Validation and Compliance Engineer

ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients' needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.

Overview :

The Validation & Compliance Specialist will support the execution and maintenance of validation, quality, and compliance deliverables across facility, utility, equipment, and computerized systems. This role ensures that documentation and activities meet regulatory expectations and internal quality standards while supporting CAPA commitments and ongoing site validation programs.

Key Responsibilities :

1. Validation and Documentation Support

• Author, review, and update controlled documents including validation plans, protocols, reports, and procedures.
• Ensure all documentation aligns with current GMP standards and internal quality requirements.
• Maintain lifecycle traceability for validation deliverables and support document archival activities.

2. Assessments and Periodic Reviews

3. Qualification and Testing Activities

4. CAPA, Deviation, and Change Control Execution

5. Reporting and Continuous Improvement

Qualifications :

Preferred / Nice to Have :

Benefits : What We Offer :

Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.