Validation Engineer

ESCO ASTER PTE. LTD.; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading life sciences company in Singapore is seeking a candidate to join their MSAT team, focusing on commissioning, qualification, and validation activities within a GxP environment. The ideal applicant will have a degree in Engineering or Science and experience in the pharmaceutical sector. This role involves working closely with cross-functional teams to ensure compliance and operational excellence while fostering a culture of continuous improvement. Interested candidates should submit a Cover Letter and CV to the provided email address.

Qualifications

• Minimum of 1-3 years’ experience in pharmaceutical/biopharmaceutical manufacturing.
• Familiarity with GxP standards and regulatory requirements.
• Ability to work independently and communicate effectively.

Responsibilities

• Perform risk-based commissioning, qualification, and validation.
• Develop validation protocols and reports.
• Coordinate with internal teams to achieve CQV objectives.

Skills

Risk management

Technical writing

Communication

Team collaboration

Education

Degree in Engineering or Science

Tools

MS Office Suite

Job description

The Opportunity

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, 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 often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class 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 cGMP 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.

The Scope

You will be part of Esco Aster's MSAT team and contribute to the overall site mission and objectives. You will ensure Commissioning Qualification and Validation (CQV) activities and tasks are planned and executed in an efficient and compliant manner, while adhering to GxP standards. You will work with the Leadership team of MSAT to develop a continuous improvement mindset and engage in teamwork with cross-functional departments.

Primary work location: Ayer Rajah Crescent, Singapore

Job Responsibilities

• Perform risk-based commissioning, qualification and validation of pharmaceutical and biopharmaceutical equipment, utilities, facilities and processes.
• Develop validation protocols and reports that fulfil regulatory requirements and industry best practices.
• Assist in developing User Requirements Specification documents.
• Prepare design review and design qualification documents at the initial design stage to align with specifications.
• Generate protocols and execute field work related to Commissioning (FAT, SAT), Installation & Operational Qualification (IOQ).
• Prepare and execute FMEA and validation activities pertaining to Performance Qualification (PQ), Computerized System Validation (CSV), Cleaning Validation, Thermal Validation and Transport Qualification, as required.
• Complete assigned CQV tasks according to planned schedule, budget, safety and engineering standards.
• Coordinate with internal teams (manufacturing, engineering, quality etc.) to achieve CQV objectives.
• Coordinate and manage external parties, primarily vendors and contractors to achieve CQV objectives.
• Investigate deviations and write deviation reports and findings.
• Support Engineering and Facilities functions as needed.
• Undertake tasks assigned by leaders as and when appropriate.

Requirements

• Degree and/or Diploma in Engineering/Science or related studies.
• Minimum of 1-3 years’ experience in pharmaceutical/biopharmaceutical manufacturing facility.
• Familiar with working in a GxP environment and keeping up to date with current GxP, with flexibility to change as needed due to new regulatory requirements and technologies, as relevant for clinical and commercial supply.
• Good knowledge of GxP, GDP, CQV approaches including Validation Lifecycle approach (URS, DQ, FAT/SAT, IOQ, CSV, Cleaning/ Thermal Validation etc.), regulatory requirements and best industry practices.
• Competent in technical writing and presentations.
• Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
• Able to work independently, self-starter, self-motivated and task oriented.
• Good communication skills and able to openly communicate and escalation of any relevant issues.
• Strong team player to work with both internal and external stakeholders.
• Develop positive relationship with a strong set of interpersonal skills.
• Prepared to travel and reside abroad to ensure the successful execution of external projects, if required.

Interested candidates, please submit a Cover Letter and CV to [e-mail].