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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 life-changing careers and 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 457000 square foot aseptic fill and finish site that is responsible for producing innovative injectable diabetes and obesity treatments. At PS AM youll join a global network of manufacturing professionals who are passionate about what they do.
What we offer you:
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.
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
Associates 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
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees the patients we serve and communities we operate in. Together were life changing.
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.
If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply please call us at 1-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.
Required Experience:
IC
Full Time