Teams at MEDVACON Life Sciences LLC

Lead cross-functional pharma/cell therapy projects: define scope, timelines, resources; manage budget/schedule changes; run team meetings; track risks and issues; provide status dashboards; maintain project management processes; support change management and continuous improvement.

Multiple GMP Quality Control roles supporting a gene therapy client in Lexington, MA, including method validation, microbiology, sample management, LIMS administration, QC planning, and supervisory positions. Candidates must have prior cGMP/QC experience and US work authorization. Roles include second-shift openings and several specialized QC functions.

Lead and manage pharma portfolio projects: define scope, timelines, resources; control scope/schedule/budget changes; run team meetings; identify and mitigate risks; produce status trackers/dashboards; maintain project management processes/templates; support change management and continuous improvement; escalate issues as needed.