Jobs at PerkinElmer

Senior leader responsible for directing mega-capital life sciences projects (> $200M TIC) from concept through operations. Provide strategic governance, risk mitigation, financial oversight, cross-functional integration (engineering, quality, regulatory), and mentor project teams. Ensure compliance with GMP/FDA/ISO/EHS standards, lead portfolio planning, and drive operational readiness, cost optimization, and continuous improvement across multi-geography programs.

Lead project controls tasks for biomanufacturing projects including schedule, cost, and performance management. Develop integrated schedules, budgets, variance and risk analyses, dashboards and monthly status reports. Collaborate with clients and cross-functional teams, maintain project controls systems, and support CAPEX, validation, and operational readiness activities.

Lead and oversee capital life‑sciences projects from design through startup, managing scope, budget, schedule, risk, and regulatory compliance. Serve as the owner's representative, mentor project teams, coordinate cross‑functional and EPC/EPCM partners, and drive continuous improvement and operational readiness.

Provides remote technical support for PerkinElmer atomic spectroscopy instruments across North America. Diagnoses complex hardware, software, and application issues; guides customers and field engineers through repairs; identifies root causes, parts, and corrective actions; documents service activity; supports first-time fixes, training, mentoring, technical communications, and operational improvements. Requires expert repair-level experience with atomic spectroscopy platforms, including at least two of AA, ICP-OES, and ICP-MS.

Lead marketing strategy and execution for Project Farma, driving lead generation, ABM, digital channels, content, PR, events, and metrics. Manage budget, mentor team, collaborate with business development and sales, and use data to optimize campaigns and growth.

Lead Automation Engineer for MES and digital systems designing, implementing, validating, and supporting MES/DCS/PLC/SCADA architectures for GMP biologics/pharma facilities. Author URS/FRS/DS, lead validation (FAT/SAT/IQ/OQ/PQ) to GAMP5 and 21 CFR Part 11, integrate ERP/LIMS/CMMS, support commissioning, investigations, and client-facing delivery.