Validation Engineer

BW Design Group; Boston (MA); On-site; USD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking a Validation Engineer II to join their dynamic team. This role involves collaborating with experts to solve complex challenges in the pharmaceutical sector, ensuring regulatory compliance and delivering high-quality solutions. You will be responsible for developing validation documents, troubleshooting issues, and supporting clients on-site. The company fosters a culture of respect and professional growth, encouraging diverse candidates to apply. If you are passionate about making an impact in the industry and growing your career, this opportunity is perfect for you.

Qualifications

• 3+ years of validation experience in automation, packaging, utilities, or facilities.
• Experience in pharmaceutical or biotech environments preferred.

Responsibilities

• Develop and execute validation and FDA compliance documents for pharmaceutical equipment.
• Travel to client sites for design, validation, and project support.

Skills

Strong communication skills

Validation experience

Technical writing skills

Proficiency with MS Office

Experience in pharmaceutical environments

Education

B.S. in Bioengineering

B.S. in Biomedical Engineering

B.S. in Chemical Engineering

Tools

AutoCAD

MS Project

Job description

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Who You’ll 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 clients on impactful projects. You will be valued, challenged, and supported to grow into a world-class professional.

Job Description

As a Validation Engineer II, you will collaborate with industry experts to solve complex problems for leading companies. You will support regulatory compliance and deliver high-quality solutions in the pharmaceutical industry.

What You’ll Do

• Develop and execute validation and FDA compliance documents for pharmaceutical equipment.
• Travel to client sites for design, validation, and project support.
• Assist in developing and executing QMS procedures and regulatory reports.
• Perform investigations, troubleshoot validation issues, and prepare validation reports.

What You’ll Bring

• Strong communication skills and ability to interact with all management levels.
• At least 3 years of validation experience in automation, packaging, utilities, or facilities.
• Experience in pharmaceutical or biotech environments is preferred.
• Technical writing skills and proficiency with MS Office, Project, and AutoCAD.
• B.S. in Bioengineering, Biomedical, Chemical Engineering, or related field.

Additional Information

We foster an environment of respect, integrity, and professional growth. We encourage candidates from diverse backgrounds to apply and offer accommodations during the interview process.

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