Careers with Invitrocue

Why Invitrocue? Join a game-changing company where you’ll gain exposure and work in a dynamic environment to over-deliver and outperform. A career with Invitrocue means your everyday work improves patients’ lives around the world.

Open Positions

Invitrocue is a bioanalytics company that develops predictive human in vitro cell based and humanized models that enable the pharmaceutical and biotechnology industry to reduce risk, reduce cost and shorten time to market. Invitrocue’s cell-based assay systems and humanized animal models are useful for preclinical drug discovery and efficacy screening.  Invitrocue’s Onco-PDO Phenotype-driven Precision Oncology technology platform, helps to predict treatment response using autologous Patient Derived Organoids/Cell lines.  Invitrocue’s technologies originated from Singapore’s Agency for Science, Technology and Research (A*STAR).

Why Invitrocue?  Join a game-changing company where you’ll gain exposure and work in a dynamic environment to over-deliver and outperform.  A career with Invitrocue means your everyday work improves patients’ lives around the world. 

Summary:

A Project Manager is required to drive multiple projects encompassing clinical validation studies for Onco-PDO, product registrations and project management for Consumables business unit. This position will report to General Manager, Singapore.

Essential Functions:

1. Manages projects from proposal development to final deliverables. Based out Singapore, managing projects in South-East Asia across various phases and functional areas.
2. Project Administration: Acts as primary liaison to ensure project / clinical study organization, launch, conduct / implementation, management and closeout. Establish and maintain good rapport and professional working relationship with all collaborators for clinical studies, vendors and suppliers for products in Consumables business.
3. Financial Aspects: Prepare budgets, track and report on expenses and project financial status. Coordinate with Finance on invoicing to customers.
4. Project Planning: Develops and maintains project plans in accordance with Standard Operating Procedures (SOPs) and Work Instructions (WI).
5. Project Tracking: Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools. Produces and distributes status, resourcing, and tracking reports to appropriate team members and senior management. Alerts senior management to potential issues and ensures necessary corrective and preventive actions are taken.
6. Regulatory Affairs: Be proficient with relevant regulatory guidelines, stay updated and provide regulatory consultation to internal project teams to ensure compliance. Ensure project documentation are complete and audit-ready. Oversee regulatory documents collection and submission process.

Other Responsibilities:
May represent company at professional meetings, seminars or conferences. Performs other work-related duties as assigned.


Requirements:
1. Bachelor’s or Master’s degree in Life Science, Pharmacy or Business, or equivalent combination of education and experience.
2. > 2 years technical or managerial experience in project management.
3. Working knowledge in Singapore regulations (e.g. Human Biomedical Research Act, Medical Device registration etc) and/or other regional regulations for in-vitro diagnostics or medical devices would be preferred.
4. Strong written, presentation, documentation, and interpersonal skills as well as a team-oriented approach.
5. Proficient computer skills in Word, Excel, PowerPoint, and Internet.
6. Basic computer skills using MS Project.
7. Ability and flexibility to work under pressure, handle multiple tasks to meet deadlines and deliver high quality work in a dynamic environment.
8. Methodological, resourceful and possess problem-solving skills.
9. Highly driven & self-motivated.
10. Ability to work independently with minimal supervision and as part of a team.
11. Strong attention to detail and ability to multi-task projects, priorities, schedules, and deliverables.

Interested candidates, please submit a CV to contact@invitrocue.com. We regret to inform that only shortlisted candidates will be notified.

Invitrocue is a bioanalytics company that develops predictive human in vitro cell based and humanized models that enable the pharmaceutical and biotechnology industry to reduce risk, reduce cost and shorten time to market. Invitrocue’s cell-based assay systems and humanized animal models are useful for preclinical drug discovery and efficacy screening.  Invitrocue’s Onco-PDO Phenotype-driven Precision Oncology technology platform, helps to predict treatment response using autologous Patient Derived Organoids/Cell lines.  Invitrocue’s technologies originated from Singapore’s Agency for Science, Technology and Research (A*STAR).

Why Invitrocue?  Join a game-changing company where you’ll gain exposure and work in a dynamic environment to over-deliver and outperform.  A career with Invitrocue means your everyday work improves patients’ lives around the world. 

Summary:

A Quality Management Manager is required to lead and drive compliance to all quality processes and procedures developed for in-vitro and in-vivo preclinical services and products, clinical services and consumables business units.  This position will report to General Manager, Singapore

Essential Functions:

1. Be responsible for the establishment and maintenance of a quality management system for in-vitro and in-vivo preclinical services and products, and Onco-PDO clinical services business unit.
2. Set requirements for all products and service assays based on prevailing industry standards and regulations, and monitor for compliance.
3. Initiate the development of specific quality procedures and SOP’s by engaging Process Owners and internal Approvers. Maintain full sets of quality procedures and SOP’s and implement regular updates to these documents.
4. Develop internal quality management tools to regularly assess all product and assay development procedures to identify deviations from quality standards and implement corrective action plans.
5. Assess the product’s and service’s quality by testing for a range of features.
6. Investigate causes of quality problems, propose solutions and engage all key stakeholders in implementation.
7. Take appropriate actions in championing and developing the culture of quality improvement and awareness.
8. Initiate and implement improvements to production processes that lead to overall increases in product and service quality, and process efficiency.
9. Work together with Department Heads and Project Leaders to discuss solutions to quality issues.
10. Create production plans for new products to guarantee quality from stage one.
11. Solicit feedback from customers to assess whether their requirements are met.
12. Plan, develop and support the training of employees in Quality Management and Quality Control processes and procedures.
13. Provide continuous education on newly developed Quality Control techniques.
14. Act as liaison person for any external audits or inspections by regulatory authorities or
Clients. Lead the audit process from preparation, attendance, follow up to close-out.
15. Provide report of Quality Management activities and performance.

Other Responsibilities:
May represent company at professional meetings, seminars or conferences. Performs other work-related duties as assigned.


Requirements:
1. Bachelor’s or Master’s degree in Life Science/Pharmacy, or equivalent combination of education and experience.
2. At least 3 year’s experience in a quality management, QA/QC role within pharma or life sciences related industry.
3. Experience in devising and establishing a company’s quality procedures, standards and specifications.
4. Good knowledge of quality management standards and production management (e.g. ISO 15189 / 13485, GCP, GMP, GLP).
5. Hands on experience liaising with the HSA/MOH/US FDA etc and various other regulators preferred.
3. Working knowledge in Singapore regulations (e.g. Human Biomedical Research Act, Medical Device registration etc) and/or other regional regulations for in-vitro
diagnostics or medical devices would be preferred.
4. Strong written, presentation, documentation, and interpersonal skills as well as a team-oriented approach.
5. Proficient computer skills in Word, Excel, PowerPoint, and Internet.
6. Basic computer skills using MS Project.
7. Ability and flexibility to work under pressure, handle multiple tasks to meet deadlines and deliver high quality work in a dynamic environment.
8. Methodological, resourceful and possess problem-solving skills.
9. Highly driven & self-motivated.
10. Ability to work independently with minimal supervision and as part of a team.
11. Strong attention to detail and ability to multi-task projects, priorities, schedules, and deliverables.

Interested candidates, please submit a CV to contact@invitrocue.com. We regret to inform that only shortlisted candidates will be notified.

Contact with Invitrocue

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