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Quality Assurance Inspector

Job in Andover, Essex County, Massachusetts, 05544, USA
Listing for: Net2Source (N2S)
Seasonal/Temporary, Contract position
Listed on 2026-01-05
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector
Salary/Wage Range or Industry Benchmark: 22 - 25 USD Hourly USD 22.00 25.00 HOUR
Job Description & How to Apply Below

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This range is provided by Net2

Source (N2S). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$22.00/hr - $25.00/hr

Direct message the job poster from Net2

Source (N2S)

Job Title:
Quality Assurance Inspector/ QA Batch Record Reviewer

Location:
Andover, MA 01810

100% onsite

Duration: 12 months contract (potential to extend)

Type:
Entry-level QA position.

Location:
On the manufacturing floor (in suites).

Function:
Real-time batch record review and GMP walkthroughs.

Role Overview

The main function of a Quality Assurance Inspector is to ensure that products, materials, and processes meet established quality standards and regulatory requirements. A typical Quality Assurance Inspector performs batch record reviews and collaborates with production teams to maintain consistent product quality.

Job Responsibilities

Conduct batch record review, document review and perform QA on the floor responsibilities.

Collaborate with production and engineering teams to resolve quality issues.

Ensure compliance with internal procedures and external standards (e.g., ISO, FDA).

Participate in audits and support continuous improvement initiatives.

Perform real-time batch record review during manufacturing.

Conduct GMP compliance walkthroughs in production suites.

Collaborate with operators and multiple teams to ensure compliance.

Support QA activities on the floor, not just desk-based review.

Must-Haves

Education:

Bachelor’s degree in a science field (Biology or Chemistry preferred, but flexible).

Experience:

0–2 years acceptable (entry-level).

Prior experience with batch record review is a strong plus.

GMP experience is critical (must have).

Ability to work collaboratively with diverse teams and personalities.

Strong communication skills and adherence to company values.

Nice-to-Haves

Previous QA experience in a manufacturing environment.

Familiarity with pharmaceutical or biotech operations.

Skills

Strong attention to detail and analytical thinking.

Knowledge of quality assurance methodologies and regulatory standards.

Effective communication and documentation skills.

Ability to interpret technical drawings and specifications.

Familiarity with quality management systems and software.

Ability to gown in and out of manufacturing suites is required.

Soft Skills

Collaborative and adaptable.

Comfortable interacting face-to-face with operators.

Strong attention to detail and compliance mindset.

Seniority level
:
Associate

Employment type
:
Contract

Job function
:
Quality Assurance

Industries
:
Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research

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