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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Seattle, WA
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Portland, OR
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added just now
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Los Angeles, CA
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added just now
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
San Diego, CA
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added just now
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Atlanta, GA
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Raleigh, NC
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Indianapolis, IN
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Memphis, TN
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Salt Lake City, UT
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
San Jose, CA
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Minneapolis, MN
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Irvine, CA
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Boston, MA
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 1 min ago
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R&D Engineer II / Senior R&D Engineer - Medical Devices
GPAC
Charlotte, NC
- $80,000 to $130,000 USD / year
An established medical device manufacturer in Mecklenburg County, NC is hiring an R&D Engineer II / Senior R&D Engineer to design and develop Class II and Class III medical devices across…
Added 3 mins ago
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Lead Principal Platform Software Engineer
Oracle
Nashville, TN
- $113,600 to $306,400 USD / year
We are seeking a Lead Principal Software Engineer to set long-term technical direction for the Robotics Automation Platform. You will lead architecture and technical delivery across…
Added 3 mins ago
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Manager, Application Software Engineering
Oracle
Austin, TX
- $114,600 to $234,600 USD / year
· Establish practices that maintain code quality, security, and engineer accountability.
Added 38 mins ago
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Vice President, Data Systems
The Los Angeles Lakers, Inc
El Segundo, CA
- $275,000 to $300,000 USD / year
Engineering Excellence and Operations: Set and enforce software and data engineering best practices: version control, code review, CI/CD, infrastructure-as-code, automated testing,…
Added 53 mins ago
Quality Engineer / Principal Quality Engineer 2/3
Northrop Grumman
Elkridge, MD
May participate in the areas of design, incoming material inspection, production control, product evaluation and reliability, inventory control and/or research and development as they apply…
Added 53 mins ago
Sentinel - Principal / Sr Principal Systems Engineer - 19242*
Northrop Grumman
Roy, UT · Roy
Northrop Grumman Defense Systems is seeking a Principal Systems Engineer/Sr. Principal Systems Engineer. This opening is in Roy, UT and will support the Sentinel Program. Northrop Grumman…
Added 53 mins ago
Sentinel - Staff Systems Engineer - Lab Test Capability Lead
Northrop Grumman
Roy, UT · Roy
Northrop Grumman Defense Systems is seeking a Staff Systems Engineer - Lab Test Capability Lead to join the Sentinel Systems Engineering team located in Roy, UT. Northrop Grumman supports…
Added 53 mins ago
Spirit Defense - Associate Manufacturing Engineer
Spirit AeroSystems
Wichita, KS
Using the established manufacturing process flow, defines sequences of events, develops text and graphics work instructions, manufacturing datasets, tooling requirements, and manufacturing…
Added 54 mins ago
Engineer / Principal Engineer Manufacturing
Northrop Grumman
Baltimore, MD
Northrop Grumman Mission Systems is seeking a Manufacturing Engineer / Principal Process Engineer for the Advanced Interconnects and Multilayer Solutions (AIMS) manufacturing cell.
Added 54 mins ago
Manufacturing Process Engineer / Principal Manufacturing Process Engineer
Northrop Grumman
Baltimore, MD
Northrop Grumman Mission Systems is seeking a Manufacturing Process Engineer / Principal Manufacturing Process Engineer for the Advanced Interconnects and Multilayer Solutions (AIMS)…
Added 1 hour ago
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Quality Engineer - Manufacturing Job
GPAC
San Antonio, TX
- $70,000 to $110,000 USD / year
We are seeking a highly motivated Quality Engineer to lead and manage advance quality control activities for new product launches. As a Quality Engineer, you will be responsible for…
Added 1 hour ago
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Quality Engineer - Manufacturing Job
GPAC
Seguin, TX
- $70,000 to $110,000 USD / year
We are seeking a highly motivated Quality Engineer to lead and manage advance quality control activities for new product launches. As a Quality Engineer, you will be responsible for…

GlaxoSmithKline LLC

Associate Automation Engineer - 2nd Shift

King of Prussia, PA, United States

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Job details

Posting language: English
Posted: Oct 20, 2026

Original job description

We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021. We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. As a Associate Automation Engineer 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. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following 1. 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. 2. Troubleshoot and diagnose problems with process controls and manufacturing execution systems; generate recommendations and then develop/execute solutions to correct and resolve. 3. Drive continuous improvement and support capital projects. 4. Adhere to, develop, and continuously improve the operation and maintenance procedures for process controls and manufacturing execution systems. 5. 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. 6. Work in a way that models respect for safety and EHS, quality compliance, data integrity, and engineering standards. 7. Generate and maintain automation design specification and functional specification documents and ensure documents maintain good GxP documentation. 8. Communicate with different operational groups to understand the process and business operations and communicate technical issues and opportunities back to the automation team. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: 1. Bachelors degree 2. 1+ years working in a Good Manufacturing Practices (GMP) environment Preferred Qualifications: If you have the following characteristics, it would be a plus: 1. BS/BA in Engineering, Life Sciences, Biology, Electrical, Chemical, Process or Software Engineering 2. A demonstrated capability to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines is required 3. Ability to communicate problems and escalations to peers within the Automation team as well as other stakeholders 4. Shows the aptitude for prioritization and multi tasking to ensure the team is meeting the needs of stakeholders 5. Good interpersonal skills and the ability to work and succeed in a team environment 6. Highly motivated and elf-driven with a desire to continuously improve own skill set. Able to function productively with minimal supervision 7. Prior education or experience in the design, programming, and troubleshooting of Emerson Syncade, DeltaV or similar MES/DCS systems. 8. Experience working in or understanding of a GMP environment. 9. Knowledge in current standards of control system platforms and computer system validation. Skills Asset Life Cycle Management, Data Integrity, Digital Fluency, GxP Regulations, Lean Management, Manufacturing Technologies, Pharmaceutical Manufacturing, Problem Solving, Risk Awareness, Standards Compliance Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed witho

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