Project Associate in developing and managing project plans, schedules, and budgets.
Assist expenses monitoring of each Research and Development team to ensure alignment with other departments.
Manage and maintain the organization and neatness of the Research and Development archive, ensuring proper foldering, version control, and easy accessibility of project documentation.
Co-manage reimbursable invoices reconciliation process and purchase requests.
Engage and collaborate with relevant departments to facilitate the effective and efficient completion of Research and Development projects.
Promote a culture of continuous improvement and innovation within the project team, including contributing creative ideas and supporting the development of product packaging.
Bachelor’s degree Life Sciences, Industrial Engineering or a related field.
Minimum 1 year of relevant experience in Research and Development, project management, or a related field is preferred.
Familiarity with project management tools (e.g., Notion, Asana) is considered an advantage.
Strong leadership potential and a proactive attitude toward taking ownership of tasks.
Eagerness to learn and grow within a fast-paced environment.
Agile and adaptable mindset to manage shifting priorities and dynamic project needs.
Excellent communication and collaboration skills, with the ability to work effectively across departments.
Organized, with strong critical thinking and problem-solving abilities, and excellent attention to detail.
Lead and responsible for conducting Quality Control (QC) inspections on raw materials, packaging, and consumables used in production, as well as materials for research and laboratory use (chemicals, reagents, and consumables), following established procedures.
Lead and responsible for conducting in-process Quality Control (QC) based on established procedures and production schedules, and issuing Certificates of Analysis (CoA) when test results meet defined standards/specifications.
Perform library preparation, quality control, and sequencing runs using Illumina platforms (e.g., MiSeq, NextSeq, NovaSeq).
Conduct troubleshooting for any issue/problem that might arise during the testing and inspection activity.
Bachelor of Science in Biology, Pharmaceuticals, Chemistry, or other related major.
Minimum of 3 years of experience in QC and laboratory operations, with at least 2 years of experience in a supervisory or lead role.
Having experience at least 2 years of hands-on experience in laboratory/research roles, including NGS workflows in academic or industry settings.
Having experience in PCR, qPCR, electrophoresis, nucleic acid extraction, and NGS library preparation.
Having excellent pipetting skills.
Understanding of GMP, GLP, CPAKB, ISO 9001, ISO 13485, and ISO 17025 is an added value.
