Supervisor, Formulation / Filling - Weekend PM 3/4
Location: Bloomington
Posted on: June 23, 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 life-changing careers, and 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
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 In general, the position is responsible for increasing
the ratio of value to non-value activities and eliminating waste in
the overall production and supply chain from start to finish, for a
defined area or operations, while being held accountable for
processes, personnel, safety, compliance and meeting or exceeding
the client requirements within their operational area.
Relationships Reports to Manager, Form/Fill Essential Functions
Supervises the daily activities of business, technical support or
production team Typically manages 5-30 employees Sets priorities
for the team to ensure task completion; coordinates work activities
with other supervisors for up to 2 months in advance Decisions are
guided by policies, procedures and business plan; receives guidance
and oversight from manager Typically, does not perform the work
supervised Collaborates and communicates with support functions
Schedules employees and manages workload for operational area
Reviews and approves GMP documentation while ensuring safety and
GMP quality compliance Supports and leads continuous improvement
projects Hires, trains, motivates, leads, develops, and evaluates
staff. Takes corrective action as necessary on a timely basis and
in accordance with company policy. Ensures compliance with current
federal, state, and local regulations. Consults with Human
Resources Department as appropriate Informs personnel of
communications, decisions, policies, and all matters that affect
their performance, attitudes, and results 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. Development Of People Supervisory. Qualifications High
School Diploma/GED with a 2-4 year relevant experience required OR
Bachelor’s Degree with 1-2 years relevant experience required
Leadership experience preferred GMP experience preferred GMP
experience preferred Work Schedule: This is for a weekend PM shift
3/4. One weekend working Friday, Saturday, and Sunday - 3 days. The
following week working Thursday, Friday, Saturday, and Sunday - 4
days, rotating between these shifts over ubsequent weeks. Technical
Requirements Excellent written and verbal communication skills with
internal and external customers Ability to communicate complex
technical information to non-technical audiences Maintains data
integrity and ensure compliance with company SOP’s, specifications,
as well as cGMP, ICH, FDA, EMA regulations or guidelines Able to
lead difficult discussions with customers and subordinates and
drive the conversation to an acceptable resolution Able to combine
and interpret data from multiple disciplines and an understanding
of the full Biologics process with respect to specific area of
expertise Begin to provide reliable and defendable interpretations
of regulatory guidance for the customer Well organized with ability
to handle and direct multiple activities within the group
simultaneously Maintains staff by recruiting and hiring, employees,
developing personnel growth opportunities, supporting employee
motivation and providing strategic alignment with the Quality
Assurance Department and site initiatives Behavioral Requirements
Positions views and arguments appropriately to win support
Convinces others to take action Negotiates professionally in tough
situations Responds effectively to the reactions and positions of
others Understands internal and external stakeholder requirements,
expectations, and needs Balances the interests of multiple
stakeholders within team Acts fairly despite conflicting demands of
stakeholders (client programs and team) Leadership Requirements (if
applicable) Uses comprehensive knowledge of applicable principles,
concepts, and practices and/or techniques to lead projects within a
department, group, or team in a single function or focus Applies
technical and functional knowledge to design projects that
contribute to overall direction of department or discipline Manages
day-to-day activities with individual team Focuses on and regularly
communicates to team about priorities and sets aside identified
less critical tasks Makes implementation plans and assignments that
allocate resources appropriately to complete objective Looks for
obstacles and develops effective contingency plans with input for
department initiatives and team's projects Uses milestones to
diligently track and manage the progress of the team and own work
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: , Lawrence , Supervisor, Formulation / Filling - Weekend PM 3/4, Manufacturing , Bloomington, Indiana