On-Site Quality Auditor – Contract, CAPA & Compliance

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

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.