Jobs at Syner-G

Manage concurrent facilities, engineering, maintenance, utility, infrastructure, and site services projects from initiation through closeout. Responsibilities include planning scope, schedules, budgets, resources, risks, procurement, contractors, shutdowns, installations, commissioning, qualification, turnover, and stakeholder communications. The role coordinates cross-functional teams in regulated pharmaceutical, biotechnology, medical device, and advanced manufacturing environments while ensuring GMP, safety, quality, and site compliance.

The Senior Program Manager will lead facility readiness and laboratory relocation projects in regulated life sciences environments. Responsibilities include coordinating facility build-outs, equipment moves, utility readiness, commissioning, qualification, validation, construction activities, stakeholder communication, schedules, risks, deviations, and turnover documentation. The role works with engineering, facilities, quality, EHS, IT, operations, CQV teams, contractors, and vendors to deliver safe, compliant, and timely project outcomes.

Leads strategic client initiatives and complex capital projects from design through construction, commissioning, and handover. Establishes governance, portfolio reporting, stakeholder engagement, risk management, and executive communication processes. Acts as owner’s representative, coordinates contractors and technical teams, reviews design and construction documentation, manages site activities, and supports startup, turnover, and operational readiness. The role requires extensive capital project experience, strong project controls expertise, and frequent travel to client sites.

Provides coordination and administrative support for construction and maintenance projects, emphasizing health and safety compliance. Responsibilities include organizing pre-construction meetings, maintaining schedules and safety documentation, reviewing contractor safety plans, tracking hazards and corrective actions, compiling safety metrics, supporting incident investigations and inspections, coordinating stakeholders, and assisting with contracts, purchase orders, invoicing, onboarding, and project controls.

Leads cross-functional strategic, transformation, integration, operational improvement, and client-focused projects across the biopharmaceutical and CMO/CDMO environment. Responsibilities include project planning, timeline and budget management, risk mitigation, resource alignment, stakeholder coordination, governance, executive reporting, and continuous improvement. The role supports initiatives such as mergers and acquisitions, client onboarding, strategic partnerships, and organizational change while ensuring projects remain aligned with business objectives and client commitments.