Equipment Engineer

GlaxoSmithKline; Zebulon (NC); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Onsite cafeteria

Onsite gym

Temperature-controlled environment

Health & Wellness clinic

Job summary

GlaxoSmithKline seeks an experienced site engineer at Zebulon, NC, to lead mechanical and automation initiatives on a multi-disciplinary team. You will support production, maintenance, quality, and EHS to deliver capital projects that align with the Zebulon True North strategy.

Responsibilities include troubleshooting production equipment, managing FAT/SAT and commissioning activities, and mentoring junior engineers in automation technologies. On-site role with emphasis on safety and quality.

Qualifications

• Bachelor's degree required in mechanical, electrical, automation, chemical engineering or related discipline; 5+ years' relevant experience or AAS/technical diploma with 10+ years' experience.
• 5+ years' experience delivering mechanical and/or automation projects, technologies and troubleshooting in the pharmaceutical industry.
• Experience troubleshooting production equipment, instrumentation and controls.
• Experience preparing and executing FAT, SAT, loop checks and software testing for qualification.

Responsibilities

• Maintain expert knowledge of current and future pharmaceutical platform technologies, focusing on automation, control systems and mechanical processes.
• Deliver continuous improvement projects for functionality, cost, quality and schedule adherence.
• Collaborate with maintenance and production for day-to-day troubleshooting of production issues.
• Provide process expertise and lead EHS assessments; ensure compliance with GSK policies and local codes.
• Interface with stakeholders to ensure projects deliver benefits.
• Participate in cross-functional teams and manage multiple projects concurrently.
• Coordinate with Shared Services and Centers of Excellence to maintain standards.
• Ensure performance management systems (GPS and Standard work) are used to manage priorities.

Skills

Mechanical expertise

Automation troubleshooting

Instrumentation & controls

FAT/SAT testing

Regulatory inspections

Project management

EHS knowledge

Cross-functional collaboration

Education

Bachelor's degree in mechanical, electrical, automation, chemical engineering or related discipline

AAS/technical diploma + 10+ years' relevant experience

Tools

ISA standards

P&ID nomenclature

Instrumentation wiring diagrams

PLC programming (Rockwell, Siemens)

SCADA (RSViewSE, iFix, Wonderware)

MES (Propack, Aspentech)

SAP

Job description

Business Introduction

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary

You will execute the major elements of the site strategy and provide mechanical and automation expertise to the Zebulon site within a multi-disciplinary and extended stakeholder team including Production, Technical, Engineering, Maintenance, Quality, Facilities, Automation, and EHS; as well as external contractors and consultants. To successfully deliver continuous capital projects which drive the Zebulon True North Strategy, to include measurable deliverables in the areas of Quality, Safety, Sustainability, and Security of Supply. Provide day-to-day production support at the shop floor level, with a strong emphasis in mechanical, automation, instrumentation and controls troubleshooting; both for new and existing pharmaceutical production equipment, as well as peripheral support systems as business drivers dictate.

Responsibilities

• Maintain a detailed and expert knowledge of current and future innovative and diverse pharmaceutical platform technologies, with a strong emphasis in high level automation and control systems as well as cutting edge mechanical processes and systems.
• Responsible for the delivery of continuous improvement projects to meet business requirements in terms of functionality, cost, quality and schedule adherence.
• Partner with maintenance and production stakeholders to assist in day-to-day troubleshooting of production related issues as required.
• Provide process expertise and lead EHS assessments where appropriate. Ensure compliance with all role-related GSK policies, procedures and local codes.
• Interface and build robust partnerships with key site stakeholders including Production, Maintenance, Technical, Planning, Facilities, EHS, Automation and Quality to ensure projects deliver agreed benefits.
• Actively participate in area extended management teams, EIT's, technical investigations and multidiscipline project teams as necessary; while actively managing multiple projects simultaneously.
• Interface and partner with the GSK community of Shared Services, Centers of Excellence and other sites to contribute, share, and leverage technology and maintain standards as appropriate.
• Ensure performance management systems are in-use (GPS and Standard work) to manage individual and team priorities and responsibilities.
• Mentor fellow engineering, maintenance and technical stakeholders in mechanical and automation technologies and applications.
• Provide subject matter expertise (SME) in regulatory inspections and interact with auditors as necessary.

Why You?

Work arrangement

This position is on-site in the United States. Hybrid or remote work is not available for this role.

Basic Qualification

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• Bachelor's degree in mechanical, electrical, automation, chemical engineering or related discipline and 5+ years' relevant experience; or AAS/technical diploma plus 10+ years' relevant experience.
• 5+ years detailed experience delivering mechanical and/or automation projects, technologies and troubleshooting within the Pharmaceutical industry
• Experience troubleshooting production equipment, instrumentation and controls.
• Experience preparing and executing FAT, SAT, loop checks, and software testing for qualification.

Preferred Qualification

If you have the following characteristics, it would be a plus:

• Technical expertise in several scientific, engineering and/or automation areas including ISA standards, P&ID nomenclature, instrumentation and electrical wiring diagrams, communication networks, control panels, HMI, MES (Propack, Aspentech), SCADA (RSViewSE, iFix, Wonderware) and PLC (Rockwell, Siemens, ELAU Pack Drive) Programming, Historians (Aspentech) and SAP.
• A sound understanding of project qualification execution, including software testing, loop checks, and various other FAT, SAT, commissioning and qualification procedures.
• A sound scientific and engineering understanding of pharmaceutical secondary processing, preferably in a manufacturing environment.
• Broad and in-depth knowledge and practical experience of computer and application validation (preferably using GAMP methodology), cGMPs, and 21 CFR Part 11 in an FDA regulated environment.
• Solid experience in capital project management, including equipment and system validation lifecycle development and execution, project budget management, resource planning and schedule management.
• Working knowledge and understanding of EHS Practices with respect to the installation of production equipment, facilities and control systems.
• Proven track record in providing technical support and maintenance for mechanical equipment, instrumentation, automation and controls.
• Excellent written and oral communication skills.
• Ability to collaborate with production, maintenance, quality and external contractors and work independently when needed.

What we value in you

We look for people who put safety and quality first. You will join a team that values clear communication, practical support and continuous learning. We welcome applicants from all backgrounds and encourage people who bring different perspectives to apply.

About the Zebulon Site

GSK's Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largestGSKPharmaceuticalsecondary manufacturing site in North America. The site islocatedless than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount,Wilson,and Wake Forest.

Key differentiators about GSK and Zebulon:

• Our commitment to inclusion is seen as a critical advantage of ours
• Our focus on cultivating a positive work environment that cares for our employees
• Demonstrated opportunities for continued career growth driven by individual ambition
• Leaders that care about their teams and growth of both individuals and the company
• A priority focus onSafety and Quality
• CleanandGMP compliant work environment
• Onsite cafeteria
• Onsite gym
• Temperature-controlledclimate
• Licensed,onsite Health & Wellness clinic

#LI-GSK

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 [e-mail]

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.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/