Associate Process Professional

Associate Process Professional

Facility:
Manufacturing

Location:

Clayton, NC, US

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.

What we offer you:

• Leading pay and annual performance bonus for all positions
• All employees enjoy generous paid time off including 14 paid holidays
• Health Insurance, Dental Insurance, Vision Insurance – effective day one
• Guaranteed 8% 401K contribution plus individual company match option
• Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
• Free access to Novo Nordisk-marketed pharmaceutical products
• Tuition Assistance
• Life & Disability Insurance
• Employee 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.

Support people, equipment and processes for our operations areas to meet business and regulatory requirements. Relationships Reports to Manager. The role is responsible for collaborating with stakeholders related to assigned area.

• Work directly with production and QA to support deviation investigations, quick containments and root cause analysis
• Ensure compliance with standards
• Identify process needs and improvement opportunities for routine to minimally complex matters
• Perform process confirmations to ensure compliance and process improvements
• Responsible for reviewing BPRs as necessary
• Follow all safety & environmental requirements in the performance of duties
• Other duties, as assigned

Physical Requirements 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.)

Associate's degree in technology (engineering, technology or related field of study preferred) from an accredited university required May consider a High School Diploma or equivalent with a minimum of two (2) years of manufacturing experience required, preferably in a pharmaceutical manufacturing environment Minimum of one (1) year of manufacturing experience in a pharmaceutical manufacturing environment preferred Excellent written communication skills required GMP knowledge preferred System knowledge preferred Manufacturing experience preferred Pharmaceutical manufacturing experience a plus