System Specialist

Role: System Specialist supporting instrumentation lifecycle activities within cGMP Quality Control and Manufacturing at Pfizer's Andover site. Responsibilities: provide technical support for hardware/software installation, troubleshooting, validation, upgrades, and decommissioning of lab and manufacturing instruments; author/review validation and maintenance documentation; support system qualification, integrity, and performance projects; and contribute to continuous improvement initiatives. Requirements: bachelor's degree with at least 2 years' experience, or equivalent combination; experience supporting regulated hardware/software and instrument lifecycle processes; strong troubleshooting, project management, and documentation skills. Preferred: experience validating and decommissioning QC/mfg instruments; knowledge of cGMP, Data Integrity, 21 CFR Part 11, ICH guidelines; familiarity with network technologies, virtualization, and Windows troubleshooting. High-Value: cGMP environment, QC/mfg instruments, validation/qualification, instrument lifecycle management, cross-functional support, first shift onsite, occasional off-hours support. Collaboration: work closely with Site Technical Services, QC Lab, and Manufacturing teams. Worksetup: on-premise in Andover, Massachusetts.