Operations Sampling Technician I

Novo Nordisk

Support daily cGMP warehouse operations in pharmaceutical manufacturing as part of Novo Nordisk's team. Engage in sampling, inspection, and compliance activities within a high-standard environment.

Posted 7/9/2026full-timeClayton • North Carolina • 🇺🇸 United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in cGMP warehouse operations, including inspection, sampling, and compliance with regulatory standards. Proficient in following Standard Operating Procedures and maintaining accurate documentation while supporting quality control and process improvement initiatives.

Highest-signal resume keywords

CGMP ComplianceBasic Laboratory TechniquesSampling Aseptic TechniquesProblem SolvingLIMS Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

InspectionSamplingSample ManagementShelf-Life Expiry InventoryStandard Operating ProceduresDocumentationRegulatory ComplianceProcess ImprovementBatch TurnoverLogbook Entries

Soft Skills

Attention to DetailCommunication Skills

Tools & Technologies

LIMS System

Certifications & Qualifications

High School DiplomaBioWorks Certification

Industry Keywords

GMP Regulated EnvironmentUS RegulationsEU RegulationsEnvironmental ComplianceSystematic Problem SolvingCLEAN Mindset

About the role

Key responsibilities & impact

Support all daily activities of a cGMP warehouse operation including inspection, sampling, sample management, shelf-life expiry inventory, Job Instructions (JI) & regulatory compliance.
Package samples for transport
Follow Standard Operating Procedures in performance of assigned duties
Support GMP Laboratory and Environmental Compliance through daily tasks and ensure compliance with training programs related to job functions
Partner with QC, QA, EM & support groups to ensure raw material release for production & resources to support schedules and enable the process to run optimally
Maintain CNC areas & performing routine cleanings and batch turnover
Complete all paperwork in a cGMP compliant manner
Participate in Systematic Problem Solving, cLEAN Mindset, and streamlining processes
Support validation & project activities as required
Sampling of Raw Materials from Bulk tankers, Pressurized Containers, IBC’s, drums & Palletized Material
Ensure all errors are addressed & corrected real time ensuring compliance with cGMPs
Record logbook entries & other associated forms/paperwork for the team
Follow all safety & environmental requirements in the performance of duties

Requirements

What you’ll need

High School Diploma or equivalent with a minimum of one (1) year of experience operating in a GMP regulated environment required
Associate’s degree in science or relevant field of study from an accredited university preferred
BioWorks Certification preferred
Basic laboratory, sampling aseptic & ID testing techniques required
Ability to read, write & understand product documentation & standard operating procedures with attention to detail & computer literacy required
Knowledge of US, EU regulations & guidelines in reference to classified areas, sampling plans & methods & application of GMP’s a plus
Ability to communicate technical information clearly in writing & presentations preferred
Demonstrated experience in practical problem solving & process improvements a plus
Experience in LIMS system a plus
Experience planning, organizing, executing, checking results & revising work plans a plus

Benefits

Comp & perks

Leading pay and annual performance bonus for all positions
All employees enjoy generous paid time off including 14 paid holidays
Health Insurance, Dental Insurance, Vision Insurance – effective day one
Guaranteed 8% 401K contribution plus individual company match option
Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
Free access to Novo Nordisk-marketed pharmaceutical products
Tuition Assistance
Life & Disability Insurance
Employee Referral Awards