Automation Engineer DeltaV
Automation Engineer DeltaV
Posted on :
09-08-2023
Employer Active
The job posting is outdated and position may be filled
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
This Automation Engineer is a key member of a diverse team of professionals executing process control projects. Resource must have an excellent understanding of heavy industry process control to develop and execute the project control strategies.
Responsibilities:
Generate Functional Design Specifications for the PLC/DCS system.
Generate S88 based batch code.
Generate and execute test documentation & protocols as part of a cross discipline team.
Red-line design documentation (FDS) and drawings.
Trouble shoot PLC/DCS software problems.
Raise and process change requests for hardware/software changes.
Qualifications:
B.S. degree in Engineering (Mechanical, Electrical, Chemical) or Applied Physics & Instrumentation or similar
Good understanding of automation systems
Minimum of 3 years DeltaV DCS, Siemens S7, PCS7, Allen Bradley/Rockwell RS Logix, or FactoryTalk experience
Experience in the Pharmaceutical Industry is preferred but not essential
Knowledge of GMP, GAMP, safety and environmental regulatory requirements
Good understanding of the production & utility processes.
Providing independent quality review and approval of system lifecycle documentation, such as plans, requirements, risk assessments, protocols and reports for new and modified systems. Providing independent quality review and approval of system changes. Supporting and approving computerised systems investigations and test deviations. Ensuring consistent approach to qualification, change and deviation management across systems being implemented on the project. Providing timely and pro-active QA IT support and guidance to facilitate project timelines, including close collaboration with the technical and business units. Where required, engaging with QA IT teams from other sites and capital projects to standardise and align approach to computerised systems compliance. Experience: Min. 5 years of experience in QA IT/CSV, CSV and/or a similar role in the pharmaceutical industry. Working knowledge of relevant regulations and industry standards. Proven ability to meet timelines, prioritise tasks and engage with stakeholders. Excellent communication skills. Project management experience will be an advantage. DeltaV
Employment Type
Full Time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
