CSV Engineer/Senior CSV Engineer; Remote/Onsite
Remote / Online - Candidates ideally in
Singapore, Singapore
Listed on 2026-09-17
Singapore, Singapore
Listing for:
Advanced Manufacturing Tech Solutions
Remote/Work from Home
position Listed on 2026-09-17
Job specializations:
-
Engineering
Validation Engineer, Quality Engineering, Pharma Engineer, Biomedical Engineer
Job Description & How to Apply Below
AMTSOL:
A leader in Life Science Manufacturing Technology solutions, we are looking for top talent to be part of the dynamic team and drive the growth of the business.
AMTSOL:
A leader in Life Science Manufacturing Technology solutions, we are looking for top talent to be part of the dynamic team and drive the growth of the business.
Job Titles- CSV Engineer (Onsite, Singapore - 2-3 Years Experience)
- Senior CSV Engineer (Remote - 6+ Years Experience)
- Lead/Senior CSV Engineer (Remote - 9+ Years Experience)
The Role s
We are hiring CSV Engineers at multiple levels to support validation activities in GMP-regulated pharmaceutical environments. Opportunities are available for onsite engineers in Singapore and senior professionals working remotely on global projects.
Key Responsibilities- Execute Computerized System Validation (CSV) lifecycle activities across MES, automation, lab, and equipment systems.
- Perform Equipment Qualification (IQ/OQ/PQ) and system validation documentation.
- Author, review, and approve validation protocols, test scripts, and compliance reports.
- Lead and manage CSV/CQV strategy for senior roles, including deviation/change control.
- Collaborate with QA, Engineering, and Operations teams to ensure GMP and regulatory compliance.
- Mentor junior engineers and manage cross-functional validation teams (senior/lead levels).
- Utilize e-validation tools (e.g., Kneat) for paperless validation workflows.
- Remote roles:
Independently manage deliverables, deadlines, and stakeholder communication without direct onsite supervision.
- Bachelor’s degree in Engineering, Computer Science, or related discipline.
- 2-3 years of CSV/validation experience in pharma or life sciences.
- Familiarity with GMP, FDA 21 CFR Part 11, and GAMP 5.
- Exposure to MES validation, automation systems, or lab systems preferred.
- Bachelor’s/Master’s degree in Engineering, Computer Science, or related discipline.
- 6+ years CSV experience in pharma/life sciences.
- Strong knowledge of GMP, GAMP 5, and global compliance frameworks.
- Proven expertise in MES validation, automation validation, lab system validation, and equipment qualification.
- Ability to work remotely with minimal supervision.
- Bachelor’s/Master’s degree in Engineering, Computer Science, or related discipline.
- 9+ years CSV experience with leadership responsibilities.
- Demonstrated success in managing validation teams and complex global projects.
- Excellent stakeholder management, documentation, and leadership skills.
- Strong self-management and accountability in remote settings.
Position Requirements
10+ Years
work experience
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