Operator II, Inspection (WPM - F, S, S)
Company: Novo Nordisk
Location: Bloomington
Posted on: July 12, 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. Our Bloomington, Indiana site
is a state-of-the-art facility where we have an integrated model
from process and formulation to clinical and commercial
biomanufacturing and drug product fill/finish and packaging. The
Bloomington campus is a recognized facility where talented teams
work with innovators to help develop, manufacture and supply
products to patients around the world. What we offer you: Leading
pay and annual performance bonus for all positionsAll employees
enjoy generous paid time off including 14 paid holidays Health
Insurance, Dental Insurance, Vision Insurance – effective day
oneGuaranteed 8% 401K contribution plus individual company match
optionFamily Focused Benefits including 14 weeks paid parental & 6
weeks paid family medical leaveFree access to Novo Nordisk-marketed
pharmaceutical productsTuition Assistance Life & Disability
InsuranceEmployee 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 Operate
and Maintain Manual, visual inpsection production process to
achieve production goals. Shift: WPM Fri -Sunday 6pm-7:30am This
will be the initial shift, but may change in the future due to
business needs, so candidates must be flexible for shift changes,
including working weekends. Relationships Reports to Manufacturing
Supervisor. Essential Functions Applies to Inspection and
PackagingHas developed skills through formal training or
considerable work experienceWorks within established procedures
with a moderate degree of supervisionEffectively trains other
employees on basic operations process flowDuties are clearly
defined, and methods and tasks are described in detail Safely
operates basic equipmentSupports cleaning and organizational
efforts, including maintaining visual factoryRequired to read,
understand, follow, and review GMP documentsParticipates in area
continuous improvement activitiesReports safety, quality concerns,
and recommends improvementsDemonstrates mathematical skills,
including the ability to perform addition, subtraction,
multiplication, division, and conversionsActively promotes and
demonstrates good communication and escalation InspectionPerform
inspection techniques for manual visual inspection product
familiesPerform inspection activities while sitting in a lighted
booth for a 12-hour shiftPerform inspection activities while
operating in a Semi-Automated Syringe Inspection system and a
Semi-Automated Vial Inspection SystemPerform inspection activities
within a fully automated inspection processAble to perform
on-the-job training within Semi-Automated and Automated activities
PackagingPerform basic packaging activities by constructing
secondary and tertiary containers for finished packaging
productsMust be able to stand for a 12-hour shiftMust be able to
perform manual packaging and labeling activities within complex
packaging operationsAble to perform on-the-job training for basic
packaging and labeling activities within complex packaging
operations Label ControlWorks autonomously OR with moderate
supervision within established proceduresRequired to read,
understand, follow, and review GMP documentsParticipates in review
panels to revise SOPs, WI’s, and other documentation in
EDMSDemonstrates mathematical skills, including the ability to
perform addition, subtraction, multiplication, division, and
conversionsCollaborates and communicates with support teamsUtilize
the assigned logbook to document workstation line clearancesEnsures
batch readiness by gathering materials and documents required for
such activitiesHigh attention to detail due to criticality of
labeling processVerification and inspection of printed labelsGather
and Issue pre-printed material componentEffectively trains other
personnelAbility to perform on-the-job training for fellow Label
Control Operators for non-PBA required tasks Qualifications High
School/GED requiredAssociate degree preferred1-2 years relevant
experience2 years GMP experience preferredTechnical
RequirementsProficient with Microsoft Office programs, Email,
Teams, etc.Ability to learn and use quality, operations software
such as ComplianceWire®, JD Edwards®, etc.Ability to understand and
apply cGMPs to everyday workDemonstrates proficient understanding
of the work tasks assignedExecutes procedures with high
qualityProficient understanding of pharmaceutical production
operationsCapable of learning unfamiliar principles or techniques
with trainingRegularly applies theories and principles for one’s
technical discipline Behavioral RequirementsAbility to see/hear and
read/write clear EnglishLead by example according to the Company's
values and cultureAbility to communicate effectively and
follow/retain detailed written and verbal instruction in an
accurate, timely, safe, and professional manner with supervisor,
group members, and other departments as necessaryAbility to manage
time effectively to complete assignments in expected time frame and
independently seek out additional work when tasks are completed
ahead of timeAbility to cooperate with coworkers within an
organized team environment or work aloneDetail oriented and well
organized with ability to work effectively under high pressure with
multiple deadlinesAbility to put aside personal opinions and focus
on business needs, department needs or group needs Leadership
Requirements (if applicable)Leads by example according to the
Company's values and cultureBuilds on contacts and relationships
with peersTakes initiative for personal and professional
developmentTakes initiative when necessary to address changes in
scope and procedural errorsBuilds trust and respect for self and
departmentExpected to fulfill and maintain designated trainer
requirements as neededPromotes compliance by providing respectful &
constructive peer-to-peer feedback Physical Requirements Frequent
sitting, standing, walking, reading of written documents and use of
computer monitor screen, reaching with hands and arms, talking,
writing, listening. Occasional stooping, kneeling, crouching,
bending, carrying, grasping. Frequent lifting and/or moving up to
10 pounds and occasional lifting and/or moving up to 50 pounds.
Must comply with EHS responsibilities for the position. Working
conditions will be Heating Ventilation and Air Conditioned
controlled. Ability to operate within a clean room environment as
needed. Must meet vision requirements. 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, Kokomo , Operator II, Inspection (WPM - F, S, S), Manufacturing , Bloomington, Indiana