Quality Engineer (validation)

Abbott

Singapore, Singapore
Not specified; range may vary by location
Execute validation protocols and documentation
Lead failure mode effects analysis (fmea)
Manage site validation review processes
The primary purpose of this role is to ensure that change control and validation activities are executed in a timely manner

Job Summary

  • The primary purpose of this role is to ensure that change control and validation activities are executed in a timely manner.
  • The incumbent will lead Failure Mode Effects Analysis (FMEA) for new equipment installations and manage site Validation Review processes.
  • Candidates must possess knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) within the pharmaceutical industry.

Matching Summary

The primary purpose of this role is to ensure that change control and validation activities are executed in a timely manner.

Salary

Not specified; Range may vary by location

Skills & Requirements

Must-have

  • Execute validation protocols and documentation
  • Lead Failure Mode Effects Analysis (FMEA)
  • Manage site Validation Review processes
  • Perform root cause analysis for quality events
  • Knowledge of GMP and GDP standards

Nice-to-have

  • Experience with Minitab or JMP data analysis
  • Familiarity with ISO and FSSC international standards
  • Background in manufacturing process design
  • Strong written English communication skills
  • Participation in internal and external audits

Key Requirements

  • Degree in Science or Engineering discipline
  • Minimum 3 years experience with Diploma in Science/Engineering
  • Proficiency in Microsoft Office applications

Work Rights

Not specified

Tailored Resume

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