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Novo Nordisk Senior System Engineer - IT in West Lebanon, New Hampshire

About the Department

Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. It’s not your average production site – it’s a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. We’re looking for individuals who are self-starters with a strong work ethic to join our team. At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential?

The Position

This position is an expert for technical, quality, and project issues within the IT Solutions supporting product manufacturing and release. This person is expected to be knowledgeable of all aspects of Control Systems, and to work closely with management to provide the short- and long-term vision for IT Solutions at API M2-US.

Relationships

Reports to: According to the organizational chart

Number of subordinates with direct/indirect referral: n/a

Essential Functions

  • Responsible for the design and/or selection of instrumentation, control devices, control panels, and control/electrical power systems throughout the facility in collaboration with Site SMEs and key stakeholders

  • Improvement of IT Solutions to increase efficiency and compliance

  • Establish and maintain site design standards for all IT platforms, including hardware, software and instrumentation standards

  • Operational vendor management and contract negotiations with focus on Systems Integrators and OEM suppliers

  • Act as client interface, point of escalation and resolve client concerns, developing and reporting project results, technical guidance of a project from concept to delivery, detailed project planning, management of suppliers/contractors/Systems

  • Takes the lead with the troubleshooting, testing, validation, deployment and on-going maintenance of Systems

  • Normally receives minimal instructions on routine work and general instructions on new assignments

  • Support for resolution of deviations, investigations, and other quality issues

  • Work closely with cross-functional teams, including manufacturing, facilities, process engineering, quality, MSAT (Manufacturing Science and Technology), to enhance operational efficiency and support continuous improvement initiatives

  • Point person for complex process improvement and start-up activities involving control systems

  • Initiates project(s), tracks spending / budgets, creates scope of work, develops risk assessments, justification, cost estimates, implements purchase requisitions, funding requests and manages contracts

  • Provides direction and coordination to less experienced engineers, which includes mentoring, training, project oversight, support and advice on all aspects of IT solutions

  • Provides support for troubleshooting for the more complicated issues found with site control systems

  • Other duties as assigned

  • Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes

  • Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others

    Physical Requirements

    0-10% overnight travel required. The ability to climb. stoop, kneel, crouch, crawl, reach, stand, and walk. The ability to push, pull, lift, finger, feel, and grasp. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 33lbs/15kg of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Visual acuity to perform close activities such as: reading, writing, and analyzing; and visual inspection. The working environment includes a variety of physical conditions including: noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including: odors, fumes, and dust.

    Qualifications

  • Education and Certifications:

  • Bachelor’s degree in engineering or related discipline required

  • Master’s degree in engineering or related discipline preferred

  • Certified Control System Technician or a Certified Automation Professional from the International Society for Automation (ISA) preferred

  • Work Experience:

  • Bachelor’s degree with a minimum of nine (9) years of direct engineering required

  • Master’s degree with seven (7) years of direct engineering preferred

  • Biotechnology or pharmaceutical experience required

  • Knowledge, Skills, and Abilities:

  • Instrumentation & Control Device operation and troubleshooting

  • Programmable Logic Controllers

  • Supervisory Control & Data Acquisition Systems (SCADA)

  • Variable Speed Drives

  • Electrical systems such as 120 VAC, 24 VDC, 480 VAC, GAMP guidelines

  • Part 11 and Annex 11 requirements

  • NFPA codes related to Automation & Electrical work

  • Ability to develop new systems and reverse engineer existing systems

  • Lead external contractors for project execution; Manage a project from inception to production and long-term support

  • Execute design reviews and risk analysis

  • Microsoft Office Suite (Word, Excel, Visio, Project, & PowerPoint)

  • Excellent oral and written communication skills

  • Strong knowledge of Microsoft Windows Operating Systems and Networking systems (Ethernet)

  • Demonstrated experience working in a team-oriented environment

  • Experience and skills to lead and manage multiple complex tasks or projects

  • Strong knowledge and experience implementing FDA and EMEA Regulatory automation requirements

  • Knowledge of AutoCAD (ability to view, make minor changes) desired

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

    At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

    Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

    If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

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