Senior Project Manager (QC Analytical - Pharmaceutical)

Cumming Group•Devens, MA

8d•$127,300 - $178,233•Onsite

About The Position

At Cumming Group, you will work on some of the world's most exciting projects in a dynamic environment where your success is measured by the impact you make. We are one of the fastest-growing project and cost management consultancies in the United States, as reflected in our top 10 rankings in ENR. With over 60 offices globally, an extremely diverse project portfolio, and double-digit year-over-year revenue growth, the opportunities to make your mark are limitless! This role involves supporting project management for QC project meetings, managing KPIs, tracking timelines, identifying and escalating risks, and acting as a subject matter expert in bioanalytical techniques. The position also requires developing and executing methods, protocols, and reports aligned with regulatory guidelines.

Requirements

Bachelor’s degree or equivalent required, preferably in science.
Scientific knowledge with a broad range of bioanalytical techniques (cell-based assays, ELISA, qPCR, flow cytometry) and deep expertise with the characterization, validation, and transfer of bioanalytical methods.

Nice To Haves

Advanced degree preferred.

Responsibilities

Effectively support project management for QC project meetings, including the scheduling of meetings, preparation of agendas, development of meeting minutes, and follow-up on action items.
Manage and report Key Performance Indicators (KPIs), including timelines, milestones, and escalations.
Track timeline elements to ensure that functional deliverables are completed on time and according to relevant quality standards.
Proactively identify, communicate, and escalate risks and decisions to site leadership.
Work with team members, project leader and Subject Matter Experts (SMEs) to develop contingency plans when required.
Subject matter expert in bioanalytical techniques (e.g., cell-based assays, ELISA, qPCR, flow cytometry) leading method transfer/validation and routine testing of in-process, final product, and stability samples.
SME for training and mentoring team on multiple complex QC test methods, processes, and procedures.
Independently develop, write, and execute methods, protocols, reports, and other related documents aligned with regulatory and corporate guidelines.
Manage and monitor team members' activity in alignment with organizational goals.
Delegate providing clear instructions and ongoing feedback.
Monitor metrics and course correct as necessary while holding self and others accountable.
Provide feedback to senior leaders and clearly communicate organizational direction to team members.
Build relationships with key internal resources (peers, direct reports, and senior leaders).