Job Information
Novo Nordisk Quality Control Coordinator in West Lebanon, New Hampshire
About the Department
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
12 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 is responsible for coordinating/supporting/assisting the Quality Control team including offsite and onsite calibrations, quality system interaction, management of sample collection and drop-off, communication of production schedule and ad-hoc testing requests, troubleshooting, performing a variety of highly diverse and complex administrative tasks and activities requiring sound planning, organization, judgement, adaptability, and accountability.
This position is located in West Lebanon, New Hampshire and will require onsite work and collaboration. It is a full time (40 hour per week) position and the standard schedule is Monday-Friday (8am-5-pm). We offer a competitive salary, commensurate with experience.
Relationships
Reports to: QC Supervisor
Essential Functions
Supplier calibration coordination responsibilities include both coordination of offsite calibrations and external suppliers performing on site calibrations
Requesting proposals/quotes from calibration/equipment suppliers
Create purchase order requisitions using internal electronic system including tracking / status of orders. Support team with tracking and forecasting the budget for calibrations
Scheduling/hosting/coordination with asset owners for site visits
Receipt, scanning, drop-off of QC Sample Receipt. Responsibilities include resolution of any sample submission errors
Sample management of RND and RND back-up samples
Planning of EM and Utility Samples
Reference Sample Management and RND sample management
Cross functional communication with various departments
Working in gLIMS
Data entry into Regulatory Asset Management System (RAM)
Work with supervisor on document-related projects. Implement process improvements within the team using cLEAN® concepts
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
Qualifications
Education and Certifications:
High School diploma or equivalent with a minimum of three (3) years relevant experience, or an Associate’s degree or equivalent with one (1) or more years of relevant experience
Work Experience:
Minimum of three (3) years related experience with high school diploma in Quality Control, Manufacturing, calibrations, or pharmaceutical industry preferred
1 year experience required with Associates degree or Bachelors’ degree
Knowledge, Skills, and Abilities:
The ability to understand and execute established written instructions is essential
Good organizational, time management and documentation skills
Attention to detail and ability to prioritize tasks
Basic computer skills (e.g. email, MS Word, database management)
Understanding standard operating procedures (SOPs)
Ability to manage multiple priorities
Ability to work independently
Strong organization skills
Physical Requirements
0-5% overnight travel required. The ability to climb, balance, stoop, reach, stand and walk. The ability to push, lift, grasp, and feel. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 10 pounds of force occasionally 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.
The working environment includes a variety of physical conditions including: noise, close proximity to moving parts and equipment, use of ladders, and exposure to chemicals; atmospheric conditions including: odors, fumes, and dust.
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.