[Hiring] GMP Equipment Validation Specialist @Akraya

Role Description

This role is responsible for ensuring GMP equipment remains validated and compliant through periodic reviews. You will collaborate with various departments to assess equipment performance, maintenance, and lifecycle. The position requires detailed documentation and analysis to maintain regulatory standards in a pharmaceutical setting.

Key Responsibilities:

• Conduct periodic reviews of GMP equipment.
• Evaluate equipment documentation and performance history.
• Prepare and revise review reports.
• Liaise with cross-functional teams to address equipment issues.
• Track and report on review progress and metrics.

Qualifications

• Commissioning/Qualification/Validation experience.
• GMP environment experience.
• Biotech/pharmaceutical manufacturing equipment knowledge.
• Experience in the pharmaceutical or biotech industry is required, with a focus on roles related to commissioning, qualification, and validation of manufacturing equipment.

Requirements

• Contract Type: W2 Contract.
• Duration: 12 Months.
• Location: #LI-Remote.
• Pay Range: $35.00 - $45.00 Per Hour.

Company Description

Akraya is an award-winning IT staffing firm consistently recognized for our commitment to excellence and a thriving work environment.

• Stevie Employer of the Year 2025.
• SIA Best Staffing Firm to work for 2025.
• Inc 5000 Best Workspaces in US (2025 & 2024).
• Glassdoor's Best Places to Work (2023 & 2022).

As a talent solutions provider for Fortune 100 Organizations, Akraya's industry recognitions solidify our leadership position in the IT staffing space.

Join Akraya Today! Let us lead you to your dream career and experience the Akraya difference. Browse our open positions and join our team!