
Senior Validation Engineer
1 week ago
**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 commission and qualification execution
- Support 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**:
- Bachelor Degree in Engineering/Science.
- Min. 3 to 5 years' experience in Equipment Qualification in the pharmaceutical/biotech industry. Experience in Critical Utilities, Cleaning validation and temperature mapping is preferred.
- 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
- Contract for 12 months. Subject to renewal.
**Notes**:
Contract length: 12 months
**Job Types**: Full-time, Contract
Contract length: 12 months
**Salary**: $4,000.00 - $4,500.00 per month
Schedule:
- Monday to Friday
COVID-19 considerations:
All staff to observe MOH regulations and practices
**Experience**:
- Pharma Industry: 3 years (preferred)
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