Research scientist
1 day ago
Join us for the world we are making, redefining biosolutions for current and future generations to come, transcending planetary boundaries, sustainability, and One Health.
GrowthWe empower each other to produce better results by providing professional advancement and personal growth.
We are driven by the challenge of creating something new and discovering better opportunities.
We value a positive attitude. We make working a more pleasant experience for everyone.
CommunicationWe value communication, for it creates better intercultural relationships.
CompetenceWe focus on things that matter most and help each other drive success.
CommitmentWe see the good. We work hard. We keep things in balance.
BENEFITSLearning and Development
Competitive Compensation
Overseas Travel Opportunities for many positions
One Team, One MissionAre you a seasoned professional looking for your next challenge? Be one of us
Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200 M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, and Oceania.
Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.
Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.
Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which we often use as the factory to derive our target product.
Our first commercial breakthrough success is Esco Aster being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.
We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full c GMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.
The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.
Join us as we redefine Bio Solutions for One World and One Health for the current and future generations to come.
One World Biosolutions for One Health.
Who we’re looking forAbility to read, analyze and interpret scientific data and publications.
Ability to author or review protocols, technical reports and technology transfer documents.
Ability to adapt and keep up with rapid changes in a fluid and dynamic environment as this is a rapidly evolving space.
Repetitive motions due to certain laboratory techniques.
Ability to define problems, collect data, establish facts, and draw conclusions.
Ability to author and review standard operating procedures, batch records, protocols, data, reports and other related documents.
Report To:Selected candidate will report to CEO and others as assigned.
The ScopeYou will be part of Esco Aster’s scientific division and contribute to the company’s CDMO mission and objectives. You will perform research and process development activities, in various projects and in collaboration with internal and external stakeholders, clients and partners.
Job ResponsibilitiesDesign and Independently Execute Experiments:
Design and laboratory-scale experiments to support client upstream processes and requests.
Perform assay development and data analysis.
Upstream Process Evaluation and Optimization:
Evaluate and optimize existing client processes in preparation for scale-up.
Propose improvements and modifications to enhance process efficiency.
Scale-Up and Technology Transfer:
Conduct scale-up experiments in larger bioreactors.
Adapt processes to align with available on-site equipment.
Facilitate technology transfer from clients, aiming at scaling up processes or implementing new technologies (e.g., perfusion, serum replacements).
Continuous Process Improvement:
Proactively identify opportunities for process improvements.
Initiate and drive enhancements to streamline processes.
Project Management and Documentation:
Write client proposals, outlining milestones, timelines, and budgets for scale-up projects.
Take ownership and accountability for all deliverables and milestones in assigned projects.
Summarize project work in a formal report and communicate effectively to stakeholders.
Cross-Functional Collaboration:
Collaborate across different teams to troubleshoot, test, and optimize various issues.
Work seamlessly in a cross-functional environment.
Subject Matter Expert Support:
Support sales, business development, product specialists, and associated departments as a subject matter expert.
Ad Hoc Tasks:
Undertake other tasks as assigned based on project needs.
Flexible Work Schedules:
Adapt work schedules as needed to accommodate cell culture schedules.
RequirementsMinimum Master’s degree in Biology or related science.
At least 1-2 years related laboratory experience in mammalian cell culture, stem cells, immunology or exosomes.
Experience with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) will be an advantage.
Proficient in MS Office Suite (Microsoft Word, Power Point, Excel).
Experience in isolation of stem cells, tissue banking and generation of cell bank.
Experience with cell assays such as FACS, ELISA, biological assays.
Experience with bioreactor systems.
General laboratory skills, good pipetting skills and experience with automation.
Strong computer, scientific, and organizational skills.
Excellent communication (oral and written) and attention to detail.
Strong team player, develop positive relationship with a strong set of interpersonal skills.
Ability to work independently and as part of a team, self-motivated, adaptable, and has a positive attitude.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
A friendly and pleasant disposition.
Interested candidates, please submit a Cover Letter and CV #J-18808-Ljbffr
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