About the Department
At Novo Nordisk, we are helping to improve the quality of
life for millions of people worldwide. 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 newer
Active Pharmaceutical Ingredients (API) facility in Clayton, NC
sits on 825,000 square-feet of state-of-the-art equipment, and
houses the Fermentation, Recovery and Purification in the
production of ingredients for Novo Nordisk’s innovative oral
products. At API, you’ll join a global network of manufacturing
professionals who are passionate about what they do.
What we offer you:
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Leading pay and annual performance bonus for all positions
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All employees enjoy generous paid time off including 14
paid holidays
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Health Insurance, Dental Insurance, Vision Insurance –
effective day one
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Guaranteed 8% 401K contribution plus individual company
match option
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Family Focused Benefits including 12 weeks paid parental
& 6 weeks paid family medical leave
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Free access to Novo Nordisk-marketed pharmaceutical products
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Tuition Assistance
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Life & Disability Insurance
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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
Lead a team of GMP Raw Material Specialists to establish a
comprehensive framework for release testing, ensuring procedures
are meticulously designed based on critical parameters, user
input, supply chain risk assessments, and authority
requirements. Focus on defining the control setup, including
storage, handling, and inspection levels, to meet company
release specifications and ensure top quality & compliance.
Relationships
Director.
Essential Functions
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Lead the team by coaching, mentoring, developing, and
overseeing daily activities, while establishing transparent
objectives and outcomes to guide task prioritization and
ensure deadlines are met with a strong focus on quality and safety
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Enhance the efficiency of the supply chain operations by
consistently adhering to established policies and procedures,
and by applying the principles of the PS production system in
line with the Novo Nordisk Way. This approach aims to remove
bottlenecks and maximize the use of resources and equipment
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Ensure the timely availability of raw materials & all
other critical components needed in the manufacturing
processes & support processes
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Maintain/develop Purchasing Specifications &
Procedures according to cGMP’s
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Ensure preparation of Control Strategies for materials
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Support and optimization to existing GMP materials
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Facilitate prompt and effective communication within the
team, across departments, and with stakeholders including ISM,
SoOp Warehouse, Man Dev departments, productions, Strategic
Sourcing, CMC, and QA as well as ensure the swift
implementation and coordination of new materials in SoOp
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Ensure effective project management by undertaking
strategic initiatives related to the introduction of new
materials, crafting comprehensive project plans, achieving
goals, milestones, and cost targets; pinpointing necessary
project resources; providing direction, and inspiring,
guiding, and coaching project team members
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Establish project plans for the introduction of new
materials or material changes based on customer demands &
production capacities, minimizing impact to production
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Establish and maintain working relationship with key
stakeholders by supporting development projects regarding new
GMP materials and supporting existing GMP materials
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Provide data to prepare line of business management &
Product Supply for challenges related material management
related issues. Responsible for giving input to & updating
assigned Balanced Scorecard Metrics & related departmental
KPIs within Supply Chain
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Drive ongoing enhancements in customer satisfaction by
actively seeking feedback and engaging in collaboration with
all stakeholders, both internal and external, while ensuring
that decisions are made with a commitment to the cLEAN principles
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Follow all safety & environmental requirements in
performance of duties
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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.)
Development of People
Supervisory
Ensure that reporting personnel have individual development
plans (IDP), with annual goals and measurements that are
consistent with the priorities of the business, and that interim
reviews are held so that their work is focused on those
priorities, and they understand their level of accountability
for results and the measurement process.
Ensure that the IDP forms include completed learning and
aspiration plans and are in place for all reporting personnel to
enable the achievement of goals and capability to assume
increased levels of responsibility.
Manage the application and communication of all Novo Nordisk
policies, procedures, and Novo Nordisk Way.
Qualifications
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Bachelor's Degree in Supply Chain Management, Science,
Math, Statistics or a relevant field of study from an
accredited university required
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Minimum of five (5) years of experience in Supply Chain
Management, Production Planning, Quality or manufacturing
required, preferably in the pharmaceutical or other regulated industry
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Minimum of three (3) years of direct leadership in a
manufacturing environment required, preferably in the
pharmaceutical or other regulated industry
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APICS Training & Certification, CSCP or CPIM a plus
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Experience leading/managing projects of various
sizes/complexity preferred
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Excellent verbal & written communication skills required
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Proven process improvement & problem-solving skills required
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Strong knowledge of LEAN concepts & Flow manufacturing
skills preferred
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Familiarity with SAP systems (BW, APO, ECC preferred) preferred
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In-depth understanding of Novo Nordisk production
processes as well as support processes such as maintenance,
calibration, validation, Quality Control & Quality
Assurance preferred
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Proven expertise in mentoring & staff development,
change management, planning & organizing, managing
execution & revising work plans for complex issues
addressed by cross functional teams 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.