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Engineer, Equipment Validation; Medical Device MNC - Changi UP #HYT

Job in Orchard, Antelope County, Nebraska, 68764, USA
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
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Engineer, Equipment Validation (9-Month Contract) Medical Device MNC - Changi UP 7K #HYT
Location: Orchard

Sector

Medical Devices / Pharmaceutical Manufacturing

Location

Changi

Employment Type

9-Month Contract

Working Hours

Monday to Friday
8:00 AM – 5:00 PM

Job Summary

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
Requirements
  • 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:

Whatsapp: (Use the "Apply for this Job" box below)./

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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