Engineer, Equipment Validation; Medical Device MNC - Changi UP #HYT
Job in
Orchard, Antelope County, Nebraska, 68764, USA
Listed on 2026-03-01
Listing for:
Consortium for Clinical Research and Innovation Singapore
Contract
position Listed on 2026-03-01
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Biomedical Engineer, Quality Engineering
Job Description & How to Apply Below
Location: Orchard
Sector
Medical Devices / Pharmaceutical Manufacturing
LocationChangi
Employment Type9-Month Contract
Working HoursMonday to Friday
8:00 AM – 5:00 PM
The Engineer, Equipment Validation provides technical support for commercialization and manufacturing activities within a regulated sterile production environment. The role supports new product introduction, equipment qualification, validation processes, and continuous improvement initiatives to ensure robust, compliant, and efficient manufacturing operations.
Key Responsibilities- Lead and support new product introductions, including process scale-up and technology transfer activities
- Execute equipment qualification activities (IQ/OQ/PQ) and support PPQ and validation documentation
- Design and perform process experiments to evaluate equipment and process changes
- Provide technical support for sterile manufacturing operations, ensuring control of CPPs, CQAs, and process capability
- Investigate deviations, product complaints, and adverse events, performing root cause analysis and implementing CAPA in compliance with GMP requirements
- Support change control, cleaning validation, continued process verification, and lifecycle management activities
- Participate in risk assessments and process safety management activities
- Contribute to continuous improvement initiatives to enhance site performance metrics
- Support internal and external audits and regulatory inspections
- Bachelor’s Degree in Chemical Engineering, Mechanical Engineering, Chemistry, Biological Sciences, Pharmaceutical Sciences, or related discipline
- Minimum 3–5 years of experience in process engineering within a regulated manufacturing environment
- Hands‑on experience in equipment validation and qualification (IQ/OQ/PQ)
- Experience in medical devices or pharmaceutical manufacturing industry preferred
- Prior line start‑up experience is required
All qualified applicants, please click “APPLY NOW”.
Or you may send in your resume to:
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Email:
Kimmy Low Yi Ting (Kim) | CEI Registration Number: R
Recruit Express Pte Ltd Company Reg. No. W | EA LICENCE Number: 99C4599
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