Pharma QA Associate: Impactful Compliance & Documentation

Pfizer; Andover (MA); On-site; USD 69,000 - 114,000; Full time

Benefits offered by this job

401(k) with company match

Paid vacation and leave

Health benefits

Job summary

Pfizer in Andover, MA is seeking a Quality Assurance professional to support GMP compliance and batch release documentation. You will review batch records, SOPs, investigations, and deviations, helping ensure products meet the highest quality standards and regulatory requirements.

The role requires a bachelor’s degree or equivalent, strong communication, teamwork, and problem-solving skills, plus experience with GMP/GxP.

Qualifications

• Bachelor's degree in a relevant field or equivalent experience.
• Experience in pharmaceutical manufacturing and GMP/GxP knowledge.
• Strong written and verbal communication skills.

Responsibilities

• Review and approve batch records and investigations.
• Review SOP revisions and validation documentation.
• Ensure documents for batch release are complete and accurate.

Skills

Quality assurance

GxP knowledge

cGMP

Communication skills

Problem solving

Teamwork

Documentation

Digital applications

Education

Bachelor's degree

Associate degree with 4 years

Tools

ERP systems

eBR

AI applications

Job description

Pfizer in Andover, MA is seeking a Quality Assurance professional to support GMP compliance and batch release documentation. You will review batch records, SOPs, investigations, and deviations, helping ensure products meet the highest quality standards and regulatory requirements.

The role requires a bachelor’s degree or equivalent, strong communication, teamwork, and problem-solving skills, plus experience with GMP/GxP.