Quick Overview
Seniority
Mid Senior
Work mode
On Site
Location
Raleigh, NC, United States
Posted
5 days ago
FDA Regulations
Job Description
Title: DeltaV Automation Engineer (Biotech/Pharmaceutical)
Location - Raleigh - Durham NC
Various years of experience:
3 - 7 years /7 - 14 years/14+ years
Candidates need to be local or willing to relocate to the areas of operation where we have open opportunities for immediate hire in the Raleigh - Durham NC area:
Mandatory Skills:
3+ years of work experience with Emerson DeltaV
3+ years of work experience with DeltaV
Responsibilities
- Design, configuration, integration and implementation of process control solutions for the Life Sciences industry.
- Design, program, implement, test and document Emerson Delta V DCSs.
- Develop User Requirement Specifications.
- Develop Software and Hardware Design Specifications.
- Develop control system validation/testing protocols.
- Develop electrical panel schematics.
- Develop scope of supply documents.
- Manage automation projects as assigned.
- Monitor progress of projects.
- Install, test, and start-up control systems on-site.
- Work with plant engineers and operators to implement control strategies.
- Train operators and engineers on control systems.
Qualifications
- Requires a bachelor s or master s degree in mechanical engineering, Chemical Engineering, or related discipline degree is required.
- Minimum of five (5) years experience in the biotech/pharma industry.
- Strong knowledge of the S88 Batch structure is required.
- Strong knowledge on review and understanding of P&IDs drawings.
- Strong knowledge of automation narratives and architecture of DeltaV experience is a must.
- Experience in commissioning and startup of control systems is required.
- Experience with PLC, HMI, and SCADA systems is a plus.
- Experience with control system networking technologies and PC networking technologies is a plus.
- SCADA Platforms: Rockwell, Siemens, Wonderware, GE knowledge is a plus.
- Specific knowledge of cGMPs and batch process control in the life science industry.
- Knowledge of regulatory compliance inclusive of cGMP, 21 CFR Part 11 requirements, FDA regulations
Regards
Rajesh
Arrowminds Inc
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