Novo Nordisk Pharmaceutical Industries, Inc.

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Project Manager 2 - IT & Automation

at Novo Nordisk Pharmaceutical Industries, Inc.

Posted: 8/2/2019
Job Reference #: 77214
Keywords: computer, technical

Job Description

Requisition ID

Job Description
At Novo Nordisk, we want to make a difference. For more than 95 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. 
Help us bring quality to life. We are currently seeking top talent for our two pharmaceutical manufacturing facilities in Clayton, NC. 
Position Purpose:
Primary responsibility is to provide project management services for new IT & automation projects & processes.  Scope of projects includes computer systems, facility, utility, equipment & processes associated with the production of insulin products. 
Project management includes the following activities:
  • Refine business case with project owner/sponsor;
  • Establish & communicate quantifiable project benefits;
  • Refine & clarify project scope through  early project analysis with subject matter experts & owners to further substantiate project purpose
  • Provide clear goals so that the project secures effective use of time & resources & builds employee motivation;
  • Develop time/resource estimates to complete projects;
  • Develop bid packages, bid evaluation, & drive vendor selection.  Also work with procurement to create project specific contracts;
  • Responsible for financial project accountability through purchase order creation, management, invoicing, & cost forecasting
  • Monitor, & control project work with stringent follow-up on quality, schedule & budget so that the project delivers the desired end-product;
  • Manage, coordinate, & direct contract resources;  Coordinate & direct internal resources;
  • Ensure that the right amount of resources & competences is allocated to the project, negotiate project resources with Line of Business (LoB) management;
  • Report project performance to the relevant stakeholders;
  • Manage strategy development & implementation of change control, qualification, & validation for the project;
  • Archive all key project & test documentation in compliance with good documentation practices;
  • Ensure alignment with Global programs & other site projects to actively share best practice, knowledge, & visions.
  • Projects:
    • Leads project activities associated with large, medium sized projects.
    • Creates master plans for projects that outline all required activities associated with the projects.
    • Develop timelines & resource estimates to complete projects.  Requires no guidance & direction to complete these goals & needs no coaching or technical competencies for goal obtainment.  Serves as a source of expertise in the group for projects.
    • Completes projects within schedule & budgetary constraints with allotted resources.
    • Ensures systems & processes are validated in a compliant manner in accordance with FDA, EU & NN requirements.
    • Ensures commissioning activities during projects reduce changes to systems/processes after being placed under formal change control.
    • Leads cross functional teams to ensure all support systems (procedures, calibration, maintenance work orders, etc.) are in place for systems associated with projects.
  • Investigations:
    • Leads the closure of investigations per approved timeframes.  Requires no guidance & direction to complete these goals & needs no coaching on technical competencies for goal attainment.  Serves as a source of expertise in the group for investigations.
    • Leads cross functional teams to determine the root cause & corrective actions for problems associated with investigations.
  • Regulatory Audits: Project documentation is successfully reviewed during audits without compliance issues.
  • Change Control:
    • Completes accurate & timely assessments associated with change control activities.
    • Ensures change control activities for systems are completed in a manner in compliance with FDA, EU & NN regulations. 
    • Leads change control efforts for process improvements & identifies opportunities for improvements.
    • Leads cross functional teams during change control efforts & serves as a source of expertise.
  • Maintains Safe Work Environment.
Required Education:

BA/BS in Engineering, Computer Science, or applicable technical degree or directly related equivalent experience.
Desired Education:

MA/MS preferred
Required Experience:
Min. 5 years of project management experience from GxP Production (Pharmaceutical or Nuclear or Military), with emphasis on within IT &/or Manufacturing Automation. 
Technical/Process/Functional Knowledge: 
  • Excellent technical writing & oral communication skills.  
  • Excellent presentation & facilitation skills. 
  • Expert knowledge in being a project team leader with excellent negotiation & conflict resolutions skills.  Capable of establishing & communicating high standards & expectations for performance & holding team members accountable for results. 
  • Ability to interact with all levels of the organization. 
  • Able to operate with a high level of autonomy & authority. 
  • Strong analytical/reasoning, organizational & multi-tasking skills. 
  • High level understanding of infrastructure services & manufacturing automation systems.
  • Expert in cGMP documentation practice & understanding of change control processes. 
  • Expert understanding of validation/system development life cycle approach.
  • Basic computer skills including experience in the use of Microsoft word, power point, excel, etc.  
Demonstrated expertise in planning/organizing, managing execution, checking results, & revising the work plan for complex problems being resolved by cross functional teams.

Physical Requirements:
  • Occasionally moves equipment and\or supplies weighing up to 33 pounds within the facility using various body positions.
  • Constantly operates a computer and other office equipment using hands.
  • Able to travel internationally, up to 10% of the time.
  • Able to work in an open office environment with the possibility of frequent distraction.
  • Able to work the hours necessary to support a 24/7 continuous manufacturing operation.
  • Able to adjust schedule to work with colleagues in other international time zones.

At this time, Novo Nordisk is not currently hiring individuals for this position who now or in the future would require sponsorship for employment visa status.
Novo Nordisk is an Equal Opportunity Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity.

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.

Project Manager 2 - IT & Automation

Job Category
Information Technology