Senior System Specialist

Role: Senior System Specialist supporting instrumentation lifecycle management at Pfizer's Andover site, focusing on Quality Control and GMP manufacturing instruments. Responsibilities: provide technical support for hardware/software installation, qualification, upgrades, operation, troubleshooting, reliability, and decommissioning of cGMP instruments; lead validation, system administration, and continuous improvement projects; author and review validation and system documentation; collaborate with vendors and internal teams to ensure compliance with cGMP, Data Integrity, and 21 CFR Part 11 standards. Requirements: bachelor's degree with ≥4 years experience, or equivalent, supporting instrument systems in regulated environments; proficient in hardware, software, network technologies, and troubleshooting in cGMP settings. Preferred: experience validating and decommissioning QC/manufacturing instruments, knowledge of network security, virtualization, and regulatory standards. High-Value: emphasis on instrument lifecycle, cGMP compliance, validation, and system troubleshooting in a pharmaceutical manufacturing setting. Work setup: on-premise, first shift, with occasional off-hour support and some travel.