Position range in Grafton County $42k - $63k Per Year
Quality Control Analyst I - IV Micro
Novo Nordisk, Inc.
Occupation: Quality Control Analysts
Location: West Lebanon, NH - 03784
Positions available: 1
Job #: 329403
Source: Novo Nordisk, Inc.
Posted: 5/7/2025
Web Site: www.novonordisk-us.com
Job Type: Full Time (30 Hours or More)
Job Requirements and Properties
Job Requirements and Properties
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 Quality Control operations in the microbiology, analytical or inspection 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.
Relationships
Reports to: Supervisor of Quality Control
Number of subordinates with direct/indirect referral: n/a
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
Additional Information Help for Additional Information.
Additional Information
Help for Additional Information.
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 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
Quality Control Analyst I - IV Micro
Novo Nordisk, Inc.
Occupation: Quality Control Analysts
Location: West Lebanon, NH - 03784
Positions available: 1
Job #: 329403
Source: Novo Nordisk, Inc.
Posted: 5/7/2025
Web Site: www.novonordisk-us.com
Job Type: Full Time (30 Hours or More)
Job Requirements and Properties
Job Requirements and Properties
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 Quality Control operations in the microbiology, analytical or inspection 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.
Relationships
Reports to: Supervisor of Quality Control
Number of subordinates with direct/indirect referral: n/a
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
Additional Information Help for Additional Information.
Additional Information
Help for Additional Information.
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 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
Job ID: 476355317
Originally Posted on: 5/9/2025
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