About the Role. Pioneer GMP Consulting is seeking a QA Documentation Specialist to support quality operations for a major biopharmaceutical manufacturing client in Worcester, MA. This role focuses on controlled document management within a GMP-regulated environment, including SOP lifecycle management, quality record reviews, QMS workflow oversight, and documentation-related metrics reporting. The ideal candidate is highly detail-oriented, experie...
About the Role. Pioneer GMP Consulting is supporting a major initiative for a large-scale pharmaceutical manufacturer and is seeking a. Project Coordinator. with experience in combination products, medical devices, and pharmaceutical packaging. This role plays an essential part in coordinating cross-functional activities for a combination product and vaccine-related program. The environment is fast-paced, structured, and highly collaborative, req...
Position Summary. Pioneer GMP Consulting is seeking an experienced. Sr. Process Engineer. with 3–7 years of biomanufacturing or pharmaceutical engineering experience to support a global drug manufacturer in Massachusetts. This role focuses on equipment reliability, preventive maintenance execution, troubleshooting, and support for validation and operational readiness activities in a cGMP environment. The ideal candidate brings strong technical pr...
Sr. Process Engineer – Biomanufacturing & Facilities SupportLocation: Massachusetts (On-Site)Duration: 12-Month Project-Based ContractPosition SummaryPioneer GMP Consulting is seeking an experienced Sr. Process Engineer with 3–7 years of biomanufacturing or pharmaceutical engineering experience to support a global drug manufacturer in Massachusetts. This role focuses on equipment reliability, preventive maintenance execution, troubleshooting, and...
Sr. MSAT Engineer – GMP Technical Transfer & Documentation SupportLocation: San Diego, CA (Hybrid)Duration: Fractional / Project-Based ContractPosition SummaryPioneer GMP Consulting is seeking a Sr. MSAT Engineer to support a technical transfer initiative for a biologics manufacturing client. This role blends MSAT expertise with high-level GMP technical writing, focusing on risk assessments, mixing study protocols, and Master Batch Records (MBRs)...
