Lab Analytics & Validation Lead (18-Month Contract)

GMP Technologies

Singapore

Sur place

SGD 40 000 - 60 000

Plein temps

14 jours+

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Résumé du poste

UK Pharma in the West region is seeking an Analytical Support Officer for an 18-month contract. The role focuses on maintaining calibrated analytical equipment, leading investigations, and ensuring regulatory compliance in a GMP environment.

You will lead validation activities, manage change controls, train staff, and support internal audits while upholding quality and safety standards in a lab setting.

Qualifications

  • Min. Science degree holder with experience in Chemical, Pharma or Manufacturing industry.
  • Good knowledge of GMP and laboratory equipment/validation.
  • Good knowledge of quality, laboratory techniques and laboratory compliance.
  • Good knowledge of regulatory expectations /CAP/ICH requirements.

Responsabilités

  • Ensure analytical equipment are maintained and calibrated per site procedures and regulatory requirements.
  • Lead/participate in investigations from laboratory equipment/system events and propose CAPA.
  • Perform periodic validation review of systems/lab equipment and recommend re-validation.
  • Lead/participate in equipment validation and approve related documents.
  • Maintain and support computer systems and equipment per change control procedures.
  • Assess impact of changes on laboratory equipment and documentation.
  • Revise and maintain laboratory procedures to ensure compliance.
  • Ensure a safe lab environment and perform 6S inspections.
  • Supervise, develop and motivate staff; conduct training on systems/equipment.
  • Ensure regulatory compliance, perform audits.

Connaissances

GMP knowledge
Lab equipment validation
Quality systems

Formation

Science degree

Description du poste

UK Pharma in the West region is seeking an Analytical Support Officer for an 18-month contract. The role focuses on maintaining calibrated analytical equipment, leading investigations, and ensuring regulatory compliance in a GMP environment.

You will lead validation activities, manage change controls, train staff, and support internal audits while upholding quality and safety standards in a lab setting.

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