Sr. MSAT Engineer at Pioneer GMP Consulting

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). The ideal candidate brings strong process knowledge hands-on tech transfer experience and the ability to translate complex manufacturing requirements into clear compliant documentation.Key ResponsibilitiesLead and support tech transfer documentation activities ensuring alignment between sending and receiving sites.Develop and author risk assessments mixing study protocols and Master Batch Records (MBRs) to support GMP manufacturing readiness.Collaborate with Process Development Manufacturing QA and MSAT SMEs to gather technical inputs and consolidate requirements.Apply risk-based science-driven decision-making to documentation and process assessments.Ensure all documents meet GMP data integrity and regulatory expectations including formatting approvals and version control.Support documentation packages required for equipment readiness batch execution and process understanding.Identify documentation gaps and recommend improvements to support a smooth technical transfer.Communicate progress risks and data needs to project leads and cross-functional partners.Required Skills & Experience510 years of MSAT Process Engineering Technical Transfer or Validation experience in GMP biotech or pharmaceutical manufacturing.Strong experience authoring or reviewing:Risk assessments (FMEA hazard analyses etc.)Study protocols (mixing studies process studies)MBRs / EBR contentTechnical reports and GMP documentsDeep understanding of GMP data integrity and GDocP.Demonstrated experience supporting or leading technical transfer between internal teams or CDMOs.Ability to interpret process requirements equipment capability and manufacturing constraints.Excellent written communication skills with the ability to simplify complex technical concepts. Preferred QualificationsExperience in biologics cell culture or aseptic manufacturing.Prior work in CDMO environments or external collaboration models.Knowledge of risk-based frameworks (ICH Q9) scale-up considerations and process characterization.Compensation & BenefitsCompetitive hourly/salary rates commensurate with experience. Travel and per diem allowances may apply depending on assignment.Equal Opportunity EmployerPioneer GMP Consulting is an Equal Opportunity Employer. We do not discriminate based on race color religion sex sexual orientation gender identity national origin age disability veteran status or any other protected category under applicable law. Key Skills ASP.NET,Health Education,Fashion Designing,Fiber,Investigation Employment Type : Full Time Experience: years Vacancy: 1