About the Role
Are you detail-oriented and skilled in documentation and reporting?
Join our team as an Assistant Validation Engineer, where you'll play a key role in supporting the development and qualification of automated assembly machines for the medical and pharmaceutical industry.
This is an ideal opportunity for someone who enjoys working with technical teams and wants to grow in a regulated, high-impact environment.
You'll work closely with engineers and receive on-the-job training from a dynamic and experienced manager.
What You'll Do:
- Collaborate with engineers to draft technical documentation that explains the function and operation of assembly machines.
- Prepare and maintain validation documents in accordance with GMP, regulatory standards, and Mikron internal procedures.
- Support the creation and execution of Factory Acceptance Test (FAT) and Site Acceptance Test (SAT).
- Ensure documentation is clear, accurate, and audit ready.
- Assist the Validation team in delivering projects on time and with high quality.
- Take on additional tasks as assigned by management.
What We're Looking For:
- Bachelor's degree/diploma in Mechanical engineering or equivalent
- Strong technical writing and documentation skills
- Ability to understand and describe mechanical and automation systems
- A proactive learner with a keen eye for detail
- Team player who can work closely with engineers and project teams
- Familiarity with validation or regulated environments is a plus—but not required
- SINGAPOREAN /PRS ONLY.
We regret that only shortlisted candidates will be notified.
Thank you for applying.