CSV Engineer / Senior CSV Engineer (Remote / Onsite ) Singapore

Advanced Manufacturing Tech Solutions

Singapore

Hybrid

SGD 60,000 - 120,000

Full time

8 days ago
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Job summary

AMTSOL, a leader in Life Science Manufacturing Technology, seeks CSV Engineers for onsite Singapore roles and senior remote positions on global projects. You will execute CSV lifecycle activities across MES, automation, lab and equipment systems, and contribute to IQ/OQ/PQ documentation.

Ideal candidates have 2–3 years CSV validation experience in pharma, familiarity with GMP/GAMP 5, and the ability to work remotely with minimal supervision.

Qualifications

  • 2–3 years CSV/validation in pharma or life sciences.
  • GMP, FDA 21 CFR Part 11, and GAMP 5 familiarity.
  • Experience with MES/automation or lab systems preferred.

Responsibilities

  • Execute CSV lifecycle activities across MES, automation, lab and equipment.
  • Prepare IQ/OQ/PQ documentation and validation reports.
  • Develop and review validation protocols and test scripts.
  • Lead CSV/CQV initiatives for senior roles and manage changes.
  • Collaborate with QA, Engineering and Operations for compliance.
  • Mentor junior engineers and coordinate cross‑functional teams.
  • Apply e-validation tools like Kneat for paperless workflows.
  • Handle remote deliverables with minimal onsite supervision.

Skills

CSV validation
GMP awareness
Remote work

Education

Bachelor’s degree in Engineering/CS

Tools

Kneat
IQ/OQ/PQ docs

Job description

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)
About The Roles

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.
Requirements
CSV Engineer (Singapore - 2-3 Years)
  • 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.
Senior CSV Engineer (Remote - 6+ Years)
  • 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.
Lead/Senior CSV Engineer (Remote - 9+ Years)
  • 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.
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