Sr Project Manager - OFP (Bulk Processing) Job

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 new OFP tableting facility located in Durham, NC.
Position Purpose:
Responsible for the complete Project Management (personnel and processes) for Oral Finished Production (OFP) processes in the assigned area for a new facility/production line. Manages all aspects of the Project from conception through completion within scope, cost, quality & schedule requirements. Leads & manages the Project Management team so that stated project objectives & solution requirements are met in compliance with company procedures & standards.
Accountabilities:

• Responsible for defining overall scope, establishing detailed RFP for obtaining proposals from all required consultants (engineering, construction, cost estimations (IPC costs), equipment vendors, etc.).
• Ability to create detailed business case, & present, to Senior Management within NN & IPG for funding of project.
• Effectively organize & manage multi-disciplined project team to ensure successful completion of all project deliverables – including hiring, goal setting, performance management, employee development & engagement.
• Manage major milestones, schedules & monthly cost plans through the Clarity & PEM processes.
• Provide periodic project status to STC including risks/mitigations, financial updates, short/long term project outlook, etc.
• Responsible for managing project change control to ensure project remains within defined scope, budget & schedule.
• Extensive collaboration with other sites within NN and external stakeholders to gain best practices & equipment specifications that will transfer to Site Clayton.
• Responsible for adherence to mechanisms for monitoring project progress, intervention & problem solving with other line managers or personnel.
• Assist with any training required of personnel supporting the project.
• Ensure all facets of the project lifecycle align with expectations set forth by the STG &/or project owner, such as installation, troubleshooting, qualification & validation of equipment.
• Follow all safety & environmental requirements in the performance of duties.
• Manage, lead, & coach teams of Subject Matter Experts (SMEs) to ensure a high performing collaborative team environment. Provide continuous feedback, structure & accountability to improve team performance.

Required Qualifications:

• BA/BS in Engineering/Economics/Business Administration
• Minimum of five (5) years of experience in pharmaceutical or biotechnology environment.
• Minimum of nine (9) years proven leadership and project management in a manufacturing facility, including experience with:
  • Capital Investment Projects with major projects in excess of $20M
  • FP Product/Process Transfer Projects
  • Change Management Projects

Desired Qualifications:

• Advanced Project Management competencies obtained through relevant PM training or experience.
• Knowledgeable in core work processes & GMP concepts.
• Understanding of complicated product documentation & standard operating procedures with attention to high-level concepts.
• Demonstrates functional/business understanding as well as superior written & oral communication skills.
• Extensive knowledge of project management including the ability to create work plans & detailed project schedules.
• Proficient in problem solving, negotiation, conflict management & interpersonal skills.
• Ability to act as project lead & lead cross functional project teams in the development & implementation of projects.
• Ability to influence others on objectives & projects outcomes.
• Basic understanding of contractual documents.
• Ability to read/review design drawings (CAD) with a basic understanding of P&ID, HVAC & Electrical systems.
• Thorough understanding of technical documents such as URS, SAT, FAT & Validation Protocols.

Physical Requirements:

• Ability to work hours necessary to support project and/or production activities.
• Constantly operates a computer & other office equipment using hands.
• Up to 25% international travel could be required.
• Occasionally moves equipment and/or supplies weighing up to 33 pounds within the facility using various body positions.

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.
Requisition ID: 60488BR
State/Provinces: Durham
Job Category: manufacturing