Microbiology QC Technician - GMP Lab (First Shift)

Novo Nordisk A/S; West Lebanon (NH); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Annual bonus

Paid time off

401K match

Parental leave

Product access

Job summary

Novo Nordisk's West Lebanon site in New Hampshire seeks a Quality Control Technician for a Sun-Thu schedule. You will assist the Microbiology QC lab with day-to-day testing, workspace preparation, sampling, and equipment cleaning in a GMP/GLP setting.

The role emphasizes meticulous documentation, strict SOP adherence, and contributing to investigations. Prior GMP or life-science experience is preferred but not required; onsite at the West Lebanon facility.

Qualifications

• High School Diploma required.
• Associates Degree in a scientific field preferred.
• Three years of relevant work experience required with HS diploma.
• Associates Degree with zero years of relevant experience preferred.
• Pharmaceutical, Biotechnology or other regulated industry experience is preferred.
• Good organizational, time management and documentation skills.

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 investigations and problem solving.
• Documents and archives work in accordance with Good Documentation Practice.

Skills

Attention to detail

Documentation

Time management

Basic computer skills

Education

High School Diploma

Associates Degree (preferred)

Job description

Novo Nordisk's West Lebanon site in New Hampshire seeks a Quality Control Technician for a Sun-Thu schedule. You will assist the Microbiology QC lab with day-to-day testing, workspace preparation, sampling, and equipment cleaning in a GMP/GLP setting.

The role emphasizes meticulous documentation, strict SOP adherence, and contributing to investigations. Prior GMP or life-science experience is preferred but not required; onsite at the West Lebanon facility.