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PerkinElmer logo
PerkinElmer

For 85 years, we have pushed the boundaries of science with a clear purpose – to help our customers achieve theirs.

Senior Automation Engineer

QA Automation EngineerQA Automation EngineerOtherRemoteSeniorTeam 5,001-10,000Since 1938H1B SponsorCompany SiteLinkedIn

Location

California + 12 moreAll locations: California | Colorado | District of Columbia | Florida | Illinois | New Jersey | North Carolina | Ohio | Massachusetts | Missouri | Pennsylvania | Texas | Virginia

Posted

100 days ago

Salary

$130K - $165K / year

Seniority

Senior

Bachelor Degree9 yrs expEnglish

Job Description

Senior Automation Engineer

PerkinElmer

• Provides subject matter expertise in the design, implementation, and lifecycle management of automation systems across biologics, pharmaceutical, and novel therapy manufacturing facilities. • Develop full automation system architectures for biologics, pharmaceutical, and advanced therapy manufacturing. • Create ISA‑88/ISA‑95‑aligned architecture diagrams, I/O strategies, network topologies, and interface specifications. • Lead the creation, review, and approval of User Requirements Specifications (URS), Functional Requirements Specifications (FRS), and Design Specifications. • Configure, program, and deploy DeltaV DCS. • Develop, modify, and test Rockwell PLCs. • Support integration of OEM skids and commissioning, validation & GMP compliance.

Job Requirements

  • Bachelor’s degree in Engineering (Automation, Electrical, Chemical, Mechanical, or related)
  • Minimum 9-12+ years in automation engineering within GMP life sciences
  • Expert-level experience with DeltaV DCS and/or Rockwell / Allen Bradley PLC/SCADA platforms
  • Proven ability to author, interpret, and own URS/FRS/DS documentation
  • Experience designing system architectures across DCS, PLCs, SCADA, MES, OSI-PI and/or other historians and data systems
  • Strong understanding of ISA‑88 batch control, ISA‑95 manufacturing hierarchy, and GAMP 5
  • Hands‑on experience supporting biologics and sterile/aseptic manufacturing environments
  • Understanding multisite standards for global manufacturers
  • Applicants must be authorized to work in the United States on a full-time basis

Benefits

  • Health insurance
  • Professional development opportunities
  • Flexible work arrangements

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