PharmEng Technology

Automation Engineer (MES)

PharmEng Technology  •  Holly Springs, NC (Onsite)  •  8 days ago
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Job Description

Job Title: Automation Engineer (MES)

Location: Holly Springs, NC (Onsite 4 days/week, 1 day remote)

Type: Long-Term Contract

About the Role:
We are seeking an experienced Automation Engineer to support the implementation and integration of DeltaV MES for drug substance manufacturing. This position involves configuring systems for paperless manufacturing with ERP/MES/DCS integration, troubleshooting, and collaborating with cross-functional teams to ensure smooth project execution.

Key Responsibilities:

  • Support the design and implementation of an Emerson Syncade (DeltaV MES) Manufacturing Execution System.
  • Participate in project status meetings and provide input on system requirements and lifecycle documentation.
  • Configure MES functions, including:
    • Order Management
    • Material Management
    • Workflow Execution
    • Electronic Batch Record (EBR)
    • Quality Review Manager (QRM)
    • Weigh & Dispense
  • Coordinate with Automation, CSV, CQV, Utilities, Process Engineering, QA, and other project teams.
  • Perform simulation of DeltaV MES logic and resolve issues.
  • Assist with configuration migration between sites and internal systems.
  • Develop and maintain Configuration Management processes to ensure data integrity.
  • Complete safety and project-specific training as required.

Experience & Skills:

  • 5+ years of experience designing, configuring, and implementing Manufacturing Execution Systems.
  • 3+ years of experience with Emerson Syncade (DeltaV MES).
  • Proficiency in debugging MES configuration.
  • Familiarity with cGMP standards, FDA regulations, S88 batch models, ISA 95, GAMP5, and 21 CFR Part 11.
  • Knowledge of VB Script, XML/XPATH/XSLT, and SQL/TSQL is a plus.
  • Experience with Emerson DeltaV, OSIsoft PI, and InfoBatch is advantageous.
  • Strong written and verbal communication skills.

Additional Details:

  • Expected to work 40 hours per week.
  • Onsite requirement: 4 days per week; 1 day remote.
  • Initial project duration: 6 months with potential extensions for future projects.
PharmEng Technology

About PharmEng Technology

PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.

As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.

Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.

At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.

Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).

Industry
Chemicals & Materials
Company Size
201-500 employees
Headquarters
Toronto, CA
Year Founded
Unknown
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