DeltaV Automation Systems Engineer - Singapore - Rovisys Asia Company Pte. Ltd.

    Rovisys Asia Company Pte. Ltd.
    Rovisys Asia Company Pte. Ltd. Singapore

    1 month ago

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    Full time $60,000 - $100,000 per year Engineering / Architecture
    Description

    We are looking to hire Senior DeltaV System Programmer to join our team working at our client site, a pharmaceutical MNC. The selected candidate will be required to design and implement control systems strategies utilizing the DeltaV DCS platform the Life Sciences Manufacturing industries.

    Responsibilities:

    • Work in team environment with engineers and designers from RoviSys, partners and clients to provide state of the art Control Systems to improve efficiency, product quality, and profitability of process manufacturing.
    • Work with automation team to design and implement distributed control system (DCS) in line with S88 standards for the plant.
    • Participate in system architecture, Design Specification, Control Strategies, and library development.
    • Testing and on-site commissioning and qualification of control systems
    • Develop Life Cycle documents, Electrical panels, Control Architecture and wiring drawings per GMP standards.
    • Supporting manufacturing operations for day-to-day support for Automation systems.
    • Develop engineering standards to improve efficiency and accuracy of project execution.

    Requirements:

    • Bachelor's in engineering or related fields.
    • 3+ years of experience in a similar role, ideally in the Pharmaceutical industry, with projects or operations.
    • Hands-on experience with up-to-date Emerson DeltaV DCS platform.
    • Understanding of Batch S88 standards (CM, EM, Phases, Recipes, Units etc).
    • Understanding of automation hardware and networking technologies.
    • Motivated self-starter who is quick to adapt and work with minimal supervision.
    • Strong analytical and problem-solving abilities.
    • Good interpersonal and presentation skills for presentation to clients/management team where necessary.
    • Experience and/or interests in pharmaceutical & biologics GMP processes (e.g. computer systems validation).