DeltaV Automation Engineer – Biotech Manufacturing

BioSpace

Holly Springs (NC)

On-site

USD 110,000 - 160,000

Full time

21 hours ago
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Job summary

Amgen is seeking a Senior Manufacturing Systems Engineer DeltaV to lead automation projects in the Facilities & Engineering group. You will drive process control solutions, design and qualify equipment, and support 24/7 manufacturing operations for robust drug substance production.

Ideally you bring strong DeltaV expertise, capital project experience, and leadership/mentoring skills to guide a team in a fast-paced biopharmaceutical environment while ensuring compliance with 21 CFR Part 11 and

Qualifications

  • High School Diploma / GED with 10 years engineering experience.
  • Associates Degree with 8 years engineering experience.
  • Bachelor's Degree with 4 years engineering experience.
  • Master's Degree with 2 years engineering experience.
  • Doctorate Degree.

Responsibilities

  • Lead technical projects and drive automation engineering improvements across upstream, downstream, and solution prep.
  • Partner with capital project team to design, build, commission, and qualify new equipment and systems for drug substance production.
  • Develop domain expertise to support operations at start-up and scale.
  • Mentor and develop site automation staff to accelerate capabilities.

Skills

Automation engineering
Leadership
Technical writing
Communication
Mentoring

Education

Bachelor's Degree in Engineering
Associates Degree
Master's Degree in Engineering
Doctorate Degree
High School Diploma / GED

Tools

Emerson DeltaV
OPC
Foundation Fieldbus
Profibus

Job description

Amgen is seeking a Senior Manufacturing Systems Engineer DeltaV to lead automation projects in the Facilities & Engineering group. You will drive process control solutions, design and qualify equipment, and support 24/7 manufacturing operations for robust drug substance production.

Ideally you bring strong DeltaV expertise, capital project experience, and leadership/mentoring skills to guide a team in a fast-paced biopharmaceutical environment while ensuring compliance with 21 CFR Part 11 and

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