Sr. Validation Engineer

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Must be legally authorized to work in the United States without sponsorship**

Who Youll Work With

You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work directly with our clients. You will be welcomed into a rapidly growing business and team, empowered to make an impact, and supported in your growth as a professional. You will work with industry experts in our Regulatory Compliance Practice, delivering high-quality solutions to clients.

What Youll Do

You will support capital projects and implement solutions for clients, helping them improve performance and achieve goals. Responsibilities include:

Preparing, executing commissioning and qualification documents for utility, facility, and process equipment.

Developing and executing validation and FDA compliance documents/protocols for pharmaceutical equipment.

Making an impact through your skills and expertise, strengthening client and team relationships.

What Youll Bring

Minimum 5 years of experience in validation of pharmaceutical or medical device processes and equipment.

Experience with FAT, SAT, IQ, OQ documentation on Automated Systems in Pharma.

Validation experience in automation, packaging, cleaning, computer systems, utilities, or facilities is desired.

Strong leadership, organization, communication, and interpersonal skills.

Proficiency in computer skills.

Willingness to travel as needed for project activities.

Bachelors degree in Electrical, Mechanical, Chemical Engineering, or related field.

Our culture values mutual respect, integrity, and professional growth. We support your development through mentorship, training, and career planning. Join us to build a meaningful career surrounded by talented professionals and leaders committed to your success. #J-18808-Ljbffr