QA Validation Engineer

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QA Validation Engineer (USP)

ND Reference : JDSG201703.044.01QAE

Position available with No Deviation Pte. Ltd. supporting a MNC Client in the pharmaceutical industry

General Description

Quality Assurance Personnel with pharmaceutical background and experience in Validation required to apply expertise in the systematic and detailed review of Equipment Qualification and CSV documentation, Turnover documentation, and Operational Procedures.

Must have strong knowledge and understanding of validation life-cycle and apply both site quality requirements and standard GMP requirements.

Education / Licenses:

  • Degree in Engineering, Science or related technological field
  • At least 5 – 7 years’ experience in equipment validation within the pharmaceutical industry

 

Competencies / Skills:

  • Ability to interpret and operate within defined schedules managing available resources to achieve project milestones
  • Proactive, self-starter and capable of working alone or in a team environment
  • Comprehensive understanding of commissioning, qualification and verification requirements
  • Good knowledge of cGMP, GDP and ICH Q10 and ASTM E2500 risk-based approaches
  • Support updating document trackers to monitor status of all documents
  • To be aware and supportive of the project’s requirement for flexibility in working hours/shift patterns through the differing phases of the project’s life cycle
  • Good communication skills (technical writing and verbal communication/presentation)
  • Interacts effectively with variety of communication and working styles
  • Able to provide internal validation training if required
  • Be IT literate and familiar with Microsoft office suite of applications
  • Proven track record in following and promoting Safety in all aspects of your role
All applications will be held in the strictest confidence with no information shared externally without prior consent.

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