Quality Control Analyst

Astrix; New Hampshire; On-site; USD 38,572 - 39,950; Full time

Job summary

A leading staffing agency in New Hampshire seeks a Quality Control (QC) Analyst to support testing in a fast-paced pharmaceutical environment. You will perform critical quality checks and documentation to ensure compliance with GMP standards. Ideal candidates have a degree in a related field and 2-4 years of industry experience. This full-time position offers competitive pay based on skills and experience.

Qualifications

• Desired 2-4 years industry experience, ideally in a cGMP environment.
• Knowledge of in-process, lot release, and stability testing.
• Ability to uphold GMP standards and maintain quality records.

Responsibilities

• Perform in-process, lot release, and stability testing.
• Review assays and maintain accurate quality records.
• Identify deviations and ensure compliance with GMP.

Skills

Laboratory systems familiarity

GMP Quality Systems knowledge

Proficiency in Microsoft Office

Education

Bachelor’s or Associate Degree in Microbiology, Biochemistry, or related field

Tools

TrackWise

LIMS

Job description

This range is provided by Astrix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$28.00/hr - $29.00/hr

Quality Control (QC) Analyst - Release Testing/Environmental Monitoring

Overview

Be a key part of a team that ensures safe, effective pharmaceutical products reach the market. As a QC Analyst with one of our top clients, you’ll support testing of in-process and final drug lots, helping maintain quality and compliance in a fast-paced environment.

Type

Direct Hire

Rate

$28-$29/hr, dependent on experience level.

What You’ll Do

• Perform in-process, lot release, and stability testing
• Review assays and maintain accurate quality records (Deviations, CAPA, Change Control)
• Identify deviations and uphold GMP standards
• Collaborate with teams to meet production timelines and quality requirements

What We’re Looking For

• Bachelor’s or Associate Degree in Microbiology, Biochemistry, or related field
• 2-4 years industry experience, ideally in a cGMP environment
• Familiarity with laboratory systems and GMP Quality Systems (TrackWise, LIMS preferred)
• Proficiency in Microsoft Office

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Seniority level

Associate

Employment type

Full-time

Job function

Science

Industries

IT Services and IT Consulting