Manufacturing Area Specialist I Position Available In Grafton, New Hampshire

Manufacturing Area Specialist I
Novo Nordisk, Inc.

Location:

West Lebanon, NH – 03784
Positions available: 1
Job #: 323085

Source:

Novo Nordisk, Inc. | NLX | BioSpace, Inc

Posted:

5/12/2025

Web Site:

www.novonordisk-us.com

Job Type:

Full Time (30 Hours or More) Job Requirements and Properties Job Requirements and Properties Work Onsite
Full Time Schedule
Full Time
Job Description Help for Job Description. Job Description Help for Job Description. Site New Hampshire, located in West Lebanon, is where Novo
Nordisk’s life-saving treatments are brought to life. Our
manufacturing facility produces a global supply of our
hemophilia and growth hormone product lines, as well as our next
generation of cutting-edge medications.

What we offer you:

• Leading pay and annual performance bonus for all positions
• 36 Paid days off including vacation, sick days &
  company holidays
• Health Insurance, Dental Insurance, Vision Insurance
• Guaranteed 8% 401K contribution plus individual company
  match option
• 14 weeks Paid Parental Leave
• Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and
  mentorship to grow and build your career.

Are you ready to
realize your potential? The Position This position has primary responsibility to support
manufacturing operations. Focus areas may include Training,
Documentation, Deviations, Change Control and Projects. Drives
the coordination and execution of process and equipment
improvement initiatives, reviews completed quality records,
generates quality deviation responses, drive investigations and
has ability to train technicians on processes and QMS systems.

Relationships Reports to:

According to the organizational chart Number of subordinates with direct/indirect referral: n/a Essential Functions

• Liaison between Production Support and Manufacturing for
  the coordination of process/equipment improvements and data trending/analysis
• Review/approval of completed process documentation
• Ability to train others on the manufacturing process and
  QMS systems
• Revise and create documentation (SOP, batch records, FT’s)
  associated with the manufacture of product, requiring minimal direction
• Ability to investigate and write up Deviation events
  utilizing Root Cause Analysis
• Incorporate pre-planned process improvements and cost
  reduction projects into manufacturing
• Ability to take on and manage multi-disciplined projects,
  with minimal supervision
• Understanding/application of quality systems
• Support of Health Authority inspections
• Possesses technical and systems knowledge and can research
  information outside of knowledge base
• May need to support hands-on manufacturing within the
  given area for production coverage
• Has ability to recognize problems and recommend solutions
  to problems based on technical understanding of the process
  and equipment
• Support activities in other departments as instructed by manager
• Performs all job duties and responsibilities in a
  compliant and ethical manner and in accordance with all
  applicable healthcare laws, regulations and industry codes
• Incorporates the Novo Nordisk Way and 10 Essentials in all
  activities and interactions with others
• Other duties as assigned Additional Information Help for Additional Information.

Additional Information Help for Additional Information. Physical Requirements 0-10% overnight travel required. The ability to finger, climb, and walk. The ability to speak, listen, and understand verbal and written communication. While performing this job employee work involves sitting most of the time with walking and standing required only occasionally. This position may lift up to 10 pounds frequently or constantly to lift, carry, push, pull or otherwise move objects. Visual acuity to perform close activities such as: reading, writing, and analyzing; and to determine the accuracy, neatness, and thoroughness of work assigned or to make general observations. Qualifications

Education and Certifications:

• High School diploma or equivalent with a minimum of six (6) years relevant manufacturing experience or a Bachelor’s degree or equivalent in a science or engineering discipline with three (3) or more years of experience

Work Experience:

• Six (6) years relevant manufacturing experience with High School Diploma or equivalent
• Bachelor’s degree or equivalent with three (3) years of experience
• Pharmaceutical or biotechnology strongly preferred

Knowledge, Skills, and Abilities:

• Requires functional understanding of cGMPs, established manufacturing practices and procedures, and compliance with Quality regulations and guidelines
• Ability to understand and execute established written instructions is essential
• Organizational skills and an ability to perform assignments with a high degree of attention to