Role: Multiple Program Manager & Project Manager
Industry: Healthcare | Pharmaceuticals | Life Sciences | Medical Devices
Client: Thermo Fisher Scientific
Employment Type: Long-Term Contract
Work Arrangement: 100% Remote (base location: Greenville, SC Occasional Travel once in quarter expense will be covered)
Start Date: ASAP
We are seeking experienced Program Managers and Project Managers with strong backgrounds in healthcare, pharmaceutical manufacturing, life sciences, or medical devices for multiple long-term contract opportunities supporting Thermo Fisher Scientific.
Candidates should have experience managing complex projects in regulated environments, coordinating cross-functional teams, managing project risks and deliverables, and ensuring compliance with applicable quality and regulatory requirements.
Candidates who prefer remote opportunities are welcome to express interest.
#Role 1:
Program Manager – GxP CAPA Remediation
Long‑Term Contract
Lead coordination and execution of CAPA remediation workstreams in a regulated pharma manufacturing environment. This is a domain‑focused PM role (not IT) working closely with Manufacturing, Quality, Validation & MSAT.
Key Points:
* Manage CAPA/remediation workstreams end‑to‑end
* Track actions, dependencies, risks & decisions
* Facilitate working sessions & follow‑ups
* Strong GxP, CAPA, quality‑system experience required
#Role 2:
MES IT Program Manager – Life Sciences
Long‑Term Contract
Lead strategy, planning & delivery of MES programs across pharma/biotech sites. Drive multi‑site deployments and ensure full GxP/GMP/CSV/data‑integrity compliance.
Highlights:
* Own MES roadmap & governance
* Lead global/regional MES deployments
* Align MES with Manufacturing, Quality, Engineering, Automation & IT
* Strong stakeholder & vendor management
#Role 3:
MES Project Manager
Long‑Term Contract
Lead full lifecycle MES projects — design, configuration, testing, validation, deployment & operational handover.
Highlights:
* Manage MES scope, schedules, budgets & risks
* Lead workstreams: EBR, EWI, equipment integration, genealogy, exceptions
* Ensure GxP/GMP/CSV/data‑integrity compliance
* Experience with PAS‑X, Opcenter, PharmaSuite, Syncade preferred
