Net2Source (N2S)
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This range is provided by Net2Source (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 Net2Source (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
#J-18808-Ljbffr
This range is provided by Net2Source (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 Net2Source (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
#J-18808-Ljbffr