USA - Quality Auditor - III - USD

Pfizer Inc; Andover (MA); On-site; USD 72,000 - 80,000; Full time

Benefits offered by this job

Comprehensive benefits package

Short-Term Disability (STD)

Long-Term Disability (LTD)

Life Insurance

Job summary

Pfizer Inc. in Andover, MA is seeking a Quality Auditor III for a 11-month contract to ensure products meet quality standards and regulatory requirements. This on-site role involves audits, documenting findings, and driving CAPAs.

You will review QC procedures, identify non-conformances, collaborate with cross-functional teams, and monitor corrective actions. Candidates should have 5–7 years in QA/auditing, strong communication, and familiarity with ISO 9001, GMP, and FDA regulations.

Qualifications

• Requires 5–7 years in quality assurance, auditing, or compliance roles.
• On-site role in Andover, MA.
• Experience with ISO 9001, GMP, and FDA regulations preferred.
• Proficiency in Microsoft Office and audit documentation tools.
• Contract role of approximately 11 months 28 days.

Responsibilities

• Review quality control procedures for adherence to standards.
• Identify non-conformances and recommend corrective actions (CAPAs).
• Collaborate with cross-functional teams to resolve quality issues.
• Monitor implementation and effectiveness of corrective actions.
• Assist in updating quality assurance policies and procedures.

Skills

Attention to detail

Analytical thinking

Verbal and written communication

Independent work

Quality management systems

MS Office and audit docs

Interpersonal skills

Education

HS diploma or GED

Associate or Bachelor's degree preferred

Job description

USA - Quality Auditor - III - USD (Contract)

Andover, MA, United States (On-site)

Contract (11 months 28 days)

Published 2 days ago

Analytical

Communication

compliance

CAPA

audit

Summary:

The main function of a Quality Auditor is to evaluate and ensure that products, services, and processes meet established quality standards and regulatory requirements. A typical Quality Auditor conducts audits, documents findings, and recommends corrective actions to improve compliance and performance. The Quality Auditor usually reports to a Quality Assurance Manager or Compliance Lead.

Job Responsibilities:

Review quality control procedures and ensure adherence to company and regulatory standards Identify non-conformances and recommend corrective and preventive actions (CAPAs).

Collaborate with cross-functional teams to resolve quality issues.

Monitor implementation of corrective actions and verify effectiveness.

Assist in developing and updating quality assurance policies and procedures.

Stay current with industry regulations, standards, and best practices.

Skills:

Strong attention to detail and analytical thinking.

Excellent verbal and written communication skills.

Ability to work independently and manage multiple audits.

Familiarity with quality management systems (e.g., ISO 9001, GMP, FDA regulations).

Proficiency in Microsoft Office and audit documentation tools.

Strong interpersonal and collaboration skills

Education/Experience:

High school diploma or GED typically required; associate or bachelor's degree preferred.

5-7 years of experience in quality assurance, auditing, or compliance roles

Pay Rate Range

Min Pay Rate $52

Max Pay Rate $58

Currency USD

Unit hourly

Additional Notes

Please note that contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.

This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.

Benefits Information

Comprehensive Benefits Package available based on eligibility

Short-Term Disability (STD)

Long-Term Disability (LTD)

Supplemental and Voluntary Life Insurance