Quality Control Process Technical Analyst
Company: Novo Nordisk
Location: Clayton
Posted on: July 10, 2025
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Job Description:
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. 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. The Position Provides support to Quality
Control (QC) by driving continuous improvement, optimization, and
innovation as well as leading systematic problem solving and change
requests. Works with members of the departmental leadership team to
share best practices with NN departments/sites & external vendors.
Based on assigned area of responsibility, may work with LIMS and/or
QC initiatives. Relationships Reports to Manager, QC Support.
Essential Functions Serve as QC Global LIMS Site SuperUser and QC
Static Builder responsible for training and building of QC methods
Responsible for driving continuous improvement, innovation, and
optimization projects Responsible for driving change requests and
assisting with large scale investigations (QMT) Lead & coach peer
analysts and leaders in problem solving for small-scale process &
quality issues Understand the processes of data evaluation and
trending, to include reporting findings to leadership Represent QC
on global level and interact/collaborate with other NN sites Follow
all safety & environmental requirements in the performance of
duties Other accountabilities, as assigned Physical Requirements
Moves equipment &/or supplies weighing up to 33 pounds within
the facility using various body positions. Ability to do close
precision work with their hands. Must be able to remain in a
stationary position (sitting and standing) 50% of the time. May
required corrected vision to 20/25 based on role. May require color
vision based on role. Occasionally ascends/descends a ladder. May
be required to work at elevated heights. Occasionally works around
odorous &/or hazardous materials. Qualifications Bachelor’s
degree in science or technical field from an accredited university
required or equivalent combination of education and experience
required May consider an associate degree in science or technical
field from an accredited university required with a minimum of
seven (7) years QC experience Minimum of five (5) years of QC
experience in a pharmaceutical or related (regulated) environment
required Leadership/Supervisory experience preferred Demonstrated
foundational understanding of processes, procedures & products
associated with assigned areas required Perform detailed analysis
of events & processes, develop appropriate responses to situational
needs, & convey information/results to various organizational
levels as appropriate required Demonstrated knowledge of adult
learning methodologies & can use multiple methods to train & coach
others within the department & organization preferred Knowledge &
understanding regarding departmental processes & their high-level
inter-relationships required (i.e. how they work together to
establish a system) Excellent verbal & written communication
skills, investigative writing skills, & computer skills (MS Word,
Outlook, Excel, PowerPoint, & LIMS) required Demonstrates ability
to manage multiple tasks/deadlines & prioritize properly based on
process needs & events required 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,
we’re 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 1-855-411-5290.
This contact is for accommodation requests only and cannot be used
to inquire about the status of applications.
Keywords: Novo Nordisk, Rocky Mount , Quality Control Process Technical Analyst, Science, Research & Development , Clayton, North Carolina