Pharmaceutical Process Specialist
1 week ago
We are seeking a Pharmaceutical Process Specialist to join our team at IPS. The successful candidate will have extensive experience in designing and implementing industrial control systems for pharmaceutical processes.
About the Team:
Our team at IPS is passionate about delivering world-class designs for our pharmaceutical clients. We are a caring and nimble team that takes pride in our work and strives to make a difference in the lives of people.
About the Role:
- Develop automation User Requirements Specifications (URS) based on customer needs.
- Actively collaborate with the process design and project teams to support the execution of successful project studies.
- Develop the design and specifications for DCS, PLC, and SCADA-based process control systems for IPS clients and projects.
- Collaborate with client counterparts to develop control systems concepts, architectures, and control platforms as applied to the client project.
- Identify, qualify, and collaborate with third-party system integrators as necessary to support project and company business objectives.
- Support business development for process automation design and implementation. Assist in proposals, estimates, presentations, and other sales and marketing documents.
- Assist process engineering development of P&IDs and process control requirements, as well as Functional Requirement Specifications (FRS).
- Work with end users and Original Equipment Manufacturers (OEMs) to coordinate the application of automation products.
- Support risk assessments, including SIL, LOPA, and HAZOP.
- Support IQ/OQ development and participate in systems analysis, validation, and verification.
Requirements:
- Bachelor's degree in engineering or equivalent degree from an accredited university.
- 10+ years of experience with industrial process control systems including DCS, PLC, and SCADA-based systems, of which ideally, 5 years of experience with pharmaceutical process instrumentation.
- Expertise in computer operation for engineering design programs and computer-aided drafting.
- Experience with the development of cGMP and GAMP automation lifecycle documents.
- Excellent interpersonal skills and presence to deal effectively with senior-level contacts.
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