Job Description

EQUIPMENT VALIDATION

Lincoln, RI

Long term Contract

An Equipment Validation Specialist in the pharmaceutical industry plays a crucial role in ensuring that all equipment used in the production process is functioning correctly and meets regulatory requirements. Here are some key responsibilities and duties for this role:

Responsibilities

• Develop and execute validation protocols for various types of equipment.
• Perform equipment inspections and testing to ensure compliance with regulatory standards.
• Prepare and review validation documentation , including validation plans, reports, and standard operating procedures.
• Coordinate with engineering, quality assurance, and production teams to resolve equipment-related issues.
• Monitor equipment performance and implement corrective actions as needed.
• Maintain up-to-date knowledge of industry regulations and standards related to equipment validation.
• Conduct training sessions for staff on proper equipment usage and validation procedures.
• Participate in internal and external audits related to equipment validation.

Qualifications

• Bachelor's degree in engineering, life sciences, or a related field .
• Strong understanding of validation protocols and regulatory requirements .
• Excellent problem-solving abilities and attention to detail.
• Effective communication and teamwork skills .

Thanks

Ritika Aithmian

Lead Recruiter

D : +1 617-848-2313 (P)

Ritika.aithmian@mastechdigital.com

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