Senior Application Engineer - PAS- X FP

Responsible for ensuring reliable & consistent operation of identified local manufacturing applications. Improve reliability of process control systems to meet current & projected customer, business & regulatory requirements through the following activities: People Focus, Equipment Focus, Standards “Gatekeeper”., Work primarily with production (shop floor) & corporate as a liaison ensuring application understanding & managing continuous improvement initiativesPresent initiatives & information accurately & explain industry jargon in a clear manner for customersSupport the identification of application requirements through relationship building & effective stakeholder managementGather information about stakeholders’ needs/process gaps & develop/implement action plans that support the production goalsProvide input to product feature enhancements & process improvementsProvide resolutions to system related issues & discrepanciesCoordinate & oversee software upgrades & releases to applicable systemsCoach & train colleagues & stakeholders in relevant areasSchedule & execute plans in coordination with manufacturing schedulesLead & manage large projects that involve specified application solutionsDevelop & maintain process application standards, specifications & maintenance plansOwn self development & initiative to understand the site process control systemsSupport audits & inspections as SME for specified process applicationsUtilize the appropriate cLEAN® tools within the main areas of Systematic Problem Solving, process improvement, & project managementOperate within compliance with a Quality Mindset that focuses on risk management & mitigationImplement effective Change ManagementSupport Corporate, local IT & local stakeholder initiatives & projectsFollow all safety & environmental requirements in the performance of dutiesOther accountabilities, as assigned

Ability to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time. (% can change on a case-by-case basis based on the role.), Bachelor’s Degree in IT/Engineering or related field of study from an accredited university required and a minimum of eight (8) years of IT or engineering experience in process-based manufacturing, utility &/or packaging systems requiredIn lieu of Bachelor’s Degree with a minimum of eight (8) years of IT or engineering experience in process-based manufacturing, utility &/or packaging systems, may consider an Associate’s Degree in IT/Engineering or related field of study from an accredited college or university required and a minimum of ten (10) years of IT or engineering experience in process-based manufacturing, utility &/or packaging systems requiredTechnical/Process/Functional Knowledge: Knowledgeable in the following applications or technologies: PAS-X, POInT, PLC, SCADA requiredOrganization/Planning: Organization/Planning: Proven expertise, (e.g., project management) in planning/organization & project execution, follow-up & completion requiredAbility to translate high level direction into actionable tasks that deliver results using cLean / Six Sigma methodologies a required

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

Leading pay and annual performance bonus for all positionsAll employees enjoy generous paid time off including 14 paid holidaysHealth Insurance, Dental Insurance, Vision Insurance - effective day oneGuaranteed 8% 401K contribution plus individual company match optionFamily Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leaveFree access to Novo Nordisk-marketed pharmaceutical productsTuition Assistance Life & Disability InsuranceEmployee Referral Awards

At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.

At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world., In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic “fill and finish” site that is responsible for producing innovative, injectable diabetes and obesity treatments. At PS AM, you’ll join a global network of manufacturing professionals who are passionate about what they do., At Novo Nordisk, we’re not chasing quick fixes - we’re creating lasting change for long-term health. For over 100 years, we’ve been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what’s possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we’re making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger - a legacy of impact that reaches far beyond today., Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 54,400 people in 80 countries and markets its products in around 170 countries. For more information visit novonordisk.com.

Our US Research & Development hub, located in the Greater Boston area, brings together the best talent to drive life science innovation. Located in Lexington, Watertown and Cambridge, our teams reflect the full scope of R&D, from early research through late-stage clinical development. We are building for the future by creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. By combining the speed and agility of biotech with the quality, resources, and stability of a large pharmaceutical company, our US R&D hub will benefit from the best of both worlds to develop new medicines that meet the needs of patients.