Validation Expert for Pharmaceutical Facilities
1 day ago
The Senior Commissioning and Qualification Validation Engineer will create detailed documentation to support the commissioning, qualification, and validation of pharmaceutical facilities, utilities, and equipment.
Key Responsibilities include:
- Developing protocols for field verification and developing summary reports at client sites
- Planning and coordinating work and directing small teams in document development and/or execution
- Providing cGMP leadership and guidance for the integration and delivery of CQV services for life sciences clients
Required Skills and Qualifications:
- BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience
- 5-12 years' experience performing commissioning and/or qualification activities in an FDA-regulated industry
- Excellent technical problem-solving and troubleshooting skills, with solid knowledge of typical project technical issues
- High attention to detail and ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines
- Ability to work independently while quickly building and nurturing a project team
Benefits:
This is a mid-senior level full-time position requiring excellent communication and interpersonal skills.
We are seeking a skilled professional who can thrive in a dynamic environment and deliver high-quality results.
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