Senior Instrument Systems Architect

Pfizer; Andover (MA); On-site; USD 99,000 - 165,000; Full time

Benefits offered by this job

401(k) with Pfizer matching

Paid vacation

Health benefits

Job summary

Pfizer in Andover, MA is seeking a Senior System Specialist to support instrument lifecycle activities across Quality Control and GMP manufacturing suites. The role includes hardware/software installation, troubleshooting, and data integrity tasks within a regulated environment.

You will lead project management, validation/upgrade efforts, and documentation development while collaborating with QC and GMP teams to ensure reliability and compliant operations.

Qualifications

• Bachelor's degree with 4+ years experience in a regulated environment.
• Master's degree with 2+ years experience or PhD with 0+ years experience.
• Associate's degree with 8 years experience or a high school diploma with 10 years experience.

Responsibilities

• Support instrument lifecycle processes across Quality Control and Manufacturing instrumentation.
• Lead projects, validation/qualification/upgrade activities.
• Prepare and review validation and instrument documentation, Change Controls and investigations.
• Provide incident response, data integrity assessments, and decommissioning support.

Skills

Instrumentation lifecycle experience

Regulated environment experience

Project management

Education

Bachelor's degree with 4+ years experience

Master's degree with 2+ years experience

PhD with 0+ years experience

Associate's degree with 8 years experience

High school diploma with 10 years experience

Tools

IQ/OQ/PQ

Virtual Network (VLAN)

Network security protocols

virtualization systems

Windows operating system troubleshooting

Job description

Pfizer in Andover, MA is seeking a Senior System Specialist to support instrument lifecycle activities across Quality Control and GMP manufacturing suites. The role includes hardware/software installation, troubleshooting, and data integrity tasks within a regulated environment.

You will lead project management, validation/upgrade efforts, and documentation development while collaborating with QC and GMP teams to ensure reliability and compliant operations.