Validation Engineer – Computer Systems & GMP Compliance

Medial Group; Villalba (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

Medial Group in Villalba, Puerto Rico, is seeking a Validation Engineer with 3+ years of experience in Process and Computerized Systems Validation. The role requires a Bachelor’s degree in Engineering and a background in FDA-regulated industries such as medical devices or biotech.

You will validate systems, develop IQ documentation, and ensure compliance with SDLC processes while collaborating with process owners and mentoring junior staff.

Qualifications

• Minimum 3 years of relevant validation experience with a Bachelor’s degree in Engineering.
• Hands-on experience in Process and Computerized Systems Validation.
• Background in FDA-regulated industries (medical devices, pharmaceuticals, biotech).
• Experience in medical devices or other highly regulated industry.
• Familiarity with SDLC processes.
• Experience configuring and troubleshooting Windows 10 desktops.
• Ability to work independently on moderately complex projects and mentor junior team members when needed.

Responsibilities

• Evaluate the impact of validated computerized systems on existing work instructions and processes.
• Prepare and execute computer system validation protocols and generate comprehensive reports.
• Develop and maintain Installation Qualification (IQ) documentation.
• Collaborate with process owners to implement changes to work instructions and ensure compliance.
• Inspect machinery, equipment, and tools to verify performance and initiate corrective actions as needed.
• Ensure adherence to company procedures, quality system regulations, and industry standards.
• Apply technical expertise and knowledge of engineering practices to optimize equipment and manufacturing techniques.
• Organize and track project progress, maintaining detailed documentation and status updates.
• Contribute to cross-functional projects and support milestone completion.
• Communicate effectively with internal stakeholders to share updates, gather input, and support decision‑making.
• Other duties may be assigned.

Skills

Bilingual English/Spanish

Root cause analysis

Technical writing

Strong communication

Process validation

Education

Bachelor's degree in Engineering

Tools

Windows 10

Job description

Medial Group in Villalba, Puerto Rico, is seeking a Validation Engineer with 3+ years of experience in Process and Computerized Systems Validation. The role requires a Bachelor’s degree in Engineering and a background in FDA-regulated industries such as medical devices or biotech.

You will validate systems, develop IQ documentation, and ensure compliance with SDLC processes while collaborating with process owners and mentoring junior staff.