Job Description

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
• 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 QC operations in the microbiology area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. This position carries out routine QC testing and may support sampling, investigations, validations, projects and other related support activities for the manufacturing facility and process. This individual works with supervision on routine tasks and detailed instruction on new tasks. Previous experience in a GMP or GLP environment is a plus but not required. In addition to performing laboratory testing this role will be responsible for performing/writing laboratory investigations, deviations, and change requests within QC.

This role is first shift and works onsite Tuesday-Saturday. The level and job title of the hired candidate will be commensurate with experience.

Relationships

Reports to: Manufacturing Supervisor

Essential Functions

• Independently performs low complexity testing (e.g. Bioburden, Spectroscopy, Environmental Monitoring)
• Executes moderate complexity testing with minimal support (e.g. Microbial Identification, HPLC, SDS-PAGE)
• Performs high complexity testing with support (e.g. Bacterial Endotoxin, ELISA, UPLC)
• Completes routine equipment maintenance/calibration
• Supports equipment qualifications or method verification/validation activities
• Participates in deviations and laboratory investigations
• Update standard operating procedures with help
• Delivers training on low complexity tasks
• Performs troubleshooting with support
• Contributes to cLEAN activities (e.g. PDCA, SPS, VSM)
• Lead or support projects with limited scope
• Documents and archives work in accordance with Good Documentation Practice
• Identifies continuous improvement opportunities
• Present standard requests during audit/inspections
• 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

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.

Development Of People Not Applicable

Qualifications
Education and Certifications:

• Associate’s degree in a scientific discipline required
• Bachelor’s degree in scientific discipline preferred

Work Experience:

• Associate’s degree with three (3) years of relevant experience required
• Bachelor’s degree with one (1) year of relevant experience preferred
• Pharmaceutical, Biotechnology or other regulated industry experience preferred

Knowledge, Skills, and Abilities:

• Knowledge of laboratory practices required (such as aseptic technique, use of pipettes, pH etc.)
• The ability to understand and execute established written instructions is essential
• Good organization and documentation skills
• Strong Attention to detail
• Ability to prioritize tasks
• Ability to train others

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

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.