Associate Automation Engineer - 2nd Shift
GSK
Summary
Provide engineering and technical support for process controls and manufacturing execution systems in the Biopharmaceutical Operations facility for the specified shift support hours. Evaluate and develop technology, plan and implement modifications, troubleshoot and support process controls and manufacturing execution systems and assist in night shift troubleshooting activities during processing operations.
Job description
Responsibilities
- Provide technical support of site automation systems and network infrastructure during night shift support hours. Critical systems include DeltaV DCS and Syncade MES.
- As directed, support automation workstreams across the system development life cycle: gather system/end user requirements; complete design, implementation, and testing/validation of changes; maintain documentation; maintain and monitor various systems.
- Troubleshoot and diagnose problems with process controls and manufacturing execution systems; generate recommendations and then develop/execute solutions to correct and resolve.
- Drive continuous improvement and support capital projects.
- Adhere to, develop, and continuously improve the operation and maintenance procedures for process controls and manufacturing execution systems.
- Support the maintenance and upkeep of the operational technology environment through work order execution and administration of systems, networks, databases, and accounts. This includes servers, hosts, and analytical equipment.
- Work in a way that models respect for safety and EHS, quality compliance, data integrity, and engineering standards.
- Generate and maintain automation design specification and functional specification documents and ensure documents maintain good GxP documentation.
- Communicate with different operational groups to understand the process and business operations and communicate technical issues and opportunities back to the automation team.
Basic Qualifications
- Bachelors degree
- 1+ years working in a Good Manufacturing Practices (GMP) environment
Preferred Qualifications
- BS/BA in Engineering, Life Sciences, Biology, Electrical, Chemical, Process or Software Engineering
- A demonstrated capability to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines is required
- Ability to communicate problems and escalations to peers within the Automation team as well as other stakeholders
- Shows the aptitude for prioritization and multi tasking to ensure the team is meeting the needs of stakeholders
- Good interpersonal skills and the ability to work and succeed in a team environment
- Highly motivated and self-driven with a desire to continuously improve own skill set. Able to function productively with minimal supervision
- Prior education or experience in the design, programming, and troubleshooting of Emerson Syncade, DeltaV or similar MES/DCS systems.
- Experience working in or understanding of a GMP environment.
- Knowledge in current standards of control system platforms and computer system validation.
Requirements
- Bachelors degree
- 1+ years working in a Good Manufacturing Practices (GMP) environment
- BS/BA in Engineering, Life Sciences, Biology, Electrical, Chemical, Process or Software Engineering
- A demonstrated capability to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines is required
- Ability to communicate problems and escalations to peers within the Automation team as well as other stakeholders
- Shows the aptitude for prioritization and multi tasking to ensure the team is meeting the needs of stakeholders
- Good interpersonal skills and the ability to work and succeed in a team environment
- Highly motivated and self-driven with a desire to continuously improve own skill set. Able to function productively with minimal supervision
- Prior education or experience in the design, programming, and troubleshooting of Emerson Syncade, DeltaV or similar MES/DCS systems.
- Experience working in or understanding of a GMP environment.
- Knowledge in current standards of control system platforms and computer system validation.
Benefits
- Comprehensive benefits program
Company overview
GSK plc (formerly GlaxoSmithKline) is a British multinational pharmaceutical and biotechnology company headquartered in London, England. Founded in 2000 through the merger of Glaxo Wellcome and SmithKline Beecham, GSK has grown to become one of the world's leading healthcare companies with operations in over 150 countries. The company specializes in researching, developing, and manufacturing prescription medicines, vaccines, and consumer healthcare products. GSK's therapeutic areas include respiratory diseases, HIV/AIDS, oncology, immunology, and infectious diseases. The company is particularly renowned for its vaccine portfolio and has been at the forefront of developing treatments for major global health challenges. With approximately 70,000 employees worldwide, GSK maintains a strong commitment to scientific innovation and has a significant presence in key markets including the United States, Europe, and emerging economies. The company's mission is to unite science, technology, and talent to get ahead of disease together, aiming to positively impact the health of 2.5 billion people by the end of the decade.