DeltaV Automation Engineer (BiotechPharmaceutical)
Job Location:
Raleigh, WV - USA
Monthly Salary:
Not provided by the employer
Posted:
12 September 2026 (7 hours ago)
Application Deadline:
10 December 2026
Vacancies:
1 Vacancy
Job Summary
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 bachelors or masters 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