Controls Engineer (PHARMA)

Actalent
Durham, NC Full Time
POSTED ON 5/11/2023 CLOSED ON 5/31/2023

What are the responsibilities and job description for the Controls Engineer (PHARMA) position at Actalent?

Description:

The Automation resource requested will be based at the Durham, NC, USA site. The scope of work will include, but not be limited

to:

1. Develop PLC /SCADA based system for two (2) formulations systems based on the same design as existing applications already

running in production. The expectation is to re-use all the PLC/SCASDA software applications that have been developed for the

line in production on the new line.

2. Configure and deploy a Rockwell Automation FactoryTalk Historian Server.

3. Configure and deploy a Rockwell Automation FactoryTalk SCADA Server.

4. Support the integration of the formulation and filling equipment as well as other ancillary equipment.

5. Create and/or update Control Panel, Electrical and I/O drawings.

6. Reading and verifying facility and equipment drawing (e.g., P&IDs, PFDs, etc.).

7. Create and Revise Lifecycle document (i.e., Design Specifications Documents, Functional Specification Document, Software

Specifications Document, etc.)

8. Support generation and execution of Installation and Operational Qualification of new hardware, software, equipment, and

instruments.

9. Support other Automation related project work as time permits

Additional Skills & Qualifications:

1. Bachelor of Science in Engineering or equivalent preferred. Equivalent experience will be considered in Lieu of Bachelor of

Science degree.

2. Minimum of 7 years’ experience designing, building, programming, debugging, and deploying Rockwell Automation/Allen

Bradley based system.

3. Experience with Studio 5000 Design Software, FactoryTalk View Studio, and RSLogix 5000

4. Experience with Rockwell Automation PlanPax.

5. Some Experience with FactoryTalk Historian or OSI PI

6. Experience in a GMP Manufacturing environment

7. Experience with set up and programming and Kinetix Servos and PowerFlex drives.

8. Experience in supporting creation and execution of Commissioning, Qualification, and Validation protocols (CQV)

9. Experience with design of Control Panel, Electrical and I/O drawings

10. Experience with Aveva/Wonderware System Platform and Intouch is a plus

11. Proficient with Microsoft Office – Word (advanced knowledge preferred), Excel, PowerPoint, Project.

12. Familiarity with US FDA (21 CFR 210, 211, 810) and EU EMEA regulations

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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