Senior Automation Engineer – BAS & PLC (GMP)

amgen

Holly Springs (NC)

Hybrid

USD 115,000 - 156,000

Full time

14 days+
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Benefits offered by this job

Total Rewards Plan
Stock-based incentives
Flexible work arrangements
Retirement & savings plan

Job summary

Amgen is seeking a Senior Manufacturing Systems Engineer specializing in automation to lead BAS/PLC systems for a cutting-edge drug substance facility. You will drive engineering efforts across design, start-up, and operational readiness, aligning with GMP requirements and project timelines.

Join a team advancing biotechnology with a focus on safety, quality and reliability. The role offers hands-on engineering leadership, cross-functional collaboration, and opportunities to influence

Qualifications

  • Bachelor’s degree in Electrical Engineering or related field.
  • Master’s degree with 2 years of relevant experience is preferred.
  • GMP/biopharma automation knowledge and practice is required.
  • Familiarity with 21 CFR Part 11 and GMP documentation is essential.
  • Experience with building automation controls and PLC-based systems is expected.

Responsibilities

  • Provide automation technical leadership for BAS/PLC systems.
  • Collaborate with capital project teams on commissioning and qualification activities.
  • Develop and maintain engineering documentation for validated systems.
  • Support IV/ACO and QA validation in a GxP environment.
  • Own Change Controls, CAPAs, and deviations for assigned systems.
  • Lead FAT with vendors and ensure compliance with Amgen standards.

Skills

Automation leadership
PLC programming
BAS design
GxP knowledge
Data integrity

Education

Bachelor’s in Electrical Engineering
Master’s degree preferred

Tools

PLC systems
Field instrumentation

Job description

Amgen is seeking a Senior Manufacturing Systems Engineer specializing in automation to lead BAS/PLC systems for a cutting-edge drug substance facility. You will drive engineering efforts across design, start-up, and operational readiness, aligning with GMP requirements and project timelines.

Join a team advancing biotechnology with a focus on safety, quality and reliability. The role offers hands-on engineering leadership, cross-functional collaboration, and opportunities to influence

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