W2 ONLY - Need MES Program Manager- Foster City, CA - onsite

Application Portfolio ScopePrimary ResponsibilityDomainRepresentative SystemsRegulatory ContextClinicaleTMF, CTMS, EDC (Medidata/Veeva), IRT/RTSM, Safety/Pharmacovigilance (ArgOracle), eCOA/ePROICH E6 (R2) Google Cloud Platform, 21 CFR Part 11, EU Annex 11QualityEQMS (Veeva Quality One / Master Control), LIMS, Batch Record (EBR/MBR), QMS, Deviation & CAPA, Change Control21 CFR Part 11, ICH Q10, ISO 13485, EU GMP Annex 11R&D / CMCELN (Lab Archives / Benchling), SDMS, Formulation & Stability, Assa

Title: On Site MES IT Coordinator Location: Cincinnati, OH (Remote with travel required) Description: Department:Manufacturing Execution Systems (MES) Center of Excellence (CoE) The Site MES IT Coordinator serves as the primary site-level IT and MES liaison responsible for coordinating Manufacturing Execution System (MES) implementation, deployment, and ongoing operational support across manufacturing facilities. This role acts as the critical interface between site operations, Quality, MS

Job Title: MES Functional Consultant (Rockwell FactoryTalk PharmaSuite) Location: Remote Job Type: Contract / Full-Time Experience: 8+ Years Role Overview We are seeking an experienced MES Functional Consultant with strong hands-on expertise in Rockwell FactoryTalk PharmaSuite to support pharmaceutical manufacturing operations. The role involves configuring, maintaining, and enhancing the MES platform while working closely with manufacturing, quality, and IT teams in a GMP-regulated environm

Title: Project Manager - MES (Medical Devices / Life Sciences) Location: Pittsburgh, PA (Remote) Experience: 10+ years About the Role We are seeking an experienced Project Manager (PM) to lead the implementation and delivery of Manufacturing Execution Systems (MES) within a highly regulated medical devices/life sciences environment. This role requires strong technical expertise, regulatory knowledge, and leadership capabilities to manage cross-functional teams and ensure compliance with FDA a