Validation Engineer

Quanta Consultancy Services Ltd; New Jersey; On-site; USD 80,000 - 100,000; Full time

Job summary

Quanta Consultancy Services Ltd is seeking a Validation Engineer for a 6-month contract in New Jersey. This role is pivotal in supporting the qualification of equipment and processes in a pharmaceutical setting, ensuring compliance and efficiency in operations.

Ideal candidates will have extensive experience in Validation Engineering and possess strong organizational skills. Join us at the forefront of drug development and contribute to life-changing solutions for patients.

Qualifications

• Extensive experience as a Validation Engineer/Scientist.
• Ability to multitask and work independently.
• Strong organization and communication skills.

Responsibilities

• Generate and execute qualification documents (IQ/OQ/PQ protocols).
• Close out qualifications and generate summary reports.
• Support capital projects and process improvements.

Skills

Validation Engineering

Project Management

High Attention to Detail

Job description

Validation Engineer – US, New Jersey – 6 Month Contract

Ready to take your career to the next level with a global life sciences organization that’s shaping the future of drug development? We’re partnering with a pioneering pharmaceutical manufacturing company based in New Jersey to find driven, talented professionals who thrive in fast‑paced, high‑impact environments.

This is your opportunity to work at the cutting edge of science and manufacturing – collaborating with industry experts, contributing to breakthrough therapies, and playing a key role in delivering life‑changing solutions to patients worldwide. If you’re ambitious, detail‑oriented, and passionate about making a difference, this could be the role that defines your next chapter.

What You’ll Do

• Generate and execute qualification documents (IQ/OQ/PQ protocols) for equipment, facilities/HVAC, critical utilities, and contained charging processes for API manufacturing.
• Close out qualifications, generate summary reports, and resolve Veeva (Change Management System) action items.
• Support scheduled capital projects and plant/production support projects during the contract term, including corrective measure qualifications and process improvements.

What You’ll Need

• Extensive experience as a Validation Engineer/Scientist with a background in the project types outlined above.
• Ability to multitask and work independently with minimal assistance or guidance.
• Detail‑oriented with strong organization and communication skills.