Job Description

The candidate is responsible to support equipment qualification, system qualification and cleaning validation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements.

Responsibilities:

• Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion.

• Manage qualification execution and lead validation deviation investigation encountered in qualification.

• Collaborate with multi functions to arrange, plan and ensure smooth running of the qualification activities

• Participate in site Validation Maintenance Program.

• Write execution related deviations and change requests.

• Support change implementation on site.

• Any other task as assigned by Supervisor/Manager
  

About You:

• Diploma / Bachelor Degree in Engineering / Science or related Pharmaceutical courses.

• Min. 2 years' experience in Equipment Qualification in the pharmaceutical/biotech industry. Experience in Critical Utilities, Cleaning validation and temperature mapping is preferred.

• Fresh Graduates welcome to apply.

• Good knowledge and experience of the practical and theoretical requirement of validation program in GMP facility.

• Good oral and written communication skills

• Meticulous and Systematic

• Team player, with strong focus on safety, quality, and timeline
  

Only shortlisted candidate will be notified. Contract length: 12 months Job Types: Full-time, Contract All staff to observe MOH regulations and practices.