Controls and Automation Engineering

Company: Disability Solutions
Location: Zebulon
Posted on: May 24, 2025

Job Description:

Site Name: USA - North Carolina - ZebulonPosted Date: May 21 2025Are you looking for an opportunity to analyze and develop solutions to engineering problems related to manufacturing equipment and systems to determine causes of component failures? If so, this is the role for you.As an Automation Engineer you will be responsible to execute the major elements of the site Automation Strategy and provide Lead Process Automation expertise (Pharmaceutical Fill/Finish/Packaging) to the Zebulon site within a multi-disciplinary and extended team of Automation, Instrumentation, IT, Control engineers, external contractors and consultants. To successfully deliver compliant (financial, regulatory (e.g. cGMPs), GAMP) instrumentation, automation, business and control systems for new and existing pharmaceutical facilities, Building Management Systems and Environmental Monitoring Systems at ZebulonThis role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Maintain a detailed and expert knowledge of current and future automation technologies and be the site expert in a minimum of 3 of the following disciplines: Field Instrumentation, PLC, SCADA, Historians, Manufacturing Execution Systems, Virtualization and Integration Technologies - middleware, OPC, XML.
• Responsible for the delivery of high value automation projects to meet business requirements in terms of functionality, cost, quality and time.
• Provide process automation expertise and lead safety assessments where appropriate. Ensure compliance with all roles related GSK policies, procedures and local codes.
• Interface and build robust partnerships with key site functions including Production, Technical, Planning, Engineering and Quality to ensure technology designs deliver agreed benefits. Participate on area extended management teams as necessary and actively manage automation group requests from the business for support or new projects.
• 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 (Standard work) to manage individual priorities and responsibilities.
• Deliver measurement and control of Quality Critical Attributes (QCA) and help develop the associated Process Critical Control Points (PCCP) through use of appropriate control systems to ensure predictable and stable process operations.
• Provide training and support for onsite Users / Engineers in Automation technologies and applications.
• Provide subject matter expertise to regulatory inspections and interact with auditors as necessary.Why you?Basic Qualifications:We are looking for professionals with these required skills to achieve our goals:
  • Bachelor's Degree in a Science or Engineering related discipline.
  • 5+ years detailed experience delivering Automation technology within the pharmaceutical industry.
  • Six Sigma and Lean Manufacturing experience; Black Belt or Green Belt desirablePreferred Qualifications:If you have the following characteristics, it would be a plus:
    • Master's Degree in a Science or Engineering related discipline.
    • Must include hands-on programming and trouble-shooting skills for Automation, Instrumentation and IT systems.
    • Ability to interface with operational and senior management within the organization.
    • Understanding of FDA PAT initiatives and the impact on the Pharma industry.
    • Technical expertise in several scientific and engineering 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) Programming, Historians (Aspentech) and SAP.
    • A sound understanding of Software testing (FAT / SAT) and commissioning procedures.
    • A sound scientific and engineering understanding of pharmaceutical secondary processing, preferably in a pilot or manufacturing environment.
    • Good knowledge of IT architecture management, data warehousing & implementation processes
    • 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.
    • Demonstrated project management skills.
    • Working knowledge and understanding of EHS Practices with respect to the installation of automated plant.
    • A good appreciation of FDA PAT initiatives and the impact on the Pharma industry.
    • SPC techniques and applied application to improve / measure product manufacturing and quality.
    • Proven track record in providing automation support and maintenance for instrumentation, automation and controls.
    • Excellent written and oral communication skillsAbout the Zebulon Site GSK's Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less 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 focused on Safety and Quality
      • Clean and GMP compliant work environment
      • Onsite cafeteria
      • Onsite gym
      • Temperature-controlled climate
      • Licensed, onsite Health & Wellness clinic #LI-GSK#Globalsupplychain#Featuredmanufacuringjobs 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 special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).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/ AgenciesGSK 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 without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.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/

Keywords: Disability Solutions, Greensboro , Controls and Automation Engineering, Engineering , Zebulon, North Carolina