Associate Process Professional

About The Department 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. 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. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today. 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. The Position 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. Essential Functions 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.) Qualifications Associate’s degree in technology (engineering, technology or related field of study preferred) from an accredited university requiredMay 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 We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. #J-18808-Ljbffr BioSpace