Quality Control Technician (Tues-Sat)

BioSpace

West Lebanon, NH0–3 yrs57m agovia LinkedIn

About the Role

This position offers hands-on experience in a Microbiology QC lab, supporting day-to-day activities to ensure testing operations run smoothly. The role is based at the West Lebanon, NH bioproduction facility and operates on a Tuesday-Saturday schedule.

Key Responsibilities

  • Performs routine QC support activities (e.g., housekeeping, sanitizations, glassware cleaning, sample receipt)
  • Performs sampling with minimal support
  • Supports low complexity tasks (e.g., Spectroscopy, Bioburden Testing, Incoming Inspection of Consumables)
  • Performs routine equipment maintenance with support
  • Identifies deviations and may support systematic problem-solving and laboratory investigations
  • Documents and archives work in accordance with Good Documentation Practice
  • May support report writing activities
  • Performs all job duties and responsibilities in a compliant and ethical manner, adhering to all applicable healthcare laws, regulations, and industry codes.
  • Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions.
  • Other duties as assigned.

Requirements & Tech Stack

  • Experience in a GMP, Life Science, or laboratory environment is preferred but not required.
  • Familiarity with cGMPs, established manufacturing practices and procedures.
  • Compliance with quality regulations and guidelines.
  • Detail-oriented and comfortable following established SOPs.
  • Ability to diagnose/fix issues and contribute to investigations.
  • Maintain high standards of documentation and compliance.
  • Primarily supports Microbiology QC teams.
  • Onsite position.
  • First shift Tuesday-Saturday schedule.

Qualifications

Education and Certifications

  • High School Diploma required.
  • Associates Degree in a scientific field preferred.

Work Experience

  • High School Diploma with three (3) years of relevant work experience required.
  • Associates Degree with zero (0) years of relevant work experience preferred.
  • Pharmaceutical, Biotechnology, or other Regulated Industry Experience preferred.

Knowledge, Skills and Abilities

  • The ability to understand and execute established written instructions.
  • 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).
  • Knowledge of laboratory or manufacturing operations preferred.

Physical Requirements

  • 0-5% overnight travel required.
  • Ability to climb, balance, stoop, reach, stand, and walk.
  • Ability to push, lift, grasp, and feel.
  • Ability to speak, listen, and understand verbal and written communication.
  • Repetition involving 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 for close activities (reading, writing, analyzing) and determining accuracy and thoroughness of work.
  • Working environment includes noise, proximity to moving parts/equipment, use of ladders, exposure to chemicals, odors, fumes, and dust.

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