Senior QC Equipment Validation Specialist

Amaris Consulting Pte Ltd

Singapore

On-site

SGD 60,000 - 90,000

Full time

3 days ago
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Benefits offered by this job

International community
Strong internal training
Vibrant workplace

Job summary

Amaris Consulting, Life Sciences division, is seeking a professional to support QC equipment qualification and decommissioning. You will define strategies and timelines, resolve equipment issues, and prepare qualification documents and training materials.

You will also contribute to method transfer and validation activities. Responsibilities include managing qualification in line with change-control and validation processes, decommissioning of QC equipment, and authoring SOPs and training

Qualifications

  • Fluent in English, both written and spoken.
  • Experience qualifying QC equipment and validating laboratory equipment.
  • Ability to author qualification documents and training materials.
  • Experience supporting deviations, CAPAs and change controls in lab equipment.
  • Experience coordinating decommissioning of QC equipment.

Responsibilities

  • Manage QC equipment qualification in line with change-control and validation processes.
  • Oversee decommissioning of QC equipment.
  • Define project strategies and timelines for qualification projects.
  • Support deviations, CAPAs and change controls arising from lab equipment issues.
  • Author SOPs, qualification documents, and training materials.
  • Support method transfer and validation activities.
  • Review qualification documents as required.

Skills

English (Fluent)
Project planning
QC equipment qualification

Education

Diploma or Bachelor's in Life Sciences

Job description

Amaris Consulting, Life Sciences division, is seeking a professional to support QC equipment qualification and decommissioning. You will define strategies and timelines, resolve equipment issues, and prepare qualification documents and training materials.

You will also contribute to method transfer and validation activities. Responsibilities include managing qualification in line with change-control and validation processes, decommissioning of QC equipment, and authoring SOPs and training

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