At Impel Talent, we are proud to be supporting a global pharmaceutical manufacturer known for its innovation, technical excellence, and commitment to delivering life-changing therapies to patients worldwide.

With cutting-edge production facilities and a truly international team, this business has built  strong reputation for combining scientific rigor with scalable, high-quality manufacturing. As they continue to expand their U.S. operations, they are now seeking a Senior Automation Engineer to join their New Jersey site.

This role is critical in delivering best-in-class automation systems across manufacturing and utility environments, with a particular focus on Emerson DeltaV.

Key Responsibilities:

Design, implement, and support automation systems, with a strong focus on Emerson DeltaV DCS, across pharmaceutical manufacturing operations.

Oversee the commissioning, qualification, and validation of automation systems, ensuring alignment with GMP, FDA, and internal standards.

Translate process and operational requirements into scalable, compliant automation strategies in collaboration with engineering, production, and quality teams.

Develop and review URS, FDS, SDS, FAT, and SAT documentation to support lifecycle activities.

Troubleshoot and maintain automation systems to ensure optimal performance, data integrity, and minimal downtime.

Support system upgrades, migrations, and integration of new equipment and processes into existing control systems.

Contribute to design reviews and risk assessments to ensure compliance, functionality, and safety.

Act as a technical leader and subject matter expert in DeltaV, offering mentorship and guidance to junior engineers.

Ideal Profile:

Bachelor's degree in Automation, Electrical, Mechanical, or Chemical Engineering (or related field).

5+ years of hands-on experience in automation engineering within regulated pharmaceutical or biotech environments.

Proven expertise in Emerson DeltaV DCS design, configuration, and troubleshooting (required).

Strong knowledge of GMP, GAMP5, 21 CFR Part 11, and validation protocols.

Experience working in cross-functional project environments, including facility expansions and equipment integration.

Excellent communication, documentation, and stakeholder management skills.

Why Apply?

Join a globally respected pharmaceutical company expanding its U.S. manufacturing capabilities.

Lead critical automation initiatives in a high-growth, high-impact role.

Be part of a diverse and inclusive team committed to innovation and patient care.

Benefit from long-term career development in a supportive and forward-thinking culture.

Posted On: Wednesday, September 17, 2025