Senior Automation Engineer

Hamlyn Williams

North Carolina

On-site

USD 120,000 - 150,000

Full time

14 days+

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Benefits offered by this job

10% annual performance bonus
401(k) with employer match
4 weeks of paid vacation
12 weeks fully paid parental leave

Job summary

A leading recruitment agency is seeking a Senior Automation Engineer specializing in Emerson DeltaV systems for a pharmaceutical manufacturing role in North Carolina. This position involves leading initiatives impacting product delivery and compliance. Candidates should have minimum 5 years of relevant experience and strong knowledge of GMP practices. The role offers a competitive base salary of up to $150,000, a 10% performance bonus, and comprehensive benefits.

Qualifications

  • 5+ years experience with Emerson DeltaV systems.
  • Strong knowledge of GMP and validation/testing protocols.
  • Ability to independently work in regulated environments.

Responsibilities

  • Lead IoV testing and commissioning activities.
  • Diagnose, troubleshoot, and resolve complex issues.
  • Serve as a liaison between Automation, Engineering, QA, and Manufacturing.

Skills

Expertise in Emerson DeltaV systems
Hands-on experience in pharmaceutical manufacturing
Knowledge of GMP practices
Problem-solving skills
Collaboration skills

Education

Industry experience in automation

Tools

Emerson DeltaV DCS

Job description

1 day ago Be among the first 25 applicants

This range is provided by Hamlyn Williams. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$120,000.00/yr - $150,000.00/yr

Direct message the job poster from Hamlyn Williams

Process Controls & Automation Engineering (Contract) - USA

Position Title: SeniorAutomation Engineer – Pharmaceutical Manufacturing

Compensation: Up to $150,000 Base + 10% Annual Bonus (Based on Experience)

Position Summary:

We are seeking an accomplished Lead Automation Engineer with deep expertise in Emerson DeltaV systems and a proven track record of success in GMP-regulated pharmaceutical environments. This is a high-impact role embedded within a critical site in Sanford, NC, supporting new product introductions, leading IoV (Installation and Operational Verification) testing, and ensuring robust system performance across complex automation infrastructure.

As a senior member of the automation team, you will drive initiatives that directly impact product delivery, compliance, and operational efficiency. You will act as a technical authority on DeltaV, mentor junior engineers, and collaborate cross-functionally to deliver best-in-class automation support aligned with FDA and GMP standards.

Key Responsibilities:

  • Lead and execute IoV testing and commissioning activities for process automation systems in support of new product rollout and site expansion.
  • Provide expert-level support in diagnosing, troubleshooting, and resolving complex issues in Emerson DeltaV DCS across batch and continuous operations.
  • Serve as a key technical liaison between Automation, Engineering, QA, and Manufacturing teams to ensure seamless technology integration and adherence to GMP and site quality requirements.
  • Contribute to the development and enforcement of automation standards, procedures, and documentation in line with CFR Part 11 and other regulatory frameworks.
  • Participate in an on-call rotation (1 in 8), ensuring high availability and continuity of automation systems. (Phone carried during a 168-hour period.)
  • Support internal and external audits by maintaining system documentation and contributing subject matter expertise.
  • Provide mentorship and technical leadership to junior engineers and project team members.

Qualifications:

  • Minimum of 5 years of hands-on experience with Emerson DeltaV systems, preferably in a pharmaceutical or biotech manufacturing environment.
  • Strong knowledge of GMP practices, GAMP guidelines, and validation/testing protocols for automation systems.
  • Demonstrated ability to work independently in high-stakes, regulated environments with a proactive approach to system reliability and compliance.
  • Proven experience in cross-functional collaboration, process improvement, and automation lifecycle management.
  • Degree not required; equivalent industry experience and expertise are highly valued.
  • Base Salary: $120,000 – $150,000 (commensurate with experience)
  • Performance Bonus: 10% annually
  • Retirement: 401(k) with employer match
  • Time Off: 4 weeks of paid vacation
  • Parental Leave: 12 weeks fully paid (for both parents)

This is an excellent opportunity for a senior automation professional to lead critical initiatives, shape automation strategy, and play a pivotal role in a rapidly growing pharmaceutical operation.

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Engineering and Manufacturing
  • Industries
    Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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