John Kayati Email & Phone Number
Sr. Director, Quality Assurance, GMP Manufacturing @ Gemma Biotherapeutics
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John Kayati Location
- Pottstown, PA, US
John Kayati Work
- 2024 -now Sr. Director, Quality Assurance, GMP Manufacturing @
- 2022 -2025 Director, Quality Assurance, GMP Manufacturing @ Gene Therapy Program, Perelman Scholl of Medicine
- 2016 -2022 QA Manager, CMO @
- 2014 -2016 Quality Assurance Manager @
- 2012 -2014 Manager Quality Assurance @ Nuron Biotech Inc
- 2007 -2011 Lead Lab Supervisor, Quality Operations @
- 2000 -2007 Sr. Manufacturing Supervisor, Merck Manufacturing Division @
- 1998 -2000 BTMC Biotechnician (Fermentation), Merck Manufacturing Division @ Merck
John Kayati Education
- Rutgers University
B.A (Biology)
1981-1986 - Paul VI High School, Haddonfield NJ
Diploma (College prepatory - life sciences)
1977-1981
John Kayati Skills
- Biopharmaceutical (Vaccine Manufacturing) Experience
- Laboratory Operations (Analytical Testing)
- Quality Control/Quality Assurnce
- Regulatory Compliance
- Quality Management Systems
- Continuous Improvement
- Lean Manufacturing/Six Sigma Methodologies
- Warehouse Management/Inventory Control
- Technical Writing/Deviation Management
- Raw Material (Receipt, Sampling, Dispensing, Testing)
- Environmental Monitoring
- Personnel Management/Leadership/Training
- Scheduling & Planning
- Project Management
- Data Analysis/Batch Record Review & Approval
- Process Scheduler
- Laboratory
- Project Planning
- Testing
- Quality System
- GMP
- Quality Assurance
- Sop
- GLP
- Change Control
- V&V
- Quality Control
- Pharmaceutical Industry
- Validation
- FDA
- CAPA
- Biotechnology
- 21 CFR Part 11
- Six Sigma
- Pharmaceutics
- U.S. Food and Drug Administration (FDA)
- Corrective and Preventive Action (CAPA)
- Standard Operating Procedure (SOP)
- Good Laboratory Practice (GLP)
- Quality Management
- Dispensing
- Good Laboratory Practice Glp
- Biopharmaceutical
- Laboratory Operations Analytical Testing
- Scheduling and Planning
- Warehouse
- Corrective and Preventive Action Capa
- Personnel
- Biopharmaceutical Vaccine Manufacturing Experience
- Laboratory Operations
- u.s. Food and Drug Administration Fda
- Quality Control/Quality
- Sampling
- Data Analysis/Batch Record Review and Approval
- Raw Material Receipt
- Lean Manufacturing/Six
- Data Analysis/Batch
- Standard Operating Procedure Sop
- Technical
- Standard Operating Procedure
- u.s. Food and Drug Administration
- Good Laboratory Practice
- Corrective and Preventive Action
- Biopharmaceutical Experience
- Raw Material
John Kayati Summary
- John Kayati, based in Pottstown, PA, US, is currently a Sr. Director, Quality Assurance, GMP Manufacturing at GEMMA Biotherapeutics. John Kayati brings experience from previous roles at Gene Therapy Program, Perelman Scholl of Medicine, Teva Pharmaceuticals, Janssen, Pharmaceutical Companies of Johnson and Johnson and Nuron Biotech Inc. John Kayati holds a 1981 - 1986 B.A in Biology @ Rutgers University. With a robust skill set that includes Biopharmaceutical (Vaccine Manufacturing) Experience, Laboratory Operations (Analytical Testing), Quality Control/Quality Assurnce, Regulatory Compliance, Quality Management Systems and more. John Kayati has 2 emails and 3 mobile phone numbers on RocketReach.
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