Syner-G

Sr. Project Manager

Boston, Massachusetts, United States · Senior

Sponsorship not specified$10k-$15kDetected 1 day ago

Project ManagementGMPCRISPRMedical DevicesLeadershipCommunicationProblem Solving

About the role

We are seeking a highly experienced Sr.
Project Manager to lead the planning, implementation, and execution of an integrated Verification and Commissioning & Qualification (C&Q) Program for large-scale GMP-regulated capital projects.
Travel to client sites will be required up to 100%, depending on project needs and client expectations.

Lead the development and execution of an integrated Verification and C&Q Program across the full project lifecycle, from design through operational handover.
Establish and implement project-specific verification strategies aligned with ASTM E2500 principles and industry best practices.
Manage overall C&Q scope, budget, schedule, resource planning, and project risks.
Develop detailed C&Q execution plans, staffing strategies, milestone schedules, and performance metrics.
Lead, mentor, and develop multidisciplinary C&Q teams supporting project execution.
Manage day-to-day team activities, task assignments, priorities, and performance.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Bachelor's Degree in Engineering, Life Sciences, or a related technical discipline.
Experience managing FAT, SAT, commissioning, qualification, verification testing, and system turnover activities.
Working knowledge of facility, utility, process, automation, and manufacturing systems commonly deployed within GMP environments.
Experience managing budgets, resource plans, schedules, and contract service providers.
Familiarity with GMP documentation practices, quality systems, change controls, deviations, CAPAs, and validation lifecycle requirements.
Strong understanding of GMP regulations, commissioning, qualification, validation, and verification practices.
Deep knowledge of ASTM E2500 and lifecycle-based validation methodologies.
While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reach with hands and arms; talk and listen.
The employee is frequently required to walk and sit, as well as to lift and carry objects such as books and files weighing up to 25 pounds.
The employee is occasionally required to stand, stoop, or kneel.

Advanced degree, PMP certification, or equivalent professional certification preferred.
Experience with electronic validation systems and digital quality platforms, including Kneat, ValGenesis, or similar platforms, is preferred.

A career here is life-enhancing.
Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact.
For more information, visit www.Synergbiopharma.com

This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities.

This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities.
Specific vision abilities required by this position include close vision and the ability to adjust focus.

We define total rewards as compensation, benefits, remote work/flexibility, development, recognition, and our culture with programs that support each of our reward pillars.

This listing is sourced directly from Syner-G's careers page and normalized into a canonical job model.