Automation Engineer; onsite in MA
Listed on 2025-10-16
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Engineering
Systems Engineer, Electrical Engineering, Automation Engineering, Manufacturing Engineer
Join to apply for the Automation Engineer (onsite role in MA) role at Bio Space
Company Description
Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at Follow @abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok.
The Automation Engineer will be responsible for developing automation technologies and Manufacturing control systems to improve site productivity, quality and safety performance. In this dynamic role the Automation Engineer will ensure the success of Drug product manufacturing through an understanding and strong background in engineering, configuration, programming, installation, commissioning, maintenance and troubleshooting of process controls, automation, electrical devices and field instrumentation technologies.
Responsibilities- Support a Safe working environment by aligning with all pertinent environmental health, safety & maintenance program practices, rules, and regulations.
- Understanding of cGMP processing with change control, nonconformance, corrective & preventive actions, and Commissioning & Qualification activities.
- Experience with the following product platforms:
- Rockwell PLC Platform
- Emerson DeltaV
- Day-to-day Operational Support:
- 24 x 7 Onsite/On Call:
Rotational Support - Trouble shooting Support to Manufacturing
- Be a knowledgeable SME for Upstream and Downstream Unit operations by
- Trouble shooting activities in partnership with the Plant Engineering & Maintenance teams to enhance manufacturing uptime through the highest reliability of Automation systems.
- Being responsible for continuous improvement in partnership with Plant Engineering, Maintenance, Manufacturing, Process engineering and OPex to drive operational efficiencies.
- Responsible for collaborating within the Abb Vie network to learn, implement and share Continuous improvement opportunities within the Drug Product manufacturing Abb Vie Global network.
- This role involves the application of automation engineering principles in the design, specification, construction, startup, commissioning and qualification of process equipment and systems for capital projects of significant scope and complexity. Demonstrated understanding of project life cycles is preferred
- Candidate should be familiar with engineering processes from initial conceptualization through project turnover to operations. Responsible for developing & maintaining Engineering Specifications, documents, drawings, and Standard Operational Procedures (SOP) including Administrative SOPs and Job Aids.
- Provide Abb Vie User requirements to OEMs/System Integrators during the development of process control applications applying Programmable Logic Controllers (PLC), Human Machine Interfaces (HMI) and Supervisory Control and Data Acquisition systems (SCADA), and development of Batch Reports using MES platforms like POMS.
- Conversant with industry standards on quality and regulatory compliance requirements such as 21 CFR Part 11 (Data Integrity, User Security, System Disaster Recovery, Data Backup & Restore).
- Ability to communicate in the simplest business language at various partner forums in the workplace.
- Bachelors degree in Mechanical Engineering, Electrical Engineering, Computer Science, or related field is required.
- Minimum 2-4 years experience, developing and maintaining automation software and equipment and PLC systems in a manufacturing environment; AI and machine learning experience, including experience with new technology development for new product introductions.
- Direct experience with system development and validation, including development of system specifications (DS, FS, URS) and risk-based validation strategies, and validation protocol development and execution.
- Demonstrated knowledge of 21 CFR Part 11 requirements for automated systems in the pharmaceutical…
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