Quality Instrument Systems Specialist

Pfizer; Andover (MA); On-site; USD 83,000 - 138,000; Full time

Benefits offered by this job

401(k) matching

Pfizer retirement contribution

Paid vacation and leave

Health benefits

Job summary

Pfizer seeks a System Specialist at the Andover site to support Quality Control and Manufacturing Instrumentation lifecycle activities, including qualification, maintenance, troubleshooting, and data integrity within GMP environments.

You will contribute to validation/upgrade projects and generate documentation while collaborating with QC and GMP teams, with a Monday–Friday first shift and on-site work in Andover, MA.

Qualifications

• Bachelor’s degree with 2+ years in regulated environment.
• Experience supporting software/hardware/computer systems in a regulated setting.
• Knowledge of instrument lifecycle processes and data integrity requirements.

Responsibilities

• Support hardware/software installation, configuration, maintenance, troubleshooting, IQ/OQ/PQ support, and data virtualization.
• Provide project management and technical support across instrumentation processes and lifecycle activities.
• Resolve moderately complex instrumentation issues and contribute to related projects with QC/GMP teams.
• Support validation/qualification/upgrade, operation, maintenance, administration, and decommissioning projects at the Andover site.
• Author/review instrument documentation including validation, SOPs, system administration, and data reconciliations.

Skills

Instrumentation lifecycle

Troubleshooting

Project management

Data integrity

System administration

Network technologies

Virtualization

Windows OS

Education

Bachelor's degree + 2+ years

Master's degree + 0+ years

Associate's degree + 6 years

High school diploma + 8 years

Tools

Windows OS

Virtualization

SQL

Job description

Pfizer seeks a System Specialist at the Andover site to support Quality Control and Manufacturing Instrumentation lifecycle activities, including qualification, maintenance, troubleshooting, and data integrity within GMP environments.

You will contribute to validation/upgrade projects and generate documentation while collaborating with QC and GMP teams, with a Monday–Friday first shift and on-site work in Andover, MA.