Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Syner-G BioPharma Group

Senior Project Manager

Syner-G BioPharma Group

Sr. Project Manager overseeing HVAC, facility, and validation-focused initiatives within GMP life sciences environments.

Posted 6/30/2026full-timeRemote • 🇺🇸 United StatesSeniorWebsite

Tech Stack

Tools & technologies
AirflowPMP

About the role

Key responsibilities & impact
  • Provide strategic leadership and oversight for projects spanning HVAC systems, facility infrastructure, commissioning, qualification, and operational readiness
  • Lead HVAC project execution activities across pharmaceutical manufacturing, laboratory, and support areas
  • Develop and manage project plans, schedules, budgets, resource strategies, and risk mitigation activities across multiple workstreams
  • Coordinate HVAC scope with construction, CQV, automation, facilities, and manufacturing teams
  • Oversee cleanroom implementation including airflow design, pressurization cascades, and environmental control strategies to meet GMP requirements
  • Manage contractors, vendors, schedules, field execution, and punch list activities through project completion
  • Drive HVAC startup, commissioning, qualification (IQ/OQ/PQ), and validation activities in alignment with CQV strategies
  • Support cleanroom and GMP facility readiness activities, including environmental monitoring alignment and operational setup
  • Perform and lead field walkdowns, system inspections, and issue resolution for HVAC and facility systems
  • Ensure delivery of key milestones, commissioning deliverables, validation packages, and turnover documentation
  • Guide development and execution of commissioning plans, qualification protocols, and turnover packages
  • Partner with CQV teams to ensure design and user requirements translate effectively into validation documentation and execution
  • Ensure alignment with engineering standards, safety requirements, and GMP expectations
  • Identify risks and drive mitigation strategies related to HVAC performance, contamination control, and facility operations
  • Track project deliverables, budgets, timelines, KPIs, and action items across all workstreams
  • Facilitate cross-functional meetings and communicate project status to leadership and stakeholders
  • Coordinate change controls, deviations, CAPAs, and documentation within quality systems (eQMS)
  • Support operational readiness and transition from construction and CQV into facility operations
  • Utilize systems such as CMMS, eQMS, LMS, and digital validation platforms; experience with KNEAT is a plus
  • Mentor and support project managers, engineers, and coordinators to ensure high quality execution and professional development

Requirements

What you’ll need
  • Bachelor’s Degree in Engineering, Life Sciences, or a related technical field. A Master’s degree or PMP certification is a plus.
  • 10–15 years of experience in GMP regulated environments (biotech, pharmaceutical, cell/gene therapy, or medical device)
  • Strong experience with HVAC systems, cleanroom environments, and facility utilities (e.g., chilled water, steam, controls)
  • Experience leading HVAC-focused projects and managing multiple concurrent initiatives
  • Experience with CQV lifecycle activities including commissioning and qualification of HVAC systems
  • Experience with cleanroom standards, environmental monitoring, and contamination control principles
  • Experience conducting or overseeing field walkdowns, readiness checks, and operational verification
  • Familiarity with BMS/EMS systems and HVAC control strategies
  • Experience with GMP documentation, change control, deviations, and validation packages
  • Familiarity with CMMS, eQMS, LMS, or similar regulated systems
  • Experience with KNEAT or digital validation platforms is a plus.

Benefits

Comp & perks
  • market competitive base salary and annual incentive plan
  • robust benefit offerings
  • ongoing recognition and career development opportunities
  • generous flexible paid time off program
  • company-paid holidays
  • flexible working hours
  • fully remote work options for most positions

ATS Keywords

✓ Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
HVAC System DesignProject PlanningRisk MitigationEnvironmental MonitoringContamination ControlField WalkdownsValidation DocumentationChange ControlCommissioning PlansQualification Protocols
Soft Skills
LeadershipCommunicationMentoringCollaborationProblem-Solving
Certifications
Bachelor’s Degree in EngineeringMaster’s DegreePMP Certification