Process Engineer

4 weeks ago

Forest Park, Georgia, United States Novo Nordisk Full time
About the Department

At Novo Nordisk, we are committed to improving the quality of life for millions of people worldwide. Our company has a rich history of innovation and leadership in diabetes care, and we continue to push the boundaries of what is possible.

We operate three pharmaceutical manufacturing facilities in North Carolina, each playing a critical role in our supply chain. Our newest facility in Clayton, North Carolina, is a state-of-the-art API facility that produces ingredients for our innovative oral products.

As a member of our team, you will join a global network of manufacturing professionals who are passionate about their work. We offer a dynamic and supportive environment that fosters growth and development.

What We Offer
  • Leading pay and annual performance bonus for all positions
  • Generous paid time off, including 14 paid holidays
  • Health, dental, and vision insurance, effective day one
  • Guaranteed 8% 401(k) contribution, plus individual company match option
  • Family-focused benefits, including 12 weeks paid parental and 6 weeks paid family medical leave
  • Free access to Novo Nordisk-marketed pharmaceutical products
  • Tuition assistance
  • Life and disability insurance
  • Employee referral awards
The Position

We are seeking an Associate Process Engineer to join our team. In this role, you will be responsible for ensuring the successful ramp-up of process tracks and providing input on design and requirement documents.

You will work closely with our Department Manager/Senior Manager to develop and implement process improvements. Your expertise in planning and organization will be essential in executing maintenance activities and revising work plans for complex problems.

Essential Functions
  • Support the development of design and requirement specifications documents
  • Ensure the quality of equipment and processes
  • Support the creation of process tracks risk assessment documents, such as Requirement Risk Assessments (RRAs)
  • Participate in the creation of a project cGMP statement
  • Creation and participation in QRM risk assessments, such as Closed-Process, Cross-Contamination, Contamination, and Facility flows
  • Input and review of Process FMECA's for the Process tracks
  • Participation in design workshops with engineering suppliers
  • Input and review of Process Module Diagrams and Process Flow Diagrams
  • Input and review of Process Scheduling and Capacity Calculations
  • Support package in maintaining schedule adherence
  • Ensure coordination and collaboration between project and other site stakeholders
  • Gathering and ensuring knowledge transfer to project from DK sponsor site
Physical Requirements

This role requires the ability to move equipment and supplies weighing up to 33 pounds within the facility. You will also be required to operate and inspect manufacturing equipment using your hands and to work in a fast-paced environment.

You must be able to be on your feet for up to a 12-hour shift and may be required to work at elevated heights. You will also be required to wear latex gloves and to work in loud noise environments with hearing protection.

Qualifications

We are seeking a candidate with a Bachelor's degree in science or engineering, preferably in Mechanical, Electrical, Chemical, or Industrial engineering. You must have a minimum of one year of work-related engineering experience in manufacturing, design, maintenance, or process improvement.

You should be knowledgeable in Instrument and Electrical, Mechanical, Control/SCADA/PLCs, Process Improvement Methodologies, Root Cause Analysis (RCA), and Reliability Centered Maintenance (RCM). Proven expertise in planning and organization is also essential.

We are committed to creating an inclusive culture that celebrates the diversity of our employees, patients, and communities. We are an equal opportunity employer and welcome applications from qualified candidates.

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