Teams at MEDVACON Life Sciences LLC

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.

Support Development Business Operations through TMF and contract filing (Apttus, eTMF GDAR), maintain records and inventories, ensure GCP/ICH/GLP compliance, perform data mining, cleansing, statistical and ad-hoc analyses, generate intake and operational reports, and help develop QA, filing, and business continuity processes.

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.