
Validation Engineer
1 week ago
Support equipment, facilities, utilities qualifications
- Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and complete execution in a timely fashion
- Manage qualification execution and lead qualification deviation investigations encountered during qualification
- Collaborate with multi functions to arrange, plan and ensure smooth running of the qualification activities
- Participate in site Validation Maintenance Program
- Support Change Implementation on site
- Any other tasks as and when assigned by supervisor / Manager Support other technical changes and duties as required
**About You**
- Engineering/Science Degree or higher from recognised institution
- At least 2 years of experience in Equipment Qualification in the pharmaceutical/biotech industry.
- Experience in Critical Utilities, process equipment and facilities qualification is preferred.
- Good knowledge and experience of the practical and theoretical requirement of validation program in GMP facility
- Good Knowledge of Upstream, Downstream and Support Services equipment within the Pharma Biotech Industry.
- Good oral and written communication skills.
- Meticulous and Systematic
- Team player, with strong focus on safety, quality and timeline
- GMP/cGMP knowledge a plus
- Self-motivated and capable of working in diverse team situations with company clients and maintaining a positive attitude towards project challenges.
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